Report date: Nov 6,2024
Conflict count: 361874
Publisher: Wiley (Blackwell Publishing)
Title count: 475
Conflict count: 16773


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Created: 2023-11-20 07:01:12
ConfID: 7037033
CauseID: 1597931110
OtherID: 5360
JT: Annals of Human Genetics
MD: STEPHENSON,61,6,553,1997,An Electronic Companion to Genetics. Workbook by Philip Anderson and Barry Ganetzky. New York: Cogito Learning Media, Inc. £19.53. CD ROM for Macintosh/PCs and 304 page companion book.
DOI: 10.1017/S000348009722659X(Journal) (7037033-N)
DOI: 10.1111/j.1469-1809.1997.ahg616_0553_2.x(Journal)
==========================================================

Created: 2023-11-20 07:00:58
ConfID: 7037032
CauseID: 1597931054
OtherID: 5360
JT: Annals of Human Genetics
MD: SHEER,61,5,463,1997,Genetics of Human Neoplasia. Volume 3 of Advances in Genome Biology. Edited by Ram S. Verma. JAI Press, London. 1995. 2 Vols: Pp. 232 & Pp. 248. £125.00 (US$195.00). ISBN: 1 55938 835 8.
DOI: 10.1017/S0003480097256411(Journal) (7037032-N)
DOI: 10.1111/j.1469-1809.1997.ahg615_0463_5.x(Journal)
==========================================================

Created: 2023-11-20 07:08:17
ConfID: 7037038
CauseID: 1597932719
OtherID: 33686200
JT: Annals of Human Genetics
MD: BOURGAIN,66,1,99,2002,Missing data in haplotype analysis: a study on the MILC method
DOI: 10.1017/S000348000100896X(Journal) (7037038-N)
DOI: 10.1046/j.1469-1809.2002.6610099.x(Journal)
==========================================================

Created: 2023-11-20 07:00:58
ConfID: 7037031
CauseID: 1597931054
OtherID: 5355
JT: Annals of Human Genetics
MD: DAY,61,5,463,1997,Mutation Detection. By Richard G. H. Cotton. Oxford: Oxford University Press. 1997. Pp. 198. £22.50 (paperback).
DOI: 10.1017/S0003480097246415(Journal) (7037031-N)
DOI: 10.1111/j.1469-1809.1997.ahg615_0463_4.x(Journal)
==========================================================

Created: 2023-11-20 07:00:58
ConfID: 7037030
CauseID: 1597931054
OtherID: 5355
JT: Annals of Human Genetics
MD: MORRISON,61,5,463,1997,Does It Run in the Family? A Consumer's Guide to DNA Testing for Genetic Disorders. By Doris Teichler Zallen. New Brunswick, NJ, London: Rutgers University Press, 1997. Pp. 201.
DOI: 10.1017/S0003480097226412(Journal) (7037030-N)
DOI: 10.1111/j.1469-1809.1997.ahg615_0463_2.x(Journal)
==========================================================

Created: 2023-11-20 07:00:54
ConfID: 7037029
CauseID: 1597931037
OtherID: 5360
JT: Annals of Human Genetics
MD: STEPHENSON,61,3,283,1997,Genetics Variants and Strains of the Laboratory Mouse. Third edition. Edited by M. F. Lyon, S. Rastan and S. D. M. Brown. Oxford: Oxford University Press. 1996. Volumes 1 and 2 pp. 1807. £150.
DOI: 10.1017/S0003480097226229(Journal) (7037029-N)
DOI: 10.1111/j.1469-1809.1997.ahg613_0283_2.x(Journal)
==========================================================

Created: 2023-11-20 07:00:49
ConfID: 7037028
CauseID: 1597931015
OtherID: 5355
JT: Annals of Human Genetics
MD: WALSHE,61,2,173,1997,Wilson's Disease, vol. 30 in the series Major Problems in Neurology. By Tjaard Hoogenraad. London, Philadelphia, Toronto, Sydney, Tokyo: W. B. Saunders. Co Ltd. Pp. 209. £45.00.
DOI: 10.1017/S0003480097226072(Journal) (7037028-N)
DOI: 10.1111/j.1469-1809.1997.ahg612_0173_2.x(Journal)
==========================================================

