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3,371
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A family with hypogonadotropic hypogonadism and mutations in the gonadotropin-releasing hormone receptor.
Author(s):
G Schaison
,
C. J. S. Young
,
E Milgrom
,
P. Chanson
,
R Genet
,
Paulo N. Rosa
,
M Misrahi
Publication date:
1997-11-27
Journal:
The New England journal of medicine
Keywords:
Adult
,
Amino Acid Sequence
,
Base Sequence
,
Female
,
Gonadotropin-Releasing Hormone
,
metabolism
,
Gonadotropins
,
deficiency
,
Heterozygote
,
Humans
,
Hypogonadism
,
genetics
,
Male
,
Pedigree
,
Point Mutation
,
Receptors, LHRH
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PubMed
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There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.
Related collections
Karger: Endocrinology
Author and article information
Journal
PubMed ID::
9371856
DOI::
10.1056/NEJM199711273372205
ScienceOpen disciplines:
Chemistry
Keywords:
Adult
,
Amino Acid Sequence
,
Base Sequence
,
Female
,
Gonadotropin-Releasing Hormone
,
metabolism
,
Gonadotropins
,
deficiency
,
Heterozygote
,
Humans
,
Hypogonadism
,
genetics
,
Male
,
Pedigree
,
Point Mutation
,
Receptors, LHRH
Data availability:
ScienceOpen disciplines:
Chemistry
Keywords:
Adult
,
Amino Acid Sequence
,
Base Sequence
,
Female
,
Gonadotropin-Releasing Hormone
,
metabolism
,
Gonadotropins
,
deficiency
,
Heterozygote
,
Humans
,
Hypogonadism
,
genetics
,
Male
,
Pedigree
,
Point Mutation
,
Receptors, LHRH
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