A homozygous mutation in the luteinizing hormone receptor causes partial Leydig cell hypoplasia: correlation between receptor activity and phenotype

JWM Martens, M Verhoef-Post, N Abelin… - Molecular …, 1998 - academic.oup.com
Leydig cell hypoplasia (LCH) is characterized by a decreased response of the Leydig cells
to LH. As a result, patients with this syndrome display aberrant male development ranging …
被引用次数：141 相关文章
[PDF] archive.org

[PDF][PDF] A Homozygous Mutation in the Luteinizing Hormone Receptor Causes Partial Leydig Cell Hypoplasia: Correlation between Receptor Activity and Phenotype

JWM Martens, M Verhoef-Post, N Abelin, M Ezabella… - 1998 - scholar.archive.org
Leydig cell hypoplasia (LCH) is characterized by a decreased response of the Leydig cells
to LH. As a result, patients with this syndrome display aberrant male development ranging …

A homozygous mutation in the luteinizing hormone receptor causes partial Leydig cell hypopla phenotype

J Martens, M Verhoef-Post, N Abelin… - Molecular …, 1998 - repub.eur.nl
Leydig cell hypoplasia (LCH) is characterized by a decreased response of the Leydig cells
to LH. As a result, patients with this syndrome display aberrant male development ranging …
[PDF] researchgate.net

[PDF][PDF] A Homozygous Mutation in the Luteinizing Hormone Receptor Causes Partial Leydig Cell Hypoplasia: Correlation between Receptor Activity and Phenotype

JWM Martens, M Verhoef-Post, N Abelin, M Ezabella… - 1998 - researchgate.net
Leydig cell hypoplasia (LCH) is characterized by a decreased response of the Leydig cells
to LH. As a result, patients with this syndrome display aberrant male development ranging …

[引用][C] A Homozygous Mutation in the Luteinizing Hormone Receptor Causes Partial Leydig Cell Hypoplasia: Correlation between Receptor Activity and Phenotype

JWM Martens - Molecular Endocrinology, 1998 - cir.nii.ac.jp
A Homozygous Mutation in the Luteinizing Hormone Receptor Causes Partial Leydig Cell
Hypoplasia: Correlation between Receptor Activity and Phenotype | CiNii Research CiNii 国立 …
[PDF] academia.edu

[PDF][PDF] A Homozygous Mutation in the Luteinizing Hormone Receptor Causes Partial Leydig Cell Hypoplasia: Correlation between Receptor Activity and Phenotype

JWM Martens, M Verhoef-Post, N Abelin, M Ezabella… - 1998 - academia.edu
Leydig cell hypoplasia (LCH) is characterized by a decreased response of the Leydig cells
to LH. As a result, patients with this syndrome display aberrant male development ranging …

[引用][C] A homozygous mutation in the luteinizing hormone receptor causes partial Leydig cell hypoplasia: correlation between receptor activity and phenotype

JW Martens, M Verhoef-Post, N Abelin, M Ezabella… - 1998 - repository.ubn.ru.nl
A homozygous mutation in the luteinizing hormone receptor causes partial Leydig cell
hypoplasia: correlation between receptor activity and phenotype Toggle navigation …

[引用][C] A homozygous mutation in the luteinizing hormone receptor causes partial leydig cell hypoplasia: correlation between receptor activity and phenotype

JWM Martens, MV Post, NMA Abelin… - Molecular …, 1998 - repositorio.usp.br
ReP USP - Detalhe do registro: A homozygous mutation in the luteinizing hormone receptor
causes partial leydig cell hypoplasia: correlation between receptor activity and phenotype …

A homozygous mutation in the luteinizing hormone receptor causes partial Leydig cell hypoplasia: correlation between receptor activity and phenotype.

JW Martens, M Verhoef-Post, N Abelin… - Molecular …, 1998 - europepmc.org
Leydig cell hypoplasia (LCH) is characterized by a decreased response of the Leydig cells
to LH. As a result, patients with this syndrome display aberrant male development ranging …

A homozygous mutation in the luteinizing hormone receptor causes partial Leydig cell hypoplasia: correlation between receptor activity and phenotype

JW Martens, M Verhoef-Post… - Molecular …, 1998 - pubmed.ncbi.nlm.nih.gov
Leydig cell hypoplasia (LCH) is characterized by a decreased response of the Leydig cells
to LH. As a result, patients with this syndrome display aberrant male development ranging …