Results 91 to 100 of about 68,843 (129)

A de novo SOX11 mutation causing hypogonadotropic hypogonadism: a case report and literature review. [PDF]

BMC Pediatr
Chu S, Yuan X, Niu Q, Gu W.
europepmc   +1 more source

A highly rare female phenotype with complex chromosomal mosaicism: 46,XY/45,X/46,X,r(Y). [PDF]

Clin Exp Reprod Med
Maghsoomi Z, Abiri M, Golgiri F, Iraji H, Ghahestani SM, Tajikrostami F, Emtiazi N, Eghbali M.   +7 more
europepmc   +1 more source

Ovotesticular disorder of sex development presenting in adolescence with amenorrhea and clitoromegaly-what is your diagnosis? [PDF]

J Turk Ger Gynecol Assoc
Setty A, Mangla M, Reddy KKK, Velladurai M.   +3 more
europepmc   +1 more source

Case Report: Compound heterozygous mutations in the <i>IDUA</i> gene causing mucopolysaccharidosis type I with uterine developmental abnormality. [PDF]

Front Pediatr
Xu Y, Li J, Wang L, Pan S, Fan Y.
europepmc   +1 more source

Evaluation of the incidence of congenital uterine anomalies in polycystic ovarian syndrome: tertiary center experience. [PDF]

Front Med (Lausanne)
Yavuz O, Akdöner A, Mankan KA, Gündoğan K, Okyay RE, Doğan ÖE.   +5 more
europepmc   +1 more source

Comparison of Different Classification Systems for Müllerian Duct Anomalies: A Retrospective Observational MRI Study. [PDF]

Medicina (Kaunas)
D'hoore L, Decroos E, De Visschere PJL, Battaglia O, Hamerlynck T.   +4 more
europepmc   +1 more source

A case report on atypical chromosomal variations in Turner syndrome. [PDF]

Mol Cytogenet
Aliazami F, Farhud DD, Zarif-Yeganeh M, Shahmoradi SS, Tajik B, Jaryani S.   +5 more
europepmc   +1 more source

Pregnancy Complications in Uterine Anomalies-A Pilot Study. [PDF]

J Clin Med
Voic C, Mitranovici MI, Voidazan S, Mureşan CM, Bernad ES.   +4 more
europepmc   +1 more source

Report of the favorable pregnancy outcomes in an FKBP10-related Bruck syndrome case and a narrative review of pregnancy in severe osteogenesis imperfecta. [PDF]

BMC Pregnancy Childbirth
Sriudomporn K, Sura T, Tunteeratum A, Tangshewinsirikul C, Lertrat W, Diawtipsukon S.   +5 more
europepmc   +1 more source

Rare Endocrine Disorders in Children of Consanguineous Parents: A Case Series. [PDF]

Cureus
Khaled Ali Abdulla AlKhalifa H, AlQanea F, Flood J.   +2 more
europepmc   +1 more source