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Page 1
Orofaciodigital syndrome with cerebral dysgenesis.
Lesca G, Fallet-Bianco C, Plauchu H, Vitrey D, Verloes A, Attia-Sobol J. Lesca G, et al. Among authors: attia sobol j. Am J Med Genet A. 2006 Apr 1;140(7):757-63. doi: 10.1002/ajmg.a.31144. Am J Med Genet A. 2006. PMID: 16502430
Cerebral dysgenesis does not exclude OFD I syndrome.
Thauvin-Robinet C, Lesca G, Aral B, Gigot N, Lambert S, Gueneau L, Macca M, Franco B, Huet F, Zabot MT, Attié-Bitach T, Attia-Sobol J, Faivre L. Thauvin-Robinet C, et al. Among authors: attia sobol j. Am J Med Genet A. 2011 Feb;155A(2):455-7. doi: 10.1002/ajmg.a.33812. Epub 2011 Jan 13. Am J Med Genet A. 2011. PMID: 21271673 No abstract available.
Clinical and genetic heterogeneity of Seckel syndrome.
Faivre L, Le Merrer M, Lyonnet S, Plauchu H, Dagoneau N, Campos-Xavier AB, Attia-Sobol J, Verloes A, Munnich A, Cormier-Daire V. Faivre L, et al. Among authors: attia sobol j. Am J Med Genet. 2002 Nov 1;112(4):379-83. doi: 10.1002/ajmg.10677. Am J Med Genet. 2002. PMID: 12376940
Ectodermal abnormalities associated with methimazole intrauterine exposure.
Martin-Denavit T, Edery P, Plauchu H, Attia-Sobol J, Raudrant D, Aurand JM, Thomas L. Martin-Denavit T, et al. Am J Med Genet. 2000 Oct 2;94(4):338-40. doi: 10.1002/1096-8628(20001002)94:4<338::aid-ajmg13>3.0.co;2-6. Am J Med Genet. 2000. PMID: 11038449 No abstract available.
The spectrum of type III lissencephaly: a clinicopathological update.
Allias F, Buenerd A, Bouvier R, Attia-Sobol J, Dijoud F, Clémenson A, Encha-Razavi F. Allias F, et al. Among authors: attia sobol j. Fetal Pediatr Pathol. 2004 Sep-Dec;23(5-6):305-17. doi: 10.1080/15227950490952488. Fetal Pediatr Pathol. 2004. PMID: 16137167
14 results