International Fanconi Anemia Registry: First Report
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Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-74179-1_1.pdf
Reference24 articles.
1. Alter BP, Potter NU (1983) Long term outcome in Fanconi’s anemia: description of 26 cases and review of the literature. In: German J (ed) Chromosome mutation and neoplasia. Liss, New York, pp 43–62
2. Auerbach AD, Wolman SR (1976) Susceptibility of Fanconi’s anaemia fibroblasts to chromosome damage by carcinogens. Nature 261: 494–496
3. Auerbach AD, Wolman SR (1978) Carcinogen-induced chromosome breakage in Fanconi’s anaemia heterozygous cells. Nature 271: 69–71
4. Auerbach AD, Adler B, Chaganti RSK (1981) Prenatal and postnatal diagnosis and carrier detection of Fanconi anemia by a cytogenetic method. Pediatrics 67: 128–135
5. Auerbach AD, Sagi M, Adler B (1985) Fanconi anemia: prenatal diagnosis in 30 fetuses at risk. Pediatrics 76: 794–800
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1. Detection of somatic mosaicism and classification of Fanconi anemia patients by analysis of the FA/BRCA pathway;Blood;2005-02-01
2. Spontaneous Chromosome Aberrations in Fanconi's Anemia Patients are Located at Fragile Sites and Acute Myeloid Leukemia Breakpoints;Hereditas;2004-05-28
3. VACTERL with hydrocephalus in twins due to Fanconi anemia (FA): Mutation in the FAC gene;American Journal of Medical Genetics;1997-01-10
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5. Absent thumb, immune disorder, and congenital anemia presenting with hydrops fetalis;American Journal of Medical Genetics;1992-03-01
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