Trisomy 14pter→q21: A case with associated ovarian germ cell tumor and review of the literature

American Journal of Medical Genetics

Volumn 128 A, Issue 1, 2004, Pages 78-84

  Lee Jones, Lisa ^a   Williams, Tom ^b   Little, Elizabeth ^c   Sampson, Julian ^a  

^a CARDIFF UNIVERSITY   (United Kingdom)

^b NEVILL HALL HOSPITAL   (United Kingdom)

^c UNIVERSITY HOSPITAL OF WALES   (United Kingdom)

Author keywords

CGH; Duplication; Ovarian germ cell tumor; Supernumerary marker chromosome; Trisomy 14pter 21

Indexed keywords

KARYOTYPE 48,XXX; UNCLASSIFIED DRUG;

ADOLESCENT; CANCER SUSCEPTIBILITY; CASE REPORT; CHROMOSOME 14P; COMPARATIVE GENOMIC HYBRIDIZATION; DEVELOPMENTAL DISORDER; FACE DYSMORPHIA; FEMALE; GERM CELL TUMOR; HIGH PITCHED CRY; HUMAN; HUMAN CELL; KARYOTYPE; LARYNX DISORDER; MARKER CHROMOSOME; OVARY GERM CELL TUMOR; OVARY TERATOMA; OVARY TUMOR; PRIORITY JOURNAL; REVIEW; SUPERNUMERARY CHROMOSOME; TRISOMY; TRISOMY 14P; TRISOMY X; X CHROMOSOME; ARTICLE; CHROMOSOME 14; CONGENITAL MALFORMATION; FACE; GENETICS; KARYOTYPING; MULTIPLE MALFORMATION SYNDROME; NEOPLASM; NEWBORN;

ABNORMALITIES, MULTIPLE; ADOLESCENT; CHROMOSOMES, HUMAN, PAIR 14; CHROMOSOMES, HUMAN, X; DEVELOPMENTAL DISABILITIES; FACE; FEMALE; HUMANS; INFANT, NEWBORN; KARYOTYPING; NEOPLASMS, GERM CELL AND EMBRYONAL; OVARIAN NEOPLASMS; TRISOMY;

EID: 3042727944     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30076     Document Type: Review

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