Inherited interstitial deletion of chromosomes 5p and 16q without apparent phenotypic effect: Further confirmation

Prenatal Diagnosis

Volumn 20, Issue 2, 2000, Pages 144-148

  Hand, Jennifer L ^a   Michels, Virginia V ^a   Marinello, Michelle J ^b   Ketterling, Rhett P ^a   Jalal, Syed M ^a  

^a MAYO CLINIC   (United States)

^b Genetic Diagn Laboratories Inc   (United States)

Author keywords

Chromosome; Interstitial deletion; Normal phenotype

Indexed keywords

ADULT; AMNIOCENTESIS; ARTICLE; CASE REPORT; CHROMOSOME 16Q; CHROMOSOME DELETION 5; CHROMOSOME HIGH RESOLUTION BANDING ANALYSIS; DISORDERS OF PEROXISOMAL FUNCTIONS; FEMALE; FETUS; GENETIC COUNSELING; HUMAN; INTERSTITIAL CHROMOSOME DELETION; MALE; MATERNAL AGE; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

ADULT; AMNIOCENTESIS; CHROMOSOME PAINTING; CHROMOSOMES, HUMAN, PAIR 16; CHROMOSOMES, HUMAN, PAIR 5; FEMALE; GENE DELETION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; MATERNAL AGE; PHENOTYPE; PREGNANCY; PREGNANCY, HIGH-RISK;

RAPHIA FRATER;

EID: 0033976407     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(200002)20:2<144::AID-PD770>3.0.CO;2-9     Document Type: Article

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