Found: 8
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Tetrasomy 9p Mosaicism Associated with a Normal Phenotype in Two Cases.
- Published in:
- Cytogenetic & Genome Research, 2012, v. 136, n. 4, p. 237, doi. 10.1159/000337520
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- Article
Letter to the Editor Genetic counseling of medullary breast cancer patients.
- Published in:
- 2004
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- Publication type:
- Letter
Short Report Refining the primary open-angle glaucoma GLC1C region on chromosome 3 by haplotype analysis.
- Published in:
- Clinical Genetics, 2004, v. 65, n. 1, p. 40, doi. 10.1111/j..2004.00182.x
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- Article
Prelingual Nonsyndromic Hearing Loss in Greece.
- Published in:
- ORL, 2002, v. 64, n. 5, p. 321, doi. 10.1159/000066088
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- Publication type:
- Article
Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in a Greek population of blood donors.
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- American Journal of Hematology, 1999, v. 61, n. 4, p. 265, doi. 10.1002/(SICI)1096-8652(199908)61:4<265::AID-AJH8>3.0.CO;2-#
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- Article
A novel deletion mutation in the ALOX12B gene in a Kurdish family with autosomal recessive congenital ichthyosis.
- Published in:
- Journal of the European Academy of Dermatology & Venereology, 2016, v. 30, n. 11, p. e144, doi. 10.1111/jdv.13457
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- Article
Mutation analysis of the GJB2 (connexin 26) gene by DGGE in Greek patients with sensorineural deafness.
- Published in:
- Human Mutation, 2000, v. 16, n. 1, p. 7, doi. 10.1002/1098-1004(200007)16:1<7::AID-HUMU2>3.0.CO;2-A
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- Publication type:
- Article
ECEL1 mutation causes fetal arthrogryposis multiplex congenita.
- Published in:
- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 4, p. 731, doi. 10.1002/ajmg.a.37018
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- Publication type:
- Article