A paternally inherited terminal deletion, del(8)(p23.1)pat, detected prenatally in an amniotic fluid sample: A review of deletion 8p23.1 cases

Prenatal Diagnosis

Volumn 19, Issue 9, 1999, Pages 868-872

  Reddy, K S ^a  

^a QUEST DIAGNOSTICS NICHOLS INSTITUTE   (United States)

Author keywords

Clinical findings; del(8)(p23.1); FISH

Indexed keywords

ADULT; AMNION CELL; AMNION FLUID ANALYSIS; ARTICLE; CHROMOSOME 8P; CLINICAL ARTICLE; CYTOGENETICS; DEVELOPMENTAL DISORDER; FEMALE; FETUS ECHOGRAPHY; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; HEART ATRIUM SEPTUM DEFECT; HEART VENTRICLE SEPTUM DEFECT; HUMAN; INFANT; INHERITANCE; KARYOTYPE; MALE; MICROCEPHALY; NEWBORN; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; PULMONARY VALVE STENOSIS; SCHOOL CHILD; SPONTANEOUS ABORTION;

ADULT; AMNIOTIC FLUID; CHILD; CHROMOSOMES, HUMAN, PAIR 8; FATHERS; FEMALE; HUMANS; INFANT; INFANT, NEWBORN; MALE; PREGNANCY; PRENATAL DIAGNOSIS; RETROSPECTIVE STUDIES;

POMACANTHUS MACULOSUS;

EID: 0032854607     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199909)19:9<868::AID-PD641>3.0.CO;2-A     Document Type: Article

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