Created: 2023-11-20 07:27:40
ConfID: 7037048
CauseID: 1597937184
OtherID: 5355
JT: Annals of Human Genetics
MD: SMITH,62,4,361,1998,Lancelot Hogben, Scientific Humanist: An unauthorised autobiography. Edited by ADRIAN and ANNE HOGBEN. Rendlesham, Suffolk: Merlin Press. 1998. Pp. 254. £14.95.
DOI: 10.1017/S0003480098227035(Journal) (7037048-N)
DOI: 10.1111/j.1469-1809.1998.ahg624_0361_2.x(Journal)
==========================================================

Created: 2023-11-20 07:23:15
ConfID: 7037043
CauseID: 1597936055
OtherID: 5356
JT: Annals of Human Genetics
MD: GARDINER,63,3,273,1999,Genetics of Focal Epilepsies: Clinical Aspects and Molecular Biology. Current Problems in Epilepsy: 13. Edited by S. F. BERKOVIC, P. GENTON, E. HIRSCH and F. PICARD. London: John Libbey. 1999. Pp. 286. £59.00, US $103.00.
DOI: 10.1017/S0003480099237530(Journal) (7037043-N)
DOI: 10.1111/j.1469-1809.1999.ahg633_0273_3.x(Journal)
==========================================================

Created: 2023-11-20 07:23:15
ConfID: 7037042
CauseID: 1597936055
OtherID: 5356
JT: Annals of Human Genetics
MD: HUMPHRIES,63,3,273,1999,Evolution in Health and Disease. Edited by S. C. STEARNS. Oxford: Oxford University Press. 1999. Pp. 328. £23.50 (paperback).
DOI: 10.1017/S0003480099227534(Journal) (7037042-N)
DOI: 10.1111/j.1469-1809.1999.ahg633_0273_2.x(Journal)
==========================================================

Created: 2023-11-20 07:27:21
ConfID: 7037047
CauseID: 1597937088
OtherID: 5355
JT: Annals of Human Genetics
MD: HARDY,62,1,93,1998,Genetic Control of Heart Development. Third Report of the Human Frontier Science Program, Workshop III, Strasbourg, 1997. Edited by E. N. Olson, R. P. Harvey, R. A. Schulz and J. S. Altman. Pp. 189 (paperback).
DOI: 10.1017/S0003480098226704(Journal) (7037047-N)
DOI: 10.1111/j.1469-1809.1998.ahg621_0093_2.x(Journal)
==========================================================

Created: 2023-11-20 07:23:51
ConfID: 7037045
CauseID: 1597936204
OtherID: 5356
JT: Annals of Human Genetics
MD: SMITH,64,1,89,2000,Lionel Sharples Penrose: a Biography. By M. SMITH. Obtainable from The Lavenham Press, Water St., Lavenham, Sudbury CO10 9RN. £9.95, p+p £1.
DOI: 10.1017/S0003480000247891(Journal) (7037045-N)
DOI: 10.1111/j.1469-1809.2000.ahg641_0089_4.x(Journal)
==========================================================

Created: 2023-11-20 07:23:51
ConfID: 7037044
CauseID: 1597936204
OtherID: 5356
JT: Annals of Human Genetics
MD: WATERWORTH,64,1,89,2000,Analysis of Human Genetic Linkage. By J. OTT. Baltimore, London: Johns Hopkins University Press. 1999 (3rd edition). Pp. 382. £38.00.
DOI: 10.1017/S0003480000227899(Journal) (7037044-N)
DOI: 10.1111/j.1469-1809.2000.ahg641_0089_2.x(Journal)
==========================================================

Created: 2023-11-20 07:27:40
ConfID: 7037160
CauseID: 1597937176
OtherID: 5355
JT: Annals of Human Genetics
MD: BURNS,62,4,361,1998,Protein Dysfunction in Human Genetic Disease. Edited by D. M. SWALLOW and Y. H. EDWARDS. Oxford: Bios Scientific Publishers. 1997. Pp. 258. £65.00.
DOI: 10.1017/S0003480098217039(Journal) (7037160-N)
DOI: 10.1046/j.1469-1809.1998.62403611.x(Journal)
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Created: 2023-11-20 07:27:29
ConfID: 7037155
CauseID: 1597937119
OtherID: 5355
JT: Annals of Human Genetics
MD: PALIN,62,5,465,1998,Telomeres and Telomerase. Edited by D. J. CHADWICK and G. CARDEW. Chichester: John Wiley and Sons, 1997. Pp. 238.
DOI: 10.1017/S0003480098217155(Journal) (7037155-N)
DOI: 10.1046/j.1469-1809.1998.62504651.x(Journal)
==========================================================

