Journal of Negative Results in BioMedicine | Articles which cite: Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina).

printer friendly

to [Help]

BioMed Central articles that cite the above article:

Research

Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports
Bernardini L, Gimelli S, Gervasini C, Carella M, Baban A, Frontino G, Barbano G, Divizia MT, Fedele L, Novelli A, Béna F, Lalatta F, Miozzo M, Dallapiccola B
Orphanet Journal of Rare Diseases 2009, 4:25 (4 November 2009)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles]

Review

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome
Morcel K, Camborieux L, Programme de Recherches sur les Aplasies Müllériennes (PRAM) , Guerrier D
Orphanet Journal of Rare Diseases 2007, 2:13 (14 March 2007)
[Abstract] [Full Text] [PDF] [PubMed] [Related articles] [Cited on BioMed Central]

This article is also cited by a further 1 article in PubMed Central

printer friendly

to [Help]