Brief clinical report: Unique case of trisomy 2p24.3-pter with no associated monosomy

American Journal of Medical Genetics

Volumn 101, Issue 1, 2001, Pages 50-54

  Roggenbuck, Jennifer A ^a   Fink, James M ^a   Mendelsohn, Nancy J ^a  

^a HENNEPIN COUNTY MEDICAL CENTER   (United States)

Author keywords

Human chromosome 2; Neural tube gene localization; Trisomy 2p syndrome

Indexed keywords

ARTICLE; BIRTH DEFECT; CASE REPORT; CHILD; CHROMOSOME ANALYSIS; CLINICAL FEATURE; DISEASE COURSE; FACE DYSMORPHIA; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE LOCUS; GENETIC COUNSELING; HUMAN; MONOSOMY; NEURAL TUBE DEFECT; PRIORITY JOURNAL; PROGNOSIS; PSYCHOMOTOR RETARDATION; TRISOMY; TRISOMY 2P; CHROMOSOME 2; KARYOTYPING; MENTAL DEFICIENCY; METHODOLOGY; PHENOTYPE;

CHILD; CHROMOSOMES, HUMAN, PAIR 2; CYTOGENETIC ANALYSIS; FEMALE; GENETIC COUNSELING; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MENTAL RETARDATION; MONOSOMY; PHENOTYPE; TRISOMY;

EID: 0035371157     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.1309     Document Type: Article

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