Prenatal diagnosis of trisomy 18p and distal 21q22.3 deletion

Prenatal Diagnosis

Volumn 23, Issue 9, 2003, Pages 758-761

  Chen, Chih Ping ^a,b   Chern, Schu Rern ^a   Lee, Chen Chi ^a   Chen, Li Feng ^a   Chin, Daniel T H ^a   Tzen, Chin Yuan ^a   Wang, Wayseen ^a  

^a MACKAY MEMORIAL HOSPITAL   (Taiwan)

^b NATIONAL YANG MING UNIVERSITY   (Taiwan)

Author keywords

21q22.3 deletion; Holoprosencephaly; Polymorphic microsatellite markers; Prenatal diagnosis; Trisomy 18p

Indexed keywords

ADULT; AMNIOCENTESIS; AMNION CELL; AMNION FLUID CYTOLOGY; ARTICLE; CASE REPORT; CENTROMERE; CHROMOSOME 18; CHROMOSOME 21; CHROMOSOME 21Q; CHROMOSOME ANALYSIS; CHROMOSOME ARM; CHROMOSOME BREAKAGE; CHROMOSOME DELETION; CHROMOSOME DELETION 21Q; CHROMOSOME SATELLITE; CLINICAL FEATURE; CLINODACTYLY; ECHOGRAPHY; FEMALE; FETUS; GENETIC ANALYSIS; GENETIC MARKER; GESTATIONAL AGE; HETEROZYGOTE; HIGH ARCHED PALATE; HOLOPROSENCEPHALY; HUMAN; HUMAN CELL; HUMAN TISSUE; HYPERTELORISM; KARYOTYPING; MALE; MICROGNATHIA; MONOSOMY; MONOSOMY 21Q; NEWBORN; PHENOTYPE; PREGNANCY; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RECIPROCAL CHROMOSOME TRANSLOCATION; TRISOMY 18; TRISOMY 18P;

ABORTION, INDUCED; ADULT; CHROMOSOMES, HUMAN, PAIR 18; CHROMOSOMES, HUMAN, PAIR 21; DIAGNOSIS, DIFFERENTIAL; FEMALE; GENETIC COUNSELING; HOLOPROSENCEPHALY; HUMANS; PREGNANCY; PREGNANCY TRIMESTER, SECOND; PRENATAL DIAGNOSIS; TRISOMY;

POMACANTHUS MACULOSUS;

EID: 0141522809     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.684     Document Type: Article

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