Found: 8
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King Tutankhamun's Family and Demise.
- Published in:
- 2010
- By:
- Publication type:
- Letter
Ancestry and Pathology in King Tutankhamun's Family.
- Published in:
- JAMA: Journal of the American Medical Association, 2010, v. 303, n. 7, p. 638, doi. 10.1001/jama.2010.121
- By:
- Publication type:
- Article
Familial Leydig Cell Hypoplasia as a Cause of Male Pseudohermaphroditism.
- Published in:
- Human Heredity, 1987, v. 37, n. 1, p. 36, doi. 10.1159/000153675
- By:
- Publication type:
- Article
Molecular analysis of 5α-reductase type 2 gene in eight unrelated egyptian children with suspected 5α-reductase deficiency: prevalence of the G34R mutation.
- Published in:
- Clinical Endocrinology, 2003, v. 58, n. 5, p. 627, doi. 10.1046/j.1365-2265.2003.01763.x
- By:
- Publication type:
- Article
Developing a Road Map to Spread Genomic Knowledge in Africa: 10th Conference of the African Society of Human Genetics, Cairo, Egypt.
- Published in:
- American Journal of Tropical Medicine & Hygiene, 2020, v. 102, n. 4, p. 719, doi. 10.4269/ajtmh.19-0408
- By:
- Publication type:
- Article
Schistosoma hematobium soluble egg antigens induce proliferation of urothelial and endothelial cells.
- Published in:
- World Journal of Urology, 2001, v. 19, n. 4, p. 263, doi. 10.1007/s003450100217
- By:
- Publication type:
- Article
Insights from ancient DNA analysis of Egyptian human mummies: clues to disease and kinship.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. R1, p. R24, doi. 10.1093/hmg/ddaa223
- By:
- Publication type:
- Article
Mutational spectrum of NF1 gene in 24 unrelated Egyptian families with neurofibromatosis type 1.
- Published in:
- Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 12, p. 1, doi. 10.1002/mgg3.1631
- By:
- Publication type:
- Article