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Landmark studies have shown that mutations in kisspeptin and the kisspeptin receptor (Kiss1r) result in reproductive dysfunction… Expand CONTEXT
Mutations in TAC3 and TACR3 (encoding neurokinin B and its receptor) have been identified in Turkish patients with… Expand CONTEXT
Both biallelic and monoallelic mutations in PROK2 or PROKR2 have been found in Kallmann syndrome (KS).
The… Expand BACKGROUND
Kallmann's syndrome (KS) is a clinically and genetically heterogeneous disorder consisting of idiopathic… Expand Larval digenetic trematodes commonly castrate their first intermediate hosts, and should therefore impose strong selection on the… Expand As our knowledge of the molecular mechanisms underlying idiopathic hypogonadotropic hypogonadism (IHH) expands, it becomes… Expand We report, in detail, a new form of familial dwarfism, including its phenotypic features, hormonal profile, and molecular basis… Expand A family of 5 affected male infants in 2 generations with an X‐linked pattern of inheritance is described. All affected infants… Expand Of fourteen boys with microphallus who were studied consecutively, nine had hypopituitarism that might otherwise have not been… Expand The association of hypoglycemia and microphallus in the male neonate is presumptive evidence of congenital hypopituitarism. This… Expand