Found: 13
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Connexin 26 Gene Mutations in Non-Syndromic Hearing Loss Among Kuwaiti Patients.
- Published in:
- Medical Principles & Practice, 2013, v. 23, n. 1, p. 74, doi. 10.1159/000348304
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- Article
Mutation and Linkage Analysis in Genetic Counseling for Phenylketonuria in Kuwait.
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- Medical Principles & Practice, 1999, v. 8, n. 3, p. 217, doi. 10.1159/000026095
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- Article
Molecular Analysis of the G6PD-Mediterranean Mutation in Kuwait.
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- Medical Principles & Practice, 1998, v. 7, n. 3, p. 209, doi. 10.1159/000026044
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- Article
Complete Testicular Feminization Syndrome with 47, XYY Karyotype: A Double Hit Phenomenon.
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- Medical Principles & Practice, 1997, v. 6, n. 4, p. 216, doi. 10.1159/000157555
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- Article
A Kuwaiti Patient with Osteopetrosis, Renal Tubular Acidosis and Cerebral Calcification is Homozygous for a Splice Junction Mutation in the Carbonic Anhydrase Gene.
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- Medical Principles & Practice, 1996, v. 5, n. 4, p. 234, doi. 10.1159/000157412
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- Article
Alzheimer’s disease in adults with Down syndrome.
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- Middle East Journal of Medical Genetics, 2013, v. 2, n. 1, p. 1, doi. 10.1097/01.MXE.0000422778.05483.9e
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- Article
Poland Syndrome and Associated Dextrocardia in Kuwait.
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- Medical Principles & Practice, 1994, v. 4, n. 3, p. 121, doi. 10.1159/000157500
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- Article
Molecular Mechanisms of Non-Mendelian Inheritance in Genetic Diseases.
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- Medical Principles & Practice, 1994, v. 4, n. 1, p. 1, doi. 10.1159/000157481
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- Article
Population Study of Common Glucose-6-Phosphate Dehydrogenase Mutations in Kuwait.
- Published in:
- Human Heredity, 1999, v. 49, n. 1, p. 41, doi. 10.1159/000022838
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- Article
Macrosomia, microphthalmia, ± cleft palate and early infant death: a new autosomal recessive syndrome.
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- Clinical Genetics, 1989, v. 36, n. 3, p. 174, doi. 10.1111/j.1399-0004.1989.tb03184.x
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- Article
Trisomy 18 clustering in Kuwait.
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- Clinical Genetics, 1987, v. 32, n. 6, p. 379, doi. 10.1111/j.1399-0004.1987.tb03153.x
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- Article
Hereditary multiple exostoses, macrocephaly, congenital heart disease, developmental delay, and mental retardation in a female patient: A possible new syndrome? Or new association?
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- Egyptian Journal of Medical Human Genetics, 2011, v. 12, n. 1, p. 95, doi. 10.1016/j.ejmhg.2011.02.006
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- Article
Trisomy 9 syndrome in a neonate with unusual features.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2009, v. 10, n. 2, p. 238
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- Article