Paternal origin of 11p15 duplications in the Beckwith-Wiedemann syndrome
- 1 January 1992
- journal article
- case report
- Published by Elsevier in Cancer Genetics and Cytogenetics
- Vol. 58 (1) , 66-70
- https://doi.org/10.1016/0165-4608(92)90136-v
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Loss of chromosome 11p alleles in cultured cells derived from Wilms' tumoursBritish Journal of Cancer, 1989
- Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinomaHuman Genetics, 1989
- A Comprehensive and Critical Assessment of Overgrowth and Overgrowth SyndromesPublished by Springer Nature ,1989
- Genomic imprinting and genetic disorders in manTrends in Genetics, 1989
- Detection of human papillomavirus DNA in biopsies of human oral tissueBritish Journal of Cancer, 1987
- Wiedemann-Beckwith syndrome: Cancer predisposition and chromosome 11Cancer Genetics and Cytogenetics, 1986
- Burkitt-like lymphoma in an English child: Characterisation of tumour biopsy cells and of the derived tumour cell lineBritish Journal of Cancer, 1986
- Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two casesHuman Genetics, 1984
- Abnormality of chromosome 11 in patients withfeatures of Beckwith-Wiedemann syndromeThe Journal of Pediatrics, 1983
- A RAPID BANDING TECHNIQUE FOR HUMAN CHROMOSOMESThe Lancet, 1971