Mayer-Rokitansky-Kuster-Hauser Syndrome US Aid To Diagnosis Abstract. The MayerRokitansky-Kuster-Hauser syndrome is composed of vaginal atresia with other variable M llerian duct abnormalities such as bicornuate or http://radiology.rsna.org/content/161/3/815.abstract
Mayer-Rokitansky-Kuster-Hauser Syndrome - Definition MayerRokitansky-Kuster-Hauser syndrome definition from the mondofacto online medical dictionary http://www.mondofacto.com/facts/dictionary?Mayer-Rokitansky-Kuster-Hauser syndro
WNT4 Deficiencya Clinical Phenotype Distinct From The Classic WNT4 deficiency—a clinical phenotype distinct from the classic Mayer–Rokitansky–Kuster–Hauser syndrome A Case Report A. BiasonLauber 1,3, G. De Filippo 2, D. Konrad 1, G http://humrep.oxfordjournals.org/cgi/content/full/22/1/224
Human Disease And Mouse Model Detail Human Disease Term MayerRokitansky-Kuster-Hauser Syndrome OMIM ID 277000. Synonyms Congenital Absence of Uterus and Vagina; CAUV; Mrk Anomaly; Mrkh Anomaly; Mrkh Syndrome; Mullerian http://www.informatics.jax.org/javawi2/servlet/WIFetch?page=humanDisease&key
Mayer-Rokitansky-Kuster-Hauser Syndrome Sexuality, Psychological Authors E. J. Bean, T. Mazur, A. D. Robinson. Citations 0 MayerRokitansky-Kuster-Hauser (MRKH) syn- drome is a congenital condition in which a genetic female is born with http://academic.research.microsoft.com/Paper/13892551.aspx
