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Volumn 28, Issue 5, 2008, Pages 450-453

Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand-foot malformation associated with partial monosomy 4p (4p16.1→pter) and partial trisomy 10q (10q25.1→qter)

Author keywords

Partial monosomy 4p; Partial trisomy 10q; Prenatal diagnosis; Split hand foot malformation (SHFM); Wolf Hirschhorn syndrome (WHS)

Indexed keywords

ADULT; AMNIOCENTESIS; ANAMNESIS; ARTICLE; BACTERIAL ARTIFICIAL CHROMOSOME; CASE REPORT; CHROMOSOME ANALYSIS; CHROMOSOME DELETION 4; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL MALFORMATION; FEMALE; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; GESTATIONAL AGE; HAND FOOT SYNDROME; HUMAN; KARYOTYPE; PARTIAL MONOSOMY; PARTIAL TRISOMY 10; PRIORITY JOURNAL; ULTRASOUND; WOLF HIRSCHHORN SYNDROME;

EID: 45249096508     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.1993     Document Type: Article
Times cited : (11)

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