Translocation between chromosomes 6 and 15 (45,XX, t(6;15)(q25;ql 1.2)) with further evidence for lack of imprinting of the insulin-like growth factor II/mannose-6-phosphate receptor in humans

Journal of Medical Genetics

Volumn 33, Issue 1, 1996, Pages 42-46

  Treacy, Eileen ^a,b   Polychronakos, Constantin ^a   Vekemans, Michel ^a,b,c   Eydoux, Patrice ^a,b   Blaichman, Shirley ^a   Scarpelli, Helene ^a,b   Ross, Michelle ^a   Xu, Yongqin ^a   Der Kaloustian, Vazken M ^a,b  

^a MONTREAL CHILDREN S HOSPITAL   (Canada)

^b MCGILL UNIVERSITY   (Canada)

^c INSTITUT DE RECHERCHES INTERNATIONALES SERVIER   (France)

Author keywords

15 translocation; Chromosome 6; Imprinting; Mannose 6 phosphate receptor

Indexed keywords

SOMATOMEDIN B RECEPTOR;

ADULT; ARTICLE; CASE REPORT; CHROMOSOME TRANSLOCATION 15; CHROMOSOME TRANSLOCATION 6; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DOSAGE; GENE LOSS; GROWTH RETARDATION; HUMAN; HUMAN CELL; MICROCEPHALY; PRADER WILLI SYNDROME; PRIORITY JOURNAL; RECEPTOR GENE;

ADULT; BASE SEQUENCE; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 15; CHROMOSOMES, HUMAN, PAIR 6; DNA PRIMERS; FEMALE; GENETIC MARKERS; GENOMIC IMPRINTING; HUMANS; INSULIN-LIKE GROWTH FACTOR I; MIDDLE AGED; MOLECULAR SEQUENCE DATA; RECEPTOR, IGF TYPE 2; TRANSLOCATION, GENETIC;

EID: 0030063014     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (17)

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