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New recessive syndrome characterized by increased chromosomal breakage and several findings which overlap with Fanconi anemia

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Year: 1998
Type: article
Study design: Case Report
Source: American Journal of Medical Genetics
DOI: 10.1002/(sici)1096-8628(19980616)78:1<70::aid-ajmg15>3.0.co;2-l
Authors: Philip F. Giampietro, Arleen D. Auerbach, Ellen R. Elias, Alyson Gutman, Nancy J. Zellers, Jessica G. Davis
Institutions: Lincoln Medical Center, Cornell University, Rockefeller University, Boston Children's Hospital
Language: English

Topic: DNA Repair Mechanisms
Subfield: Molecular Biology
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, National Heart, Lung, and Blood Institute, National Center for Research Resources, NIH Clinical Center
Awards: GENERAL CLINICAL RESEARCH CENTER, G3460795981, G367656647
OpenAlex ID: W2133553852
FWCI: 0.465
Cites: 23
Cited by: 8
Related to: 10
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