Results 131 to 140 of about 12,853 (226)

Supplementary Material for: A Small Supernumerary Xp Marker Chromosome Including Genes NR0B1 and MAGEB Causing Partial Gonadal Dysgenesis and Gonadoblastoma

open access: gold, 2021
Nishi M.Y.   +8 more
openalex   +1 more source

A rare case of mixed gonadal dysgenesis in adulthood: diagnostic delay and unique outcomes. [PDF]

open access: yesJ Surg Case Rep, 2023
Rueangket P   +3 more
europepmc   +1 more source

Laparoscopy versus ultrasonography for the evaluation of Müllerian duct remnants in male patients with disorder of sex differentiation

open access: yesEgyptian Pediatric Association Gazette
Background The diagnosis of male differences of sex development is a challenging multidisciplinary team task, that requires external genital evaluation, karyotyping, hormonal profiling, radiological work up and frequently diagnostic laparoscopy and ...
Mohamed Sayed Abd El-Monsif   +4 more
doaj   +1 more source

DHX37 and NR5A1 Variants Identified in Patients with 46,XY Partial Gonadal Dysgenesis. [PDF]

open access: yesLife (Basel), 2023
de Oliveira FR   +9 more
europepmc   +1 more source

ACTH bioassay with isolated rat adrenal cells: ACTH activity of the porcins lipotropic peptide B [PDF]

open access: yes, 1974
Baur, X.   +5 more
core   +1 more source

Pregnancy and labor in gonadal dysgenesis (Case report)

open access: hybrid, 2000
Е. В. Исакова   +3 more
openalex   +2 more sources

Disruption of the topologically associated domain at Xp21.2 is related to 46,XY gonadal dysgenesis. [PDF]

open access: yesJ Med Genet, 2023
Meinel JA   +11 more
europepmc   +1 more source

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