Exhaustive screening of the 21-hydroxylase gene in a population of hyperandrogenic women

Human Genetics

Volumn 101, Issue 1, 1997, Pages 56-60

  Blanché, Hélène ^a   Vexiau, Patrick ^b   Clauin, Séverine ^a   Le Gall, Isabelle ^a   Fiet, Jean ^b   Mornet, Etienne ^c   Dausset, Jean ^a   Bellanné Chantelot, Christine ^a  

^a FONDATION JEAN DAUSSET CEPH   (France)

^b SAINT LOUIS HOSPITAL   (France)

^c SESEP   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CORTICOTROPIN; DNA; HYDROCORTISONE DERIVATIVE; HYDROXYPROGESTERONE; STEROID 21 MONOOXYGENASE;

ADOLESCENT; ADULT; AMINO ACID SUBSTITUTION; ARTICLE; EXON; FEMALE; GENE MUTATION; GENE REARRANGEMENT; GENE SEQUENCE; GENETIC SCREENING; HETEROZYGOTE; HORMONE BLOOD LEVEL; HUMAN; HUMAN CELL; HYPERANDROGENISM; INTRON; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; PROMOTER REGION; STEROID 21 MONOOXYGENASE DEFICIENCY;

17-ALPHA-HYDROXYPROGESTERONE; ADOLESCENT; ADRENAL HYPERPLASIA, CONGENITAL; ADRENOCORTICOTROPIC HORMONE; ADULT; ALLELES; BASE SEQUENCE; CHILD; CORTODOXONE; DNA PRIMERS; FEMALE; GENETIC COUNSELING; GENETIC SCREENING; GENOTYPE; HETEROZYGOTE; HIRSUTISM; HOMOZYGOTE; HUMANS; HYPERANDROGENISM; MIDDLE AGED; MUTATION; PHENOTYPE; POLYMERASE CHAIN REACTION; STEROID 21-HYDROXYLASE;

EID: 0031440220     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050586     Document Type: Article

References (29)

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