Created: 2023-11-20 07:27:21
ConfID: 7037154
CauseID: 1597937087
OtherID: 5355
JT: Annals of Human Genetics
MD: ,62,3,189,1998,Lionel Penrose FRS, 1898–1972
DOI: 10.1017/S0003480098009671(Journal) (7037154-N)
DOI: 10.1046/j.1469-1809.1998.6230189.x(Journal)
==========================================================

Created: 2023-11-20 07:27:31
ConfID: 7037159
CauseID: 1597937140
OtherID: 5355
JT: Annals of Human Genetics
MD: DE ANDRADE,62,6,505,1998,Segregation analysis of squamous cell carcinoma of the head and neck: evidence for a major gene determining risk
DOI: 10.1017/S0003480099007204(Journal) (7037159-N)
DOI: 10.1046/j.1469-1809.1998.6260505.x(Journal)
==========================================================

Created: 2023-11-20 07:27:31
ConfID: 7037158
CauseID: 1597937140
OtherID: 5355
JT: Annals of Human Genetics
MD: De STEFANO,62,6,481,1998,Linkage disequilibrium at the cystathionine β synthase (CBS) locus and the association between genetic variation at the CBS locus and plasma levels of homocysteine
DOI: 10.1017/S0003480099007186(Journal) (7037158-N)
DOI: 10.1046/j.1469-1809.1998.6260481.x(Journal)
==========================================================

Created: 2023-11-20 07:27:29
ConfID: 7037157
CauseID: 1597937120
OtherID: 5355
JT: Annals of Human Genetics
MD: EDWARDS,62,5,453,1998,Fisher, Haldane and Wright in the decade 1922–1932.
DOI: 10.1017/S0003480098277141(Journal) (7037157-N)
DOI: 10.1111/j.1469-1809.1998.ahg625_0453_7.x(Journal)
==========================================================

Created: 2023-11-20 07:27:29
ConfID: 7037156
CauseID: 1597937119
OtherID: 5355
JT: Annals of Human Genetics
MD: AL TALABANI,62,5,411,1998,Major congenital malformations in United Arab Emirates (UAE): need for genetic counselling
DOI: 10.1017/S0003480098007118(Journal) (7037156-N)
DOI: 10.1046/j.1469-1809.1998.6250411.x(Journal)
==========================================================

Created: 2023-11-20 07:22:52
ConfID: 7037147
CauseID: 1597935957
OtherID: 5355
JT: Annals of Human Genetics
MD: ,63,2,119,1999,Abstracts
DOI: 10.1017/S0003480098009981(Journal) (7037147-N)
DOI: 10.1046/j.1469-1809.1999.6320119.x(Journal)
==========================================================

Created: 2023-11-20 07:22:29
ConfID: 7037145
CauseID: 1597935851
OtherID: 5356
JT: Annals of Human Genetics
MD: JIMENEZ,63,4,377,1999,In Situ Hybridization: A Practical Approach. 2nd Edition. Edited by D. G. WILKINSON (Series Editor: B. D. Hames). Oxford: Oxford University Press. 1998. Pp. 224. £29.95 (paperback). (Hard covers £65.00.)
DOI: 10.1017/S0003480099237645(Journal) (7037145-N)
DOI: 10.1111/j.1469-1809.1999.ahg634_0377_3.x(Journal)
==========================================================

Created: 2023-11-20 07:22:29
ConfID: 7037144
CauseID: 1597935851
OtherID: 5356
JT: Annals of Human Genetics
MD: HALL,63,4,377,1999,The Principles of Clinical Cytogenetics. Edited by S. L. GERSEN and M. B. KEAGLE. Totowa, NJ: Humana Press. 1999. Pp. 558. $79.50.
DOI: 10.1017/S0003480099227649(Journal) (7037144-N)
DOI: 10.1111/j.1469-1809.1999.ahg634_0377_2.x(Journal)
==========================================================

Created: 2023-11-20 07:24:32
ConfID: 7037151
CauseID: 1597936351
OtherID: 33686200
JT: Annals of Human Genetics
MD: SUN,64,6,555,2000,Transmission/disequilibrium tests for quantitative traits
DOI: 10.1046/j.1469-1809.2000.6460555.x(Journal) (7037151-N)
DOI: 10.1017/S000348000000840X(Journal)
==========================================================

