The phenotypic spectrum of trisomy 2: Report of two new cases

Clinical Dysmorphology

Volumn 18, Issue 4, 2009, Pages 201-204

  Mihci, Ercan ^a   Velagaleti, Gopalrao V N ^a   Ensenauer, Regina ^a   Babovic Vuksanovic, Dusica ^a  

^a Mayo Clinic   (United States)

Author keywords

Acardiac and acranial fetus; Mosaicism; Trisomy 2

Indexed keywords

ACARDIUS; ARTICLE; CASE REPORT; CHILD; CHROMOSOME ANALYSIS; CONGENITAL MALFORMATION; FEMALE; FETUS; HUMAN; MENTAL RETARDATION MALFORMATION SYNDROME; MOSAICISM; MULTIPLE MALFORMATION SYNDROME; PALLISTER KILLIAN SYNDROME; PRIORITY JOURNAL; TRISOMY; TRISOMY 2; ADULT; GENETICS; HUMAN CHROMOSOME; NEWBORN; PATHOLOGY; PHENOTYPE; PREGNANCY; PRESCHOOL CHILD;

ADULT; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN; FEMALE; FETUS; HUMANS; INFANT, NEWBORN; PHENOTYPE; PREGNANCY; TRISOMY;

EID: 70449729969     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/MCD.0b013e32832d0639     Document Type: Article

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