Uniparental disomy in humans: Development of an imprinting map and its implications for prenatal diagnosis

Human Molecular Genetics

Volumn 4, Issue REV. ISS., 1995, Pages 1757-1764

  Ledbetter, David H ^a   Engel, Eric ^b  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b UNIVERSITY OF GENEVA   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

AMNIOCENTESIS; AUTOSOMAL RECESSIVE DISORDER; CHORION VILLUS SAMPLING; CHROMOSOME MOSAICISM; DISOMY; GENE MAPPING; GENOME IMPRINTING; HOMOZYGOSITY; HUMAN; MARKER CHROMOSOME; MEIOSIS; MONOSOMY; PHENOTYPE; PLACENTA; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RECIPROCAL CHROMOSOME TRANSLOCATION; REVIEW; ROBERTSONIAN CHROMOSOME TRANSLOCATION; TRISOMY;

ANIMALIA; ROBERTSONIA;

EID: 0029162269     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/4.suppl_1.1757     Document Type: Review

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