Created: 2023-11-20 07:24:32
ConfID: 7037150
CauseID: 1597936351
OtherID: 33686200
JT: Annals of Human Genetics
MD: ENNIS,64,6,513,2000,Allelic association in the FRAX region
DOI: 10.1046/j.1469-1809.2000.6460513.x(Journal) (7037150-N)
DOI: 10.1017/S000348000000837X(Journal)
==========================================================

Created: 2023-11-20 07:23:51
ConfID: 7037149
CauseID: 1597936203
OtherID: 5356
JT: Annals of Human Genetics
MD: VERMA,64,1,89,2000,In Situ Hybridization: Principles and Practice. Edited by J. M. POLAK and J. O'D. MCGEE. Oxford Medical Publications. Oxford: Oxford University Press. 1998 (2nd Edition). Pp. 212. £39.95.
DOI: 10.1017/S0003480000217892(Journal) (7037149-N)
DOI: 10.1046/j.1469-1809.2000.64100891.x(Journal)
==========================================================

Created: 2023-11-20 07:23:14
ConfID: 7037148
CauseID: 1597936045
OtherID: 5356
JT: Annals of Human Genetics
MD: MALLET,63,3,273,1999,Molecular Genetic Analysis of Populations. Second Edition. Practical Approach Series. Edited by A. R. HOELZEL. Oxford, New York, Tokyo: IRL Press at Oxford University Press. 1998. Pp. xxii+445. £29.95 (paperback).
DOI: 10.1017/S0003480099217538(Journal) (7037148-N)
DOI: 10.1046/j.1469-1809.1999.63302731.x(Journal)
==========================================================

Created: 2023-11-20 07:22:29
ConfID: 7037143
CauseID: 1597935851
OtherID: 5356
JT: Annals of Human Genetics
MD: AULCHENKO,63,4,351,1999,An example of complex segregation analysis of plant pedigree: reversion of cytoplasm type in Sugar Beet (Beta vulgaris L.)
DOI: 10.1017/S0003480099227625(Journal) (7037143-N)
DOI: 10.1111/j.1469-1809.1999.ahg634_0351_2.x(Journal)
==========================================================

Created: 2023-11-20 07:22:30
ConfID: 7037142
CauseID: 1597935855
OtherID: 5360
JT: Annals of Human Genetics
MD: HUMPHRIES,63,4,377,1999,Evolutionary Aspects of Nutrition and Health: Diet, Exercise, Genetics and Chronic Disease. World Review of Nutrition and Dietetics, vol. 84. Edited by A. P. SIMOPOULOS. Basel: Karger. 1999. Pp. 145. US $172.25, Sw.Fr. 198, DM 237.
DOI: 10.1017/S0003480099217642(Journal) (7037142-N)
DOI: 10.1046/j.1469-1809.1999.63403771.x(Journal)
==========================================================

Created: 2023-11-20 07:00:47
ConfID: 7037067
CauseID: 1597930996
OtherID: 5355
JT: Annals of Human Genetics
MD: PETRONZELLI,61,4,307,1997,Genetic contribution of the HLA region to the familial clustering of coeliac disease
DOI: 10.1017/S0003480097006258(Journal) (7037067-N)
DOI: 10.1046/j.1469-1809.1997.6140307.x(Journal)
==========================================================

Created: 2023-11-20 07:00:47
ConfID: 7037066
CauseID: 1597930996
OtherID: 5355
JT: Annals of Human Genetics
MD: FERNIE,61,4,287,1997,DNA haplotypes of the complement C6 and C7 genes associated with deficiencies of the seventh component; and a new DNA polymorphism in C7 exon 13
DOI: 10.1017/S0003480097006234(Journal) (7037066-N)
DOI: 10.1046/j.1469-1809.1997.6140287.x(Journal)
==========================================================

Created: 2023-11-20 07:00:47
ConfID: 7037065
CauseID: 1597930996
OtherID: 5355
JT: Annals of Human Genetics
MD: HUMPHREY,61,4,299,1997,Cloning and evaluation of RALGDS as a candidate for the tuberous sclerosis gene TSC1
DOI: 10.1017/S0003480097006246(Journal) (7037065-N)
DOI: 10.1046/j.1469-1809.1997.6140299.x(Journal)
==========================================================

