Moraine C - Search Results

1

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

2

Structural rearrangements of chromosome 13 as additional abnormalities in Burkitt lymphoma and type 3 acute lymphoblastic leukemia.

Barin C, Valtat C, Briault S, Bremond JL, Petit A, Lejars O, Linassier C, Gaschard P, Moraine C. Barin C, et al. Among authors: moraine c. Cancer Genet Cytogenet. 1992 Jun;60(2):206-9. doi: 10.1016/0165-4608(92)90021-y. Cancer Genet Cytogenet. 1992. PMID: 1606568

3

X-linked mental retardation exhibiting linkage to DXS255 and PGKP1: a new MRX family (MRX14) with localization in the pericentromeric region.

Gendrot C, Ronce N, Toutain A, Moizard MP, Müh JP, Raynaud M, Dourlens J, Briault S, Moraine C. Gendrot C, et al. Among authors: moraine c. Clin Genet. 1994 Mar;45(3):145-53. doi: 10.1111/j.1399-0004.1994.tb04012.x. Clin Genet. 1994. PMID: 8026106

4

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. Among authors: moraine c. Hum Genet. 1997 Feb;99(2):256-61. doi: 10.1007/s004390050349. Hum Genet. 1997. PMID: 9048931

5

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

Toutain A, Ayrault AD, Moraine C. Toutain A, et al. Among authors: moraine c. 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.

6

Splenogonadal fusion limb defect syndrome: report of five new cases and review.

Bonneau D, Roume J, Gonzalez M, Toutain A, Carles D, Maréchaud M, Biran-Mucignat V, Amati P, Moraine C. Bonneau D, et al. Among authors: moraine c. Am J Med Genet. 1999 Oct 8;86(4):347-58. doi: 10.1002/(sici)1096-8628(19991008)86:4<347::aid-ajmg9>3.0.co;2-a. Am J Med Genet. 1999. PMID: 10494091 Review.

7

Twenty-five novel mutations including duplications in the ATP7A gene.

Moizard MP, Ronce N, Blesson S, Bieth E, Burglen L, Mignot C, Mortemousque I, Marmin N, Dessay B, Danesino C, Feillet F, Castelnau P, Toutain A, Moraine C, Raynaud M. Moizard MP, et al. Among authors: moraine c. Clin Genet. 2011 Mar;79(3):243-53. doi: 10.1111/j.1399-0004.2010.01461.x. Clin Genet. 2011. PMID: 21208200

8

Refinement of the NHS locus on chromosome Xp22.13 and analysis of five candidate genes.

Toutain A, Dessay B, Ronce N, Ferrante MI, Tranchemontagne J, Newbury-Ecob R, Wallgren-Pettersson C, Burn J, Kaplan J, Rossi A, Russo S, Walpole I, Hartsfield JK, Oyen N, Nemeth A, Bitoun P, Trump D, Moraine C, Franco B. Toutain A, et al. Among authors: moraine c. Eur J Hum Genet. 2002 Sep;10(9):516-20. doi: 10.1038/sj.ejhg.5200846. Eur J Hum Genet. 2002. PMID: 12173028

9

[Value of ultrasonic diagnosis of fetal malformations in the detection of chromosomal abnormalities].

Galliano D, Paillet C, Body G, Pierre F, Pourcelot D, Moraine C. Galliano D, et al. Among authors: moraine c. J Gynecol Obstet Biol Reprod (Paris). 1991;20(2):203-8. J Gynecol Obstet Biol Reprod (Paris). 1991. PMID: 2071864 French.

10

Prenatal diagnosis of trisomy 8 mosaicism in CVS after abnormal ultrasound findings at 12 weeks.

Guichet A, Briault S, Toutain A, Paillet C, Descamps P, Pierre F, Body G, Moraine C. Guichet A, et al. Among authors: moraine c. Prenat Diagn. 1995 Aug;15(8):769-72. doi: 10.1002/pd.1970150815. Prenat Diagn. 1995. PMID: 7479598

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