Secondary male hypogonadism and congenital ichthyosis: association of two rare genetic diseases.

Journal article

Peer reviewed

H. T. LYNCH, F. OZER, C. W. MCNUTT, J. E. JOHNSON and N. A. JAMPOLSKY

American journal of human genetics, Vol.12, pp.440-447

12

12/01/1960

PMCID: PMC1932176

PMID: 13764559

Abstract

Genetics

Genetics(clinical)

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Title: Secondary male hypogonadism and congenital ichthyosis
Creators: H. T. LYNCH (Author) - Unknown
F. OZER (Author)
C. W. MCNUTT (Author)
J. E. JOHNSON (Author)
N. A. JAMPOLSKY (Author)
Additional links: Clark, Terry D.; Potter, Joshua D.; Larson, Jennifer M.; Mordeson, John N.; Wierman, Mark J.; Caulfield, J.H.; Chen, S.H.; Cheng, H.D.; Duro, R.; Caufield, J.H.; Chen, S.H.; Cheng, H.D.; Duro, R.; Honavar, V.
Publication Details: American journal of human genetics, Vol.12, pp.440-447
Series: 12
Number of pages: 8
Identifiers: 991005929599102656
Academic Unit: Creighton University
Language: English
Resource Type: Journal article