Prenatal diagnosis of partial monosomy 3p and partial trisomy 2p in a fetus associated with shortening of the long bones and a single umbilical artery

Prenatal Diagnosis

Volumn 16, Issue 3, 1996, Pages 270-275

  Chen, Chih Ping ^a   Liu, Fen Fen ^a   Jan, Sheau Wen ^a   Lin, Shuan Pei ^a   Lan, Chung Chi ^a  

^a MACKAY MEMORIAL HOSPITAL   (Taiwan)

Author keywords

3p syndrome; partial trisomy 2p; prenatal diagnosis; shortening of the long bones; single umbilical artery

Indexed keywords

ARTICLE; BONE DYSPLASIA; CASE REPORT; CHROMOSOME 2P; CHROMOSOME 3P; CHROMOSOME TRANSLOCATION; CONGENITAL BLOOD VESSEL MALFORMATION; FETUS; HUMAN; HUMAN CELL; MENTAL RETARDATION MALFORMATION SYNDROME; PARTIAL MONOSOMY; PARTIAL TRISOMY; PHENOTYPE; PRIORITY JOURNAL; UMBILICAL ARTERY;

ABNORMALITIES, MULTIPLE; ADULT; AMNIOCENTESIS; BONE AND BONES; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 2; CHROMOSOMES, HUMAN, PAIR 3; FACIAL BONES; FEMALE; FETAL DISEASES; HUMANS; KARYOTYPING; MALE; MONOSOMY; PREGNANCY; PRENATAL DIAGNOSIS; SKULL; TRISOMY; UMBILICAL ARTERIES;

EID: 0029935520     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199603)16:3<270::AID-PD836>3.0.CO;2-0     Document Type: Article

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