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UnknownPituitary stalk interruption syndrome is characterized by genetic heterogeneity.
Not available
S-EPMC7714207 | biostudies-literature
UnknownExome sequencing in 16 patients with pituitary stalk interruption syndrome: A monocentric study.
Not available
S-EPMC10721018 | biostudies-literature
UnknownPeripheral Precocious Puberty of Ovarian Origin in a Series of 18 Girls: Exome Study Finds Variants in Genes Responsible for Hypogonadotropic Hypogonadism.
Not available
S-EPMC8149944 | biostudies-literature
UnknownLoss-of-function mutation in GATA4 causes anomalies of human testicular development.
Not available
S-EPMC3029689 | biostudies-literature
UnknownAnomalies in Human Sex Determination: Usefulness of a Combined Cytogenetic Approach to Characterize an Additional Case with Xp Functional Disomy Associated with 46,XY Gonadal Dysgenesis
Not available
S-EPMC9976160 | biostudies-literature
UnknownAn ancient protein-DNA interaction underlying metazoan sex determination.
Not available
S-EPMC4476070 | biostudies-literature
UnknownClinical, biological and genetic analysis of prepubertal isolated ovarian cyst in 11 girls.
Not available
S-EPMC2892512 | biostudies-literature
UnknownAutosomal dominant nonsyndromic cleft lip and palate: significant evidence of linkage at 18q21.1.
Not available
S-EPMC1950911 | biostudies-literature
UnknownEvidence for NR2F2/COUP-TFII involvement in human testis development.
Not available
S-EPMC11294483 | biostudies-literature
UnknownIdentification of a Novel Mutation of LAMB3 Gene in a Lybian Patient with Hereditary Epidermolysis Bullosa by Whole Exome Sequencing.
Not available
S-EPMC5383759 | biostudies-literature
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