A molecular and fish approach to determining karyotype and phenotype correlations in six patients with supernumerary marker(22) chromosomes

American Journal of Medical Genetics

Volumn 72, Issue 4, 1997, Pages 440-447

  Crolla, John A ^a   Howard, Peter ^b   Mitchell, Caroline ^a   Long, Fiona L ^a   Dennis, Nicholas R ^c  

^a SALISBURY DISTRICT HOSPITAL   (United Kingdom)

^b LIVERPOOL WOMEN S HOSPITAL   (United Kingdom)

^c PRINCESS ANNE HOSPITAL   (United Kingdom)

Author keywords

Cat eye syndrome; Fluorescence in situ hybridisation; Supernumerary marker(22)

Indexed keywords

ARTICLE; CHROMOSOME 22Q; CHROMOSOME SATELLITE ASSOCIATION; CLINICAL ARTICLE; CYTOGENETICS; DIGEORGE SYNDROME; FEMALE; HUMAN; HUMAN CELL; HUMAN TISSUE; KARYOTYPE; MALE; MOLECULAR GENETICS; NEWBORN; PHENOTYPE; PRIORITY JOURNAL; SUPERNUMERARY CHROMOSOME;

CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; GENETIC HETEROGENEITY; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; PEDIGREE; PHENOTYPE; POLYMERASE CHAIN REACTION;

EID: 0030784523     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19971112)72:4<440::AID-AJMG13>3.0.CO;2-R     Document Type: Article

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