Toutain A - Search Results

1

Möbius sequence, Robin complex, and hypotonia: severe expression of brainstem disruption spectrum versus Carey-Fineman-Ziter syndrome.

Verloes A, Bitoun P, Heuskin A, Amrom D, van de Broeck H, Nikkel SM, Chudley AE, Prasad AN, Rusu C, Covic M, Toutain A, Moraine C, Parisi MA, Patton M, Martin JJ, Van Thienen MN. Verloes A, et al. Among authors: toutain a. Am J Med Genet A. 2004 Jun 15;127A(3):277-87. doi: 10.1002/ajmg.a.20687. Am J Med Genet A. 2004. PMID: 15150779

2

Monosomy 6q: report on four new cases.

Valtat C, Galliano D, Mettey R, Toutain A, Moraine C. Valtat C, et al. Among authors: toutain a. Clin Genet. 1992 Mar;41(3):159-66. doi: 10.1111/j.1399-0004.1992.tb03655.x. Clin Genet. 1992. PMID: 1563091 Review.

3

Lumping Juberg-Marsidi syndrome and X-linked alpha-thalassemia/mental retardation syndrome?

Saugier-Veber P, Munnich A, Lyonnet S, Toutain A, Moraine C, Piussan C, Mathieu M, Gibbons RJ. Saugier-Veber P, et al. Among authors: toutain a. Am J Med Genet. 1995 Jan 30;55(3):300-1. doi: 10.1002/ajmg.1320550310. Am J Med Genet. 1995. PMID: 7726226 No abstract available.

4

X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome. Report of three male patients in a large French family.

Lefort G, Taib J, Toutain A, Houdayer C, Moraine CI, Humeau C, Sarda P. Lefort G, et al. Among authors: toutain a. Ann Genet. 1993;36(4):200-5. Ann Genet. 1993. PMID: 8166424

5

Splicing mutation in the ATR-X gene can lead to a dysmorphic mental retardation phenotype without alpha-thalassemia.

Villard L, Toutain A, Lossi AM, Gecz J, Houdayer C, Moraine C, Fontès M. Villard L, et al. Among authors: toutain a. Am J Hum Genet. 1996 Mar;58(3):499-505. Am J Hum Genet. 1996. PMID: 8644709 Free PMC article.

6

X-linked mental retardation with neonatal hypotonia in a French family (MRX15): gene assignment to Xp11.22-Xp21.1.

Raynaud M, Gendrot C, Dessay B, Moncla A, Ayrault AD, Moizard MP, Toutain A, Briault S, Villard L, Ronce N, Moraine C. Raynaud M, et al. Among authors: toutain a. Am J Med Genet. 1996 Jul 12;64(1):97-106. doi: 10.1002/(SICI)1096-8628(19960712)64:1<97::AID-AJMG17>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8826458

7

Opitz GBBB syndrome: chromosomal evidence of an X-linked form.

Verloes A, David A, Odent S, Toutain A, André MJ, Lucas J, Le Marec B. Verloes A, et al. Among authors: toutain a. Am J Med Genet. 1995 Oct 23;59(1):123-8. doi: 10.1002/ajmg.1320590124. Am J Med Genet. 1995. PMID: 8849003

8

Nance-Horan syndrome: linkage analysis in 4 families refines localization in Xp22.31-p22.13 region.

Toutain A, Ronce N, Dessay B, Robb L, Francannet C, Le Merrer M, Briard ML, Kaplan J, Moraine C. Toutain A, et al. Hum Genet. 1997 Feb;99(2):256-61. doi: 10.1007/s004390050349. Hum Genet. 1997. PMID: 9048931

9

Deafness and Mondini dysplasia in Kabuki (Niikawa-Kuroki) syndrome. Report of a case and review of the literature.

Toutain A, Plée Y, Ployet MJ, Benoit S, Perrot A, Sembely C, Barthez MA, Moraine C. Toutain A, et al. Genet Couns. 1997;8(2):99-105. Genet Couns. 1997. PMID: 9219007 Review.

10

Mental retardation in Nance-Horan syndrome: clinical and neuropsychological assessment in four families.

Toutain A, Ayrault AD, Moraine C. Toutain A, et al. Am J Med Genet. 1997 Aug 22;71(3):305-14. doi: 10.1002/(sici)1096-8628(19970822)71:3<305::aid-ajmg11>3.0.co;2-o. Am J Med Genet. 1997. PMID: 9268101 Review.

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