Results 91 to 100 of about 9,834 (152)

A lightweight DSD-UNet-based method for clustered litchi segmentation. [PDF]

Front Plant Sci
Tan Z, Huang Y, Ye D.
europepmc   +1 more source

Uncovering Hidden Genetic Contributors to 46,XY Disorders of Sex Development Through Phenotype-Driven Rare Variant Assessment: A Pilot Study. [PDF]

Genes (Basel)
Tang Y, Chen Y, Zhang Q, Tang J, Ding Y, Li J, Yu T, Wang X.   +7 more
europepmc   +1 more source

Implications of dominance deviations for reproductive and morphological traits in the genetic management of the Pura Raza Española horse. [PDF]

Genet Sel Evol
Perdomo-González DI, Valera M, Molina A, Azor P, Sánchez JP.   +4 more
europepmc   +1 more source

A Likely Diagnosis of Familial Partial Androgen Insensitivity Syndrome in Three 46, XY Siblings With Ambiguous Genitalia: A Case Series. [PDF]

Clin Case Rep
Ali T, Javaid MH, Memon SF, Memon ZF, Iqbal M, Afridi S, Soroush AR, Khan AI, Ahmad N, Afridi NA, Ali Z.   +10 more
europepmc   +1 more source

Refining the diagnosis of 46,XY disorders of sex development: insight from whole-exome sequencing. [PDF]

Orphanet J Rare Dis
Błaszczyk E, Więcek M, Jazela-Stanek A, Kudela G, Koszutski T, Kowalczyk K, Sikora J, Wiernik A, Żarczyńska M, Kempińska W, Bielska-Brodziak A, Gawlik-Starzyk A.   +11 more
europepmc   +1 more source

PEG-rhGH successfully improved the height of a patient with rare 45,X[40]/46,XY[31] disorder of sex development: the first reported case. [PDF]

Transl Pediatr
Li S, Ge R, Liao N, Su Y, Lei C, Hu S, Wang Y, Ren Y.   +7 more
europepmc   +1 more source

Discordant Gender Identity and Surgical Goals in Two Adults with Comparable Ambiguous Genitalia: Two Case Reports from a Resource-Limited Setting. [PDF]

Cureus
Ainomugisha B, Kajabwangu R, Byamukama O, Kato KP, Geissbuhler V, Kayondo M.   +5 more
europepmc   +1 more source

Conundrum resolved by optical genome mapping in a 46,XY girl with difference in sex development and skeletal anomalies. [PDF]

JCEM Case Rep
Daghsni M, Guo F, Forsyth R, Reyes-Múgica M, Yatsenko SA, Witchel SF.   +5 more
europepmc   +1 more source

GFPT1 as a cross-ancestry validated target for degenerative spinal disease: genetic association in a Chinese cohort and functional characterization in zebrafish. [PDF]

Commun Biol
Yang B, Li F, Zhang Y, Zhang F, Wang Z, Da Y, Yang X, Xing W, Tian J.   +8 more
europepmc   +1 more source

Incidental discovery of neglected 11β-hydroxylase deficiency causing 46,XX disorder of sex development in a 35-year-old adult: A radiologically driven diagnosis. [PDF]

Radiol Case Rep
Abouchiba S, Ennejjari N, Ouazzani H, Chaouche I, Akammar A, Haloua M, Alami B, Lamrani MYA, Boubbou M, Maaroufi M, El Bouardi N.   +10 more
europepmc   +1 more source