Results 121 to 130 of about 16,503 (187)

Molecular Genetics of Primary Congenital Hypothyroidism: Established and Emerging Contributors to Thyroid Dysgenesis. [PDF]

Int J Mol Sci
Dermitzaki N, Serbis A, Baltogianni M, Gialamprinou D, Giaprou LE, Kosmeri C, Giapros V.   +6 more
europepmc   +1 more source

A Case Report of a Syndromic Triad of Persistent Urogenital Sinus, Herlyn-Werner-Wunderlich Syndrome, and Prune Belly Syndrome in a Neonate. [PDF]

European J Pediatr Surg Rep
Grömping E, Hagens J, Schmidt HC, Wenke K, Tomuschat C, Reinshagen K.   +5 more
europepmc   +1 more source

XXX/XY chimerism with urogenital malformations in a Japanese black calf. [PDF]

Ir Vet J
Kanno C, Sugiyama M, Miura H, Ozawa S, Sato S, Kudo C, Kawaguchi H.   +6 more
europepmc   +1 more source

<i>PPP1R12A</i> mutation leads to different genders of twinning: a case report and literature review. [PDF]

Transl Pediatr
Tian H, Wu D, Yang H, Wu D, Tao C, Wei J, Yuan J, Fu J, Tang D, Yan X.   +9 more
europepmc   +1 more source

Prenatal Diagnosis of Fraser Syndrome at 20 Weeks' Gestation: A Case Report and Review of Literature. [PDF]

Cureus
Rana S.
europepmc   +1 more source

A novel 'wrap-and-patch' omental flap technique for the repair of uretero-uterine fistula: A case report. [PDF]

Urol Case Rep
Khalifa Salem MSE, Mukendi AM, Cele-Mbuthweni Z.   +2 more
europepmc   +1 more source

Vaginal septum in women: A review of diagnosis, management, and obstetric outcomes. [PDF]

Tzu Chi Med J
Wu YC, Li PC, Ding DC.
europepmc   +1 more source

A rare Zinner syndrome combined with testicular cancer: a case report. [PDF]

Front Oncol
Meng L, Shao Y, Jia Y, Deng X, Tang Y, Hu X, Wu K, Li X.   +7 more
europepmc   +1 more source

Incidental findings of ipsilateral agenesis of the ovary and fallopian tube during cesarean section delivery successfully managed in a resource-limited setting: a case report. [PDF]

Int J Surg Case Rep
Dereje WM, Demilew LE, Worku MA, Agegnehu GT, Mebratu AA, Mengist BA.   +5 more
europepmc   +1 more source

MYRF gene mutation leading to coronary artery anomaly combined with 46,XY sex development disorder, a case report and literature review. [PDF]

BMC Pediatr
Ding J, Lv Z, Zhen Z, Gai Y, Xiao Y.
europepmc   +1 more source