Found: 6
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Genotype phenotype correlations for hearing impairment: Approaches to management.
- Published in:
- Clinical Genetics, 2014, v. 85, n. 6, p. 514, doi. 10.1111/cge.12339
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- Publication type:
- Article
Screening male intracytoplasmic sperm injection candidates for mutations of the follicle stimulating hormone receptor gene.
- Published in:
- 1998
- By:
- Publication type:
- journal article
Microdeletions of the Y chromosome and intracytoplasmic sperm injection: from gene to clinic.
- Published in:
- Human Reproduction, 1997, v. 12, n. 4, p. 687, doi. 10.1093/humrep/12.4.687
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- Publication type:
- Article
Mutations in CHD7 in patients with CHARGE syndrome cause T–B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndrome.
- Published in:
- Clinical & Experimental Immunology, 2008, v. 153, n. 1, p. 75, doi. 10.1111/j.1365-2249.2008.03681.x
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- Publication type:
- Article
Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis.
- Published in:
- Clinical Genetics, 2011, v. 79, n. 1, p. 49, doi. 10.1111/j.1399-0004.2010.01486.x
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- Publication type:
- Article
CHD7 mutations in patients initially diagnosed with Kallmann syndrome – the clinical overlap with CHARGE syndrome.
- Published in:
- Clinical Genetics, 2009, v. 75, n. 1, p. 65, doi. 10.1111/j.1399-0004.2008.01107.x
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- Publication type:
- Article