Guerrier D - Search Results

1

Phenotypic variability of a 4q34-->qter inherited deletion: MRKH syndrome in the daughter, cardiac defect and Fallopian tube cancer in the mother.

Bendavid C, Pasquier L, Watrin T, Morcel K, Lucas J, Gicquel I, Dubourg C, Henry C, David V, Odent S, Levêque J, Pellerin I, Guerrier D. Bendavid C, et al. Among authors: guerrier d. Eur J Med Genet. 2007 Jan-Feb;50(1):66-72. doi: 10.1016/j.ejmg.2006.09.003. Epub 2006 Oct 1. Eur J Med Genet. 2007. PMID: 17081814

2

[The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: clinical description and genetics].

Morcel K, Guerrier D, Watrin T, Pellerin I, Levêque J. Morcel K, et al. Among authors: guerrier d. J Gynecol Obstet Biol Reprod (Paris). 2008 Oct;37(6):539-46. doi: 10.1016/j.jgyn.2008.07.002. Epub 2008 Aug 23. J Gynecol Obstet Biol Reprod (Paris). 2008. PMID: 18723299 Review. French.

3

The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina)--phenotypic manifestations and genetic approaches.

Guerrier D, Mouchel T, Pasquier L, Pellerin I. Guerrier D, et al. J Negat Results Biomed. 2006 Jan 27;5:1. doi: 10.1186/1477-5751-5-1. J Negat Results Biomed. 2006. PMID: 16441882 Free PMC article. Review.

4

Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina).

Burel A, Mouchel T, Odent S, Tiker F, Knebelmann B, Pellerin I, Guerrier D. Burel A, et al. Among authors: guerrier d. J Negat Results Biomed. 2006 Mar 23;5:4. doi: 10.1186/1477-5751-5-4. J Negat Results Biomed. 2006. PMID: 16556301 Free PMC article.

5

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome.

Morcel K, Camborieux L; Programme de Recherches sur les Aplasies Müllériennes; Guerrier D. Morcel K, et al. Among authors: guerrier d. Orphanet J Rare Dis. 2007 Mar 14;2:13. doi: 10.1186/1750-1172-2-13. Orphanet J Rare Dis. 2007. PMID: 17359527 Free PMC article. Review.

6

Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci.

Morcel K, Watrin T, Pasquier L, Rochard L, Le Caignec C, Dubourg C, Loget P, Paniel BJ, Odent S, David V, Pellerin I, Bendavid C, Guerrier D. Morcel K, et al. Among authors: guerrier d. Orphanet J Rare Dis. 2011 Mar 15;6:9. doi: 10.1186/1750-1172-6-9. Orphanet J Rare Dis. 2011. PMID: 21406098 Free PMC article.

7

Clinical utility gene card for: Mayer-Rokitansky-Küster-Hauser syndrome.

Morcel K, Dallapiccola B, Pasquier L, Watrin T, Bernardini L, Guerrier D. Morcel K, et al. Among authors: guerrier d. Eur J Hum Genet. 2012 Feb;20(2). doi: 10.1038/ejhg.2011.158. Epub 2011 Sep 7. Eur J Hum Genet. 2012. PMID: 21897448 Free PMC article. No abstract available.

8

GREB1L variants in familial and sporadic hereditary urogenital adysplasia and Mayer-Rokitansky-Kuster-Hauser syndrome.

Jacquinet A, Boujemla B, Fasquelle C, Thiry J, Josse C, Lumaka A, Brischoux-Boucher E, Dubourg C, David V, Pasquier L, Lehman A, Morcel K, Guerrier D, Bours V. Jacquinet A, et al. Among authors: guerrier d. Clin Genet. 2020 Aug;98(2):126-137. doi: 10.1111/cge.13769. Epub 2020 May 25. Clin Genet. 2020. PMID: 32378186 Free article.

9

Involvement of ITIH5, a candidate gene for congenital uterovaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome), in female genital tract development.

Morcel K, Watrin T, Jaffre F, Deschamps S, Omilli F, Pellerin I, Levêque J, Guerrier D. Morcel K, et al. Among authors: guerrier d. Gene Expr. 2012;15(5-6):207-14. doi: 10.3727/105221613x13571653093169. Gene Expr. 2012. PMID: 23539898 Free PMC article.

10

The developing female genital tract: from genetics to epigenetics.

Massé J, Watrin T, Laurent A, Deschamps S, Guerrier D, Pellerin I. Massé J, et al. Among authors: guerrier d. Int J Dev Biol. 2009;53(2-3):411-24. doi: 10.1387/ijdb.082680jm. Int J Dev Biol. 2009. PMID: 19412895 Free article. Review.

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