Linkage of congenital isolated adrenocorticotropic hormone deficiency to the corticotropin releasing hormone locus using simple sequence repeat polymorphisms

American Journal of Medical Genetics

Volumn 62, Issue 3, 1996, Pages 262-267

  Kyllo, Jennifer H ^a,d   Collins, Malia M ^a   Vetter, Kimberly L ^a   Cuttler, Leona ^b   Rosenfield, Robert L ^c   Donohoue, Patricia A ^a  

^a UNIVERSITY OF IOWA   (United States)

^b CASE WESTERN RESERVE UNIVERSITY   (United States)

^c UNIVERSITY OF CHICAGO   (United States)

^d UNIVERSITY OF IOWA HOSPITALS AND CLINICS   (United States)

Author keywords

adrenocorticotropic hormone; corticotropin releasing hormone; linkage analysis; simple sequence repeat markers

Indexed keywords

CORTICOTROPIN; CORTICOTROPIN RELEASING FACTOR; HYDROCORTISONE;

ADOLESCENT; ARTICLE; CASE REPORT; CHILD; CLINICAL FEATURE; CORTICOTROPIN DEFICIENCY; DNA POLYMORPHISM; FEMALE; GENE ISOLATION; GENETIC LINKAGE; GENETIC SCREENING; HUMAN; MALE; PRESCHOOL CHILD; PRIORITY JOURNAL;

ADOLESCENT; ADRENAL CORTEX DISEASES; ADRENOCORTICOTROPIC HORMONE; BLOTTING, SOUTHERN; CHROMOSOME MAPPING; CORTICOTROPIN-RELEASING HORMONE; FEMALE; HUMANS; LINKAGE (GENETICS); MALE; PEDIGREE; POLYMORPHISM, GENETIC; PROTEIN PRECURSORS; REPETITIVE SEQUENCES, NUCLEIC ACID;

EID: 0029985387     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19960329)62:3<262::AID-AJMG11>3.0.CO;2-I     Document Type: Article

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