David A - Search Results

1

Vincent C, Mercier JM, David A. Vincent C, et al. Among authors: david a. Rev Stomatol Chir Maxillofac. 2008 Feb;109(1):44-7. doi: 10.1016/j.stomax.2007.10.005. Epub 2007 Dec 27. Rev Stomatol Chir Maxillofac. 2008. PMID: 18164045 French.

2

Child with manifestations of Nager acrofacial dysostosis, and the MURCS, VACTERL, and pulmonary agenesis associations: complex defect of blastogenesis?

David A, Mercier J, Verloes A. David A, et al. Am J Med Genet. 1996 Mar 1;62(1):1-5. doi: 10.1002/(SICI)1096-8628(19960301)62:1<1::AID-AJMG1>3.0.CO;2-1. Am J Med Genet. 1996. PMID: 8779315

3

[The genetics of labio-palatal clefts].

Rival JM, David A. Rival JM, et al. Among authors: david a. Rev Stomatol Chir Maxillofac. 2001 Jun;102(3-4):171-81. Rev Stomatol Chir Maxillofac. 2001. PMID: 11577471 Review. French.

4

Nosology of fetal hypokinesia sequence based on CNS abnormalities: is there an Aase-Smith syndrome?

David A, Nombalais MF, Rival JM, Verloes A. David A, et al. Clin Genet. 1996 Oct;50(4):251-4. doi: 10.1111/j.1399-0004.1996.tb02638.x. Clin Genet. 1996. PMID: 9001811

5

[Conradi-Hünermann-Happle syndrome with unilateral distribution].

Hello M, David A, Barbarot S. Hello M, et al. Among authors: david a. Ann Dermatol Venereol. 2010 Jan;137(1):44-7. doi: 10.1016/j.annder.2009.11.006. Epub 2009 Dec 29. Ann Dermatol Venereol. 2010. PMID: 20110068 French.

6

Autosomal dominant spondylocarpotarsal synostosis syndrome: phenotypic homogeneity and genetic heterogeneity.

Isidor B, Cormier-Daire V, Le Merrer M, Lefrancois T, Hamel A, Le Caignec C, David A, Jacquemont S. Isidor B, et al. Among authors: david a. Am J Med Genet A. 2008 Jun 15;146A(12):1593-7. doi: 10.1002/ajmg.a.32217. Am J Med Genet A. 2008. PMID: 18470895

7

[Otopalatodigital syndrome. Apropos of 3 female cases].

Plenier V, Delaire J, David A, Cohen JY. Plenier V, et al. Among authors: david a. Rev Stomatol Chir Maxillofac. 1983;84(6):322-9. Rev Stomatol Chir Maxillofac. 1983. PMID: 6583818 French.

8

[CLOVES syndrome: a malformational syndrome closely resembling Proteus syndrome].

Guillet A, Aubert H, Tessier MH, David A, Perret C, Penhoat M, Stalder JF, Barbarot S. Guillet A, et al. Among authors: david a. Ann Dermatol Venereol. 2014 Aug-Sep;141(8-9):507-13. doi: 10.1016/j.annder.2014.04.119. Epub 2014 Jun 2. Ann Dermatol Venereol. 2014. PMID: 25209813 French.

9

Currarino syndrome as an etiology of a neonatal Escherichia coli meningitis.

Fleury J, Picherot G, Cretolle C, Podevin G, David A, Caillon J, Roze JC, Gras-le Guen C. Fleury J, et al. Among authors: david a. J Perinatol. 2007 Sep;27(9):589-91. doi: 10.1038/sj.jp.7211783. J Perinatol. 2007. PMID: 17724455

10

Rubinstein-Taybi syndrome and Hirschsprung disease in a patient harboring an intragenic deletion of the CREBBP gene.

Isidor B, Podevin G, Camby C, Mosnier JF, Chauty A, Lyet JM, Fergelot P, Lacombe D, Arveiler B, Pelet A, Amiel J, David A. Isidor B, et al. Among authors: david a. Am J Med Genet A. 2010 Jul;152A(7):1847-8. doi: 10.1002/ajmg.a.33480. Am J Med Genet A. 2010. PMID: 20583168 Free article. No abstract available.

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