Results 141 to 150 of about 23,557 (205)

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

open access: yesClin Exp Reprod Med
Maghsoomi Z   +7 more
europepmc   +1 more source

MLC1 alteration in human iPSCs give rise to disease-like cellular vacuolation phenotype in the astrocyte lineage. [PDF]

open access: yesOrphanet J Rare Dis
Sharma S   +12 more
europepmc   +1 more source

Experimental pulmonary arterial hypertension in mice with a pathogenic SOX17 variant. [PDF]

open access: yesSci Rep
Shinya Y   +8 more
europepmc   +1 more source

The Role of WWOX Gene Variant in Hypospadias and 46,XY Disorders of Sexual Development. [PDF]

open access: yesReprod Sci
Denkboy Ongen Y   +5 more
europepmc   +1 more source

Sertoli cells as a hub in testicular development and male reproductive. [PDF]

open access: yesFront Cell Dev Biol
Feng X   +9 more
europepmc   +1 more source

Androgen activity in the male embryonic hindbrain drives lethal PFA ependymoma. [PDF]

open access: yesNature
Zhang J   +85 more
europepmc   +1 more source

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