Results 181 to 190 of about 21,834 (238)

Transsexualism and the Binary Divide: Determining Sex Using Objective Criteria [PDF]

, 2015
Staver, Matthew D.
core   +1 more source

Clinical Characteristics and Management of Two Cases of Complete Androgen Insensitivity Syndrome With Germ Cell Tumors. [PDF]

Cancer Rep (Hoboken)
Wang F, Wang D, Li J, Xing N.
europepmc   +1 more source

STARD9 and CDK5RAP2-Novel Candidate Genes for 46,XY Complete Gonadal Dysgenesis. [PDF]

Int J Mol Sci
Sirokha D, Rayevsky A, Kalynovskyi V, Khalangot M, Samson O, Gorodna O, Kwiatkowska K, Mayere C, Lemanska Z, Kunik A, Nef S, Kusz-Zamelczyk K, Livshits L.   +12 more
europepmc   +1 more source

Functional Validation of a Novel <italic>PBX1</italic> Missense Variant in a 46,XY Girl.

Sex Dev
Tsai MC, Weng YH, Wang YC, Chou YY, Chang KC, Chen PC.   +5 more
europepmc   +1 more source

Isodicentric Y chromosome with SRY duplication in a female with complete gonadal dysgenesis. [PDF]

Mol Cytogenet
Salmaninejad A, Yaghoubi Z, Haghzad T, Latifi M, Bayat R, Esnaashari S, Dalili S.   +6 more
europepmc   +1 more source

A novel heterozygous mutation of BCL11B gene causes neurodevelopmental disorder and middle type hypospadias in a Chinese boy with 5 years follow-up. [PDF]

Neurogenetics
Liu Y, Pan Z, Shi J, Jiang M, Li J.
europepmc   +1 more source

Advanced-Stage Gonadal Dysgerminoma in a Patient With a Previous Diagnosis of Familial Swyer Syndrome: A Very Rare Genetic Entity. [PDF]

Case Rep Med
Oğlak SC, Söğütçü N, Akgöl S, Adıgüzel Ö, Ateş Eminoğlu HE, Güzel G, Balcı V, Acar E, Acar A, Bozan F.   +9 more
europepmc   +1 more source

Uncontrolled hypertension in siblings: an unsuspected diagnosis. [PDF]

AJOG Glob Rep
Aleem S, Kumar S, Guddeti A, Hari Kumar K.   +3 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

DHX37 variants in patients with 46,XY disorders or differences of sex development. [PDF]

Hum Genome Var
Katoh-Fukui Y, Saito D, Narumi H, Hattori A, Igarashi M, Uehara E, Shima H, Kanno J, Hasegawa Y, Horikawa R, Nagasaki K, Fukami M.   +11 more
europepmc   +1 more source