Retinoblastoma in association with the chromosome breakage syndromes Fanconi's anaemia and Bloom's syndrome: clinical and cytogenetic findings

Clinical Genetics

Volumn 47, Issue 6, 1995, Pages 311-317

  Gibbons, Barbara ^a   Scott, David ^a   Hungerford, John L ^a   Cheung, Kan Luk ^a   Harrison, Christine ^a   Attard‐Montalto, Simon ^a   Evans, Miles ^a   Birch, Jillian M ^b   Kingston, Judith E ^a  

^a ST BARTHOLOMEW S HOSPITAL   (United Kingdom)

^b CHRISTIE HOSPITAL   (United Kingdom)

Author keywords

Bloom's syndrome; chromosome breakage; Fanconi's anaemia; mitomycin C; retinoblastoma; X rays

Indexed keywords

MITOMYCIN C;

ARTICLE; BLOOM SYNDROME; CASE REPORT; CHILD; CHROMOSOME ANALYSIS; CHROMOSOME BREAKAGE; CHRONIC MYELOID LEUKEMIA; CLINICAL FEATURE; DISEASE ASSOCIATION; FACE MALFORMATION; FANCONI ANEMIA; FEMALE; GROWTH DISORDER; HUMAN; HUMAN CELL; LYMPHOCYTE; MICROCEPHALY; MYELODYSPLASIA; PIGMENT DISORDER; PRESCHOOL CHILD; PRIORITY JOURNAL; RADIATION MUTAGENESIS; RETINOBLASTOMA; SKIN PIGMENTATION; X RAY;

BLOOM SYNDROME; CASE REPORT; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOMES; DNA; EYE NEOPLASMS; FANCONI ANEMIA; FEMALE; HUMAN; INFANT; INFANT, NEWBORN; LEUKEMIA, MYELOCYTIC, ACUTE; LYMPHOCYTES; MITOMYCIN; RETINOBLASTOMA; SISTER CHROMATID EXCHANGE; SUPPORT, NON-U.S. GOV'T;

EID: 0029039558     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1995.tb03971.x     Document Type: Article

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