Prenatal diagnosis of partial trisomy 4q26-qter and monosomy for the Wolf-Hirschhorn critical region in a fetus with split hand malformation

Prenatal Diagnosis

Volumn 20, Issue 4, 2000, Pages 349-352

  Petek, Erwin ^a   Wagner, Klaus ^a   Steiner, Horst ^b   Schaffer, Heinz ^b   Kroisel, Peter M ^a  

^a UNIVERSITY OF GRAZ   (Austria)

^b University Hospital Salzburg   (Austria)

Author keywords

4q26 qter; FISH analysis; Microtia; Partial trisomy; Split hands; Wolf Hirschhorn syndrome

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 4P; CHROMOSOME 4Q; CHROMOSOME G BAND; CHROMOSOME PAINTING; CLINICAL FEATURE; CONGENITAL HEART MALFORMATION; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; HAND MALFORMATION; HUMAN; HUMAN CELL; HUMAN TISSUE; HYPOPLASIA; KARYOTYPE; KIDNEY ANOMALY; MALE; MICROTIA; MONOSOMY; NEWBORN; PARTIAL TRISOMY 4; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; THORAX DISEASE; WOLF HIRSCHHORN SYNDROME; YEAST ARTIFICIAL CHROMOSOME;

ABNORMALITIES, MULTIPLE; ADULT; CHROMOSOMES, HUMAN, PAIR 4; CYTOGENETIC ANALYSIS; FATAL OUTCOME; FEMALE; FETAL GROWTH RETARDATION; HAND DEFORMITIES, CONGENITAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MIDDLE AGED; MONOSOMY; PREGNANCY; SYNDROME; TRISOMY; ULTRASONOGRAPHY, PRENATAL;

CANIS; MICROTIA;

EID: 0034074244     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(200004)20:4<349::AID-PD808>3.0.CO;2-B     Document Type: Article

References (7)

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