Interstitial deletions without phenotypic effect: Prenatal diagnosis of a new family and brief review

Prenatal Diagnosis

Volumn 11, Issue 6, 1991, Pages 411-416

  Barber, John C K ^a   Mahl, Harjit ^a   Portch, Janet ^a   Crawfurd, Martin D'A ^a  

^a NORTHWICK PARK HOSPITAL   (United Kingdom)

Author keywords

Chromosome 11; Chromosome abnormality; Interstitial deletion; Normal phenotype; Prenatal diagnosis

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 11P; FEMALE; FETUS; GENETIC COUNSELING; HUMAN; HUMAN CELL; INTERSTITIAL CHROMOSOME DELETION; NORMAL HUMAN; PARTIAL MONOSOMY; PEDIGREE; PHENOTYPE; PRENATAL DIAGNOSIS;

ADULT; AMNIOCENTESIS; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 11; FEMALE; GENOTYPE; HUMAN; KARYOTYPING; PHENOTYPE; PREGNANCY;

EID: 0025760897     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.1970110613     Document Type: Article

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