PubMed for id: 1657403

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Year	Number of Results
1993	1
2009	1
2019	1
2024	0

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Whole-exome sequencing identifies a GREB1L variant in a three-generation family with Müllerian and renal agenesis: a novel candidate gene in Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome. A case report.

Herlin MK, Le VQ, Højland AT, Ernst A, Okkels H, Petersen AC, Petersen MB, Pedersen IS. Herlin MK, et al. Hum Reprod. 2019 Sep 29;34(9):1838-1846. doi: 10.1093/humrep/dez126. Hum Reprod. 2019. PMID: 31424080

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. Bernardini L, et al. Orphanet J Rare Dis. 2009 Nov 4;4:25. doi: 10.1186/1750-1172-4-25. Orphanet J Rare Dis. 2009. PMID: 19889212 Free PMC article.

Familial occurrence of hereditary renal adysplasia with müllerian anomalies.

Battin J, Lacombe D, Leng JJ. Battin J, et al. Clin Genet. 1993 Jan;43(1):23-4. doi: 10.1111/j.1399-0004.1993.tb04420.x. Clin Genet. 1993. PMID: 8462192

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