Kallmann syndrome in a patient with congenital spherocytosis and an interstitial 8p11.2 deletion

American Journal of Medical Genetics

Volumn 108, Issue 4, 2002, Pages 315-318

  Vermeulen, Stefan ^a   Messiaen, Ludwine ^a   Scheir, Petra ^a   De Bie, Sylvia ^a   Speleman, Frank ^a   De Paepe, Anne ^a  

^a GHENT UNIVERSITY HOSPITAL   (Belgium)

Author keywords

8p11.2 deletion; Congenital spherocytosis; Kallmann syndrome

Indexed keywords

ANKYRIN; ANKYRIN 1; UNCLASSIFIED DRUG;

ADOLESCENT; ANOSMIA; ARTICLE; CASE REPORT; CHROMOSOME DELETION; CLINICAL FEATURE; CYTOGENETICS; GENE MUTATION; HEREDITARY SPHEROCYTOSIS; HUMAN; HYPOGONADOTROPIC HYPOGONADISM; KALLMANN SYNDROME; MALE; MOLECULAR GENETICS; PHENOTYPE; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; ADOLESCENT; CHROMOSOME BANDING; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 8; GROWTH DISORDERS; HUMANS; KALLMANN SYNDROME; KARYOTYPING; MALE; MICROSATELLITE REPEATS; SPHEROCYTOSIS, HEREDITARY; SYNDROME;

EID: 0036532031     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10295     Document Type: Article

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