Created: 2023-11-20 07:00:47
ConfID: 7037064
CauseID: 1597930996
OtherID: 5355
JT: Annals of Human Genetics
MD: BRETT,61,4,383,1997,In the Blood: God, Genes and Destiny. (Book of the major BBC television series.) By Steve Jones. London: HarperCollins. 1996. Pp. 302. £20.00.
DOI: 10.1017/S0003480097006337(Journal) (7037064-N)
DOI: 10.1046/j.1469-1809.1997.6140383.x(Journal)
==========================================================

Created: 2023-11-20 07:00:54
ConfID: 7037071
CauseID: 1597931035
OtherID: 5355
JT: Annals of Human Genetics
MD: TAYLOR,61,3,283,1997,Human Molecular Genetics. By T. Strachan and A. P. Read. Oxford: Bios Scientific Publishers. 1996. ISBN 1 872748 69 4. Pp. 596 + Index. £29.95.
DOI: 10.1017/S0003480097216222(Journal) (7037071-N)
DOI: 10.1046/j.1469-1809.1997.61302831.x(Journal)
==========================================================

Created: 2023-11-20 07:00:49
ConfID: 7037070
CauseID: 1597931002
OtherID: 5355
JT: Annals of Human Genetics
MD: ADLER,61,2,173,1997,Environmental Mutagenesis. Edited by D. H. Phillips and S. Venitt, Bios Scientific Publishers, Oxford, U.K., 1995, Pp. 403.
DOI: 10.1017/S0003480097216076(Journal) (7037070-N)
DOI: 10.1046/j.1469-1809.1997.61201731.x(Journal)
==========================================================

Created: 2023-11-20 07:00:47
ConfID: 7037069
CauseID: 1597930996
OtherID: 5355
JT: Annals of Human Genetics
MD: VON SCHNAKENBURG,61,4,365,1997,Linkage of microsatellites to the AGXT gene on chromosome 2q37.3 and their role in prenatal diagnosis of primary hyperoxaluria type 1
DOI: 10.1017/S0003480097006283(Journal) (7037069-N)
DOI: 10.1046/j.1469-1809.1997.6140365.x(Journal)
==========================================================

Created: 2023-11-20 07:00:47
ConfID: 7037068
CauseID: 1597930996
OtherID: 5355
JT: Annals of Human Genetics
MD: TOWNSEND,61,4,375,1997,Assignment of the human cardiac/slow skeletal muscle troponin C gene (TNNC1) between D3S3118 and GCT4B10 on the short arm of chromosome 3 by somatic cell hybrid analysis
DOI: 10.1017/S0003480097006301(Journal) (7037068-N)
DOI: 10.1046/j.1469-1809.1997.6140375.x(Journal)
==========================================================

Created: 2023-11-20 07:00:27
ConfID: 7037059
CauseID: 1597930941
OtherID: 5355
JT: Annals of Human Genetics
MD: MOURRIERAS,61,1,35,1997,Assessment of genetic diversity in space by superimposition of a distorted geographic map with a spatial population clustering. Application to GM haplotypes of native Amerindian tribes
DOI: 10.1017/S000348009600591X(Journal) (7037059-N)
DOI: 10.1046/j.1469-1809.1997.6110035.x(Journal)
==========================================================

Created: 2023-11-20 07:00:27
ConfID: 7037058
CauseID: 1597930941
OtherID: 5355
JT: Annals of Human Genetics
MD: ZAPATA,61,1,69,1997,On Fisher's exact test for detecting gametic disequilibrium between DNA polymorphisms
DOI: 10.1017/S0003480096005969(Journal) (7037058-N)
DOI: 10.1046/j.1469-1809.1997.6110069.x(Journal)
==========================================================

Created: 2023-11-20 07:00:25
ConfID: 7037057
CauseID: 1597930934
OtherID: 33686200
JT: Annals of Human Genetics
MD: MARTINELLI,65,5,465,2001,Linkage analysis of three candidate regions of chromosome 1 in nonsyndromic familial orofacial cleft
DOI: 10.1046/j.1469-1809.2001.6550465.x(Journal) (7037057-N)
DOI: 10.1017/S000348000100882X(Journal)
==========================================================

Created: 2023-11-20 07:00:27
ConfID: 7037063
CauseID: 1597930941
OtherID: 5355
JT: Annals of Human Genetics
MD: MORTON,61,1,1,1997,Genetic Epidemiology
DOI: 10.1017/S0003480096005891(Journal) (7037063-N)
DOI: 10.1046/j.1469-1809.1997.6110001.x(Journal)
==========================================================

