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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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Published on: August 20, 2019

[X-linked Kallmann's syndrome: intra and interfamilial heterogeneity]

Alfonso Vidal1, Lourdes Loidi, Esmeralda Colino

  • 1Unidad de Endocrinología Pediátrica, Hospital Universitario Ramón y Cajal, Madrid, Spain.

Medicina Clinica
|June 15, 2007
PubMed
Abstract

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