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2. A Novel Mutation of Unal E; Yıldırım R; Tekin S; Demir V; Onay H; Haspolat YK J Clin Res Pediatr Endocrinol; 2018 Nov; 10(4):387-390. PubMed ID: 29687786 [TBL] [Abstract][Full Text] [Related]
3. A novel mutation of anti-Mullerian hormone gene in Persistent Mullerian Duct Syndrome presented with bilateral cryptorchidism: a case report. Wongprasert H; Somanunt S; De Filippo R; Picard JY; Pitukcheewanont P J Pediatr Urol; 2013 Aug; 9(4):e147-9. PubMed ID: 23611722 [TBL] [Abstract][Full Text] [Related]
4. Persistent Müllerian duct syndrome: A novel mutation in the Αnti-Müllerian Ηormone gene. Altincik A; Karaca F; Onay H Hormones (Athens); 2017 Apr; 16(2):205-208. PubMed ID: 28742509 [TBL] [Abstract][Full Text] [Related]
5. Novel AMH and AMHR2 Mutations in Two Egyptian Families with Persistent Müllerian Duct Syndrome. Mazen I; El-Gammal M; McElreavey K; Elaidy A; Abdel-Hamid MS Sex Dev; 2017; 11(1):29-33. PubMed ID: 28142151 [TBL] [Abstract][Full Text] [Related]
6. Clinical aspects and molecular genetics of persistent müllerian duct syndrome associated with transverse testicular ectopia: report of three cases. Ju X; Li Z; Zhang C; Qin C; Shao P; Li J; Li P; Cao Q; Zhang W; Wang Z; Yin C Urol Int; 2013; 90(1):83-6. PubMed ID: 23147169 [TBL] [Abstract][Full Text] [Related]
7. Persistent Müllerian Duct Syndrome Caused by a Novel Mutation of an Anti-MüIlerian Hormone Receptor Gene: Case Presentation and Literature Review. Elias-Assad G; Elias M; Kanety H; Pressman A; Tenenbaum-Rakover Y Pediatr Endocrinol Rev; 2016 Jun; 13(4):731-40. PubMed ID: 27464416 [TBL] [Abstract][Full Text] [Related]
8. A novel mutation of AMH in three siblings with persistent Mullerian duct syndrome. Nalbantoğlu Ö; Demir K; Korkmaz HA; Büyükinan M; Yıldız M; Tunç S; Özkan B J Pediatr Endocrinol Metab; 2015 Nov; 28(11-12):1379-82. PubMed ID: 26181047 [TBL] [Abstract][Full Text] [Related]
9. A Novel Mutation of AMHR2 In Two Siblings with Persistent Müllerian Duct Syndrome. Çakır AD; Turan H; Onay H; Emir H; Emre S; Comunoglu N; Ercan O; Evliyaoglu O Sex Dev; 2017; 11(5-6):289-292. PubMed ID: 29332065 [TBL] [Abstract][Full Text] [Related]
10. Persistent Müllerian duct syndrome: 8 new cases in Southern California and a review of the literature. Salehi P; Koh CJ; Pitukcheewanont P; Trinh L; Daniels M; Geffner M Pediatr Endocrinol Rev; 2012 Dec-2013 Jan; 10(2):227-33. PubMed ID: 23539834 [TBL] [Abstract][Full Text] [Related]
11. Two heterozygous mutations of the AMH gene in a Japanese patient with persistent Müllerian duct syndrome. Morikawa S; Moriya K; Ishizu K; Tajima T J Pediatr Endocrinol Metab; 2014 Nov; 27(11-12):1223-6. PubMed ID: 25026127 [TBL] [Abstract][Full Text] [Related]
14. Lack of causative mutation in the AMH and AMHR2 genes in a cat (38,XY) with persistent Mullerian duct syndrome (PMDS). Rozynek J; Nowacka-Woszuk J; Stachowiak M; Sowinska N; Lukomska A; Gruss M; Switonski M; Szczerbal I Reprod Domest Anim; 2024 Jun; 59(6):e14635. PubMed ID: 38837470 [TBL] [Abstract][Full Text] [Related]
15. [A rare cause of cryptorchidism, the persistence of müllerian ducts syndrome]. Lavergne O; Troisfontaines E; Verstraete A; Demarche M; Nicolas H Rev Med Liege; 2018 Jul; 73(7-8):376-379. PubMed ID: 30113777 [TBL] [Abstract][Full Text] [Related]
16. [Persistent Müllerian duct syndrome due to a mutation in the anti-Müllerian hormone receptor gene (AMHR2)]. Orós-Millán ME; Muñoz-Calvo MT; Nishi MY; Bilharinho Mendonca B; Argente J An Pediatr (Barc); 2017 Feb; 86(2):94-95. PubMed ID: 27461869 [No Abstract] [Full Text] [Related]
17. Persistent Mullerian duct syndrome with transverse testicular ectopia: rare presentation of inguinal hernia. Gupta A; Panda N; Saha ML; Ganguly S; Bandyopadhyay SK; Das R Urol J; 2013; 10(2):909-11. PubMed ID: 23801478 [No Abstract] [Full Text] [Related]
18. A novel mutation in the anti-müllerian hormone gene as cause of persistent müllerian duct syndrome. Lang-Muritano M; Biason-Lauber A; Gitzelmann C; Belville C; Picard Y; Schoenle EJ Eur J Pediatr; 2001 Nov; 160(11):652-4. PubMed ID: 11760020 [TBL] [Abstract][Full Text] [Related]
19. AMH gene mutations in two Egyptian families with persistent müllerian duct syndrome. Mazen I; Abdel Hamid MS; El-Gammal M; Aref A; Amr K Sex Dev; 2011; 5(6):277-80. PubMed ID: 22188863 [TBL] [Abstract][Full Text] [Related]
20. Identification of four novel variant in the AMHR2 gene in six unrelated Turkish families. Unal E; Karakaya AA; Beştaş A; Yıldırım R; Taş FF; Onay H; Özkınay F; Haspolat YK J Endocrinol Invest; 2021 Jun; 44(6):1301-1307. PubMed ID: 33025551 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]