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Academic Journal

Endocrine profiling in patients with Fanconi anemia, homozygous for a FANCG founder mutation.

  • Authors : Dillon B; Division of Human Genetics, National Health Laboratory Service and School of Pathology, Faculty of Health Sciences, The University of the Witwatersrand, Johannesburg, Gauteng, South Africa.; Feben C

Subjects: Mutation*; Fanconi Anemia/Fanconi Anemia/Fanconi Anemia/*genetics ; Fanconi Anemia Complementation Group G Protein/Fanconi Anemia Complementation Group G Protein/Fanconi Anemia Complementation Group G Protein/*genetics

  • Source: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2020 Aug; Vol. 8 (8), pp. e1351. Date of Electronic Publication: 2020 Jun 11.Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 101603758 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Fahr's syndrome presenting as seizures during pregnancy – A case report.

Subjects: *SEIZURES (Medicine); *SYNDROMES; *PREGNANCY

  • Source: Journal of Obstetric Anaesthesia & Critical Care. Jul-Dec2020, Vol. 10 Issue 2, p140-142. 3p.

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  • 1-10 ل  56 نتائج ل ""Endocrine abnormalities""