Report date: Apr 30, 2024
Conflict count: 350192
Publisher: Ovid Technologies (Wolters Kluwer)  - Lippincott Williams & Wilkins
Title count: 161
Conflict count: 5838


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Created: 2021-01-21 22:04:06.0
ConfID: 5943140
CauseID: 1487150240
OtherID: 302884016
JT: Clinical Dysmorphology
MD: Neas, 12 ,3,179,2003,A case of partial trisomy 4p syndrome presenting as severe hydronephrosis in utero
DOI: 10.1097/00019605-200307000-00006(Journal) (5943140-N )
DOI: 10.1097/01.mcd.0000072162.33788.8d(Journal)
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Created: 2021-01-21 22:04:08.0
ConfID: 5943141
CauseID: 1487150242
OtherID: 302884016
JT: Clinical Dysmorphology
MD: Labrune, 12 ,3,213,2003,Absence of specific facial dysmorphy in glycogen storage disease type III
DOI: 10.1097/00019605-200307000-00017(Journal) (5943141-N )
DOI: 10.1097/01.mcd.0000052342.43310.35(Journal)
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Created: 2021-01-21 22:04:08.0
ConfID: 5943142
CauseID: 1487150243
OtherID: 302884016
JT: Clinical Dysmorphology
MD: Zackai, 12 ,3,209,2003,Craniosynostosis with tracheal sleeve: a patient with Pfeiffer syndrome, tracheal sleeve and additional malformations in whom an FGFR2 mutation was found
DOI: 10.1097/00019605-200307000-00015(Journal) (5943142-N )
DOI: 10.1097/01.mcd.0000080414.95344.ae(Journal)
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Created: 2021-01-21 22:04:08.0
ConfID: 5943143
CauseID: 1487150244
OtherID: 302884016
JT: Clinical Dysmorphology
MD: Talisetti, 12 ,3,175,2003,Temtamy-like syndrome associated with translocation of 2p24 and 9q32
DOI: 10.1097/00019605-200307000-00005(Journal) (5943143-N )
DOI: 10.1097/01.mcd.0000072161.33788.56(Journal)
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Created: 2021-01-21 22:04:08.0
ConfID: 5943144
CauseID: 1487150245
OtherID: 302884016
JT: Clinical Dysmorphology
MD: Zelante, 12 ,3,207,2003,Fusion of vertebrae, diaphragmatic hernia and unusual facies in a girl: a possible further case of Mathieu syndrome
DOI: 10.1097/00019605-200307000-00014(Journal) (5943144-N )
DOI: 10.1097/01.mcd.0000077562.66911.8d(Journal)
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Created: 2021-01-21 22:04:06.0
ConfID: 5943145
CauseID: 1487150250
OtherID: 302884016
JT: Clinical Dysmorphology
MD: Sanders, 12 ,3,183,2003,Interstitial deletion of chromosome 2p16.2p21
DOI: 10.1097/00019605-200307000-00007(Journal) (5943145-N )
DOI: 10.1097/01.mcd.0000065051.36236.e9(Journal)
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Created: 2021-01-21 22:04:07.0
ConfID: 5943146
CauseID: 1487150251
OtherID: 302884016
JT: Clinical Dysmorphology
MD: Slavotinek, 12 ,3,195,2003,Large interstitial deletion of chromosome 13q and severe short stature: clinical report and review of the literature
DOI: 10.1097/00019605-200307000-00010(Journal) (5943146-N )
DOI: 10.1097/01.mcd.0000072160.33788.1f(Journal)
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Created: 2021-01-21 22:04:09.0
ConfID: 5943147
CauseID: 1487150253
OtherID: 302884016
JT: Clinical Dysmorphology
MD: McGaughran, 12 ,3,197,2003,Klippel-Feil anomaly in Fanconi anemia
DOI: 10.1097/00019605-200307000-00011(Journal) (5943147-N )
DOI: 10.1097/01.mcd.0000077560.66911.1f(Journal)
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Created: 2021-01-21 22:04:06.0
ConfID: 5943148
CauseID: 1487150256
OtherID: 302884016
JT: Clinical Dysmorphology
MD: Koenig, 12 ,3,187,2003,Teebi hypertelorism syndrome
DOI: 10.1097/00019605-200307000-00008(Journal) (5943148-N )
DOI: 10.1097/01.mcd.0000077563.66911.c4(Journal)
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Created: 2021-01-21 22:04:10.0
ConfID: 5943149
CauseID: 1487150262
OtherID: 302884016
JT: Clinical Dysmorphology
MD: AlKaissi, 12 ,3,191,2003,Siblings with glaucoma, mental retardation and short stature
DOI: 10.1097/00019605-200307000-00009(Journal) (5943149-N )
DOI: 10.1097/01.mcd.0000077564.66911.0a(Journal)
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Created: 2021-01-21 22:04:11.0
ConfID: 5943150
CauseID: 1487150263
OtherID: 302884016
JT: Clinical Dysmorphology
MD: Kamoda, 12 ,3,211,2003,Osteofibrous dysplasia in a Japanese boy with Costello syndrome
DOI: 10.1097/00019605-200307000-00016(Journal) (5943150-N )
DOI: 10.1097/01.mcd.0000080412.95344.29(Journal)
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Created: 2021-01-21 22:04:10.0
ConfID: 5943151
CauseID: 1487150270
OtherID: 302884016
JT: Clinical Dysmorphology
MD: Al Attia, 12 ,3,203,2003,A patient with extensive blue rubber bleb nevi associated with multiple congenital anomalies: An overlap or a new syndrome?
DOI: 10.1097/00019605-200307000-00013(Journal) (5943151-N )
DOI: 10.1097/01.mcd.0000077561.66911.56(Journal)
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Created: 2021-01-21 22:04:10.0
ConfID: 5943152
CauseID: 1487150271
OtherID: 302884016
JT: Clinical Dysmorphology
MD: Morava, 12 ,3,161,2003,Ulnar/fibular ray defect and brachydactyly in a family: a possible new autosomal dominant syndrome
DOI: 10.1097/00019605-200307000-00002(Journal) (5943152-N )
DOI: 10.1097/01.mcd.0000072164.33788.0a(Journal)