Created: 2023-11-20 07:00:27
ConfID: 7037062
CauseID: 1597930941
OtherID: 5355
JT: Annals of Human Genetics
MD: STILL,61,1,15,1997,Fine structure physical mapping of a 1·9 Mb region of chromosome 13q12
DOI: 10.1017/S0003480096005908(Journal) (7037062-N)
DOI: 10.1046/j.1469-1809.1997.6140379.x(Journal)
==========================================================

Created: 2023-11-20 07:00:27
ConfID: 7037061
CauseID: 1597930941
OtherID: 5355
JT: Annals of Human Genetics
MD: GÉNIN,61,1,25,1997,Information provided by pairs of distantly affected relatives to search for genes involved in rare autosomal dominant diseases
DOI: 10.1017/S0003480096005970(Journal) (7037061-N)
DOI: 10.1046/j.1469-1809.1997.6110025.x(Journal)
==========================================================

Created: 2023-11-20 07:00:25
ConfID: 7037060
CauseID: 1597930934
OtherID: 33686200
JT: Annals of Human Genetics
MD: ENNIS,65,5,503,2001,Allelic association discriminates draft orders
DOI: 10.1046/j.1469-1809.2001.6550503.x(Journal) (7037060-N)
DOI: 10.1017/S000348000100879X(Journal)
==========================================================

Created: 2023-11-20 07:00:58
ConfID: 7037075
CauseID: 1597931053
OtherID: 5355
JT: Annals of Human Genetics
MD: WOLFE,61,5,401,1997,Mapping ESTs to the TSC1 candidate interval by use of the ‘Science 96’ transcript map
DOI: 10.1017/S0003480097006350(Journal) (7037075-N)
DOI: 10.1046/j.1469-1809.1997.6150401.x(Journal)
==========================================================

Created: 2023-11-20 07:00:54
ConfID: 7037074
CauseID: 1597931035
OtherID: 5355
JT: Annals of Human Genetics
MD: STOESZ,61,3,263,1997,Extension of the Haseman–Elston method to multiple alleles and multiple loci: theory and practice for candidate genes
DOI: 10.1017/S0003480097006179(Journal) (7037074-N)
DOI: 10.1046/j.1469-1809.1997.6130263.x(Journal)
==========================================================

Created: 2023-11-20 07:00:54
ConfID: 7037073
CauseID: 1597931035
OtherID: 5360
JT: Annals of Human Genetics
MD: POVEY,61,3,183,1997,REPORT on the Fifth International Workshop on Chromosome 9 held at Eynsham, Oxfordshire, UK, September 4–6, 1996
DOI: 10.1017/S0003480097006106(Journal) (7037073-N)
DOI: 10.1046/j.1469-1809.1997.6130183.x(Journal)
==========================================================

Created: 2023-11-20 07:00:54
ConfID: 7037072
CauseID: 1597931035
OtherID: 5355
JT: Annals of Human Genetics
MD: TSUKAMOTO,61,3,235,1997,Mutations associated with Sjögren–Larsson Syndrome
DOI: 10.1017/S0003480097006143(Journal) (7037072-N)
DOI: 10.1046/j.1469-1809.1997.6130235.x(Journal)
==========================================================

Created: 2023-11-20 07:02:01
ConfID: 7037078
CauseID: 1597931290
OtherID: 5349
JT: Annals of Human Genetics
MD: LE HELLARD,65,3,221,2001,Physical mapping: integrating computational and molecular genetic data
DOI: 10.1017/S0003480001008594(Journal) (7037078-N)
DOI: 10.1046/j.1469-1809.2001.6530221.x(Journal)
==========================================================

Created: 2023-11-20 07:01:11
ConfID: 7037077
CauseID: 1597931109
OtherID: 5355
JT: Annals of Human Genetics
MD: ,61,6,531,1997,European Mathematical Genetics Meeting held at Munich, 5–7 April 1997
DOI: 10.1017/S000348009700657X(Journal) (7037077-N)
DOI: 10.1046/j.1469-1809.1997.6160531.x(Journal)
==========================================================

Created: 2023-11-20 07:00:58
ConfID: 7037076
CauseID: 1597931053
OtherID: 5355
JT: Annals of Human Genetics
MD: DRUMMOND,61,5,393,1997,Cloning and chromosome assignment of the human CDX2 gene
DOI: 10.1017/S0003480097006465(Journal) (7037076-N)
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