Поисковый запрос: (<.>S=ТИП НАСЛЕДОВАНИЯ<.>) |
Общее количество найденных документов : 43
Показаны документы с 1 по 20
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1.
| A mendelian form of obsessive-compulsive disorder derived from symptom-based factors // Amer. J. Med. Genet., 1998. Vol. 81, N 6.-С.546
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2.
| A new platelet-specific antigen, Nak{a}, involved in the refractoriness of HLA-matched platelet transfusion // Vox sang, 1989. Vol. 57, N 3.-С.213-217
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3.
| Adhami J.E. La maladie de Wilson en Albanie // Med. et chir. dig., 1996. Vol. 25, N 3.-С.145
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| Autosomal dominant polycystisk nyresygdom hos perserkat // Dan. veterinaertidsskr., 1998. Vol. 81, N 16.-С.585-588
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| Balci Diastematomyelia in two sisters // Amer. J. Med. Genet., 1999. Vol. 86, N 2.-С.180-182
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| Bravo-Luna M. Tachycardia: An autosomal, monogenic, biallelic, recessive trait // Med. Hypotheses, 2000. Vol. 54, N 2.-С.307-309
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| Cacheux Le syndrome de Waardenburg // C. r. seances Soc. biol., 1996. Vol. 190, N 5-6.-С.577-580
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| Complex segregation analysis of obsessive-compulsive disorder in 141 families of eating disorder probands, with and without obsessive-compulsive disorder // Amer. J. Med. Genet., 2000. Vol. 96, N 3.-С.384-391
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| Couzigou P. Genetique et risque alcoolique // Sem. Hop. Paris, 1990. Vol. 66, N 37-38.-С.2151-2154
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| Drigalenko E. Segregation analysis of late onset Alzheimer's disease: Evidence for a major gene // Genet. Epidemiol., 1999. Vol. 17, N 3.-С.208
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| Evidence for further breast cancer susceptibility genes in addition to BRCA1 and BRCA2: The ABC study // Genet. Epidemiol., 1999. Vol. 17, N 3.-С.197
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12.
| Familial temporal lobe epilepsy. Autosomal dominant inheritance in a large pedigree from Southern Italy // Epilepsy Res., 2000. Vol. 38, N 2-3.-С.127-132
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| Family with low-grade neuroendocrine carcinoma of salivary glands, severe sensorineural hearing loss, and enamel hypoplasia // Amer. J. Med. Genet., 1999. Vol. 83, N 3.-С.183-186
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14.
| Gusmano Nephronophthisis-medullary cystic disease: Clinical and genetic aspects // J. Nephrol., 1998. Vol. 11, N 5.-С.224-228
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| Gusmano Nephronophthisis-medullary cystic disease: Clinical and genetic aspects // J. Nephrol., 1998. Vol. 11, N 5.-С.224-228
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16.
| Happle Poland anomaly may be explained as a paradominant trait // Amer. J. Med. Genet., 1999. Vol. 87, N 4.-С.364-365
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| Ichthyosis congenita Type II // H+G, 1999. Vol. 74, N 4.-С.223-225
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18.
| Ichthyosis congenita Type II // H+G, 1999. Vol. 74, N 4.-С.223-225
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19.
| Inheritance of Niikawa-Kuroki (Kabuki makeup) syndrome // Amer. J. Med. Genet., 1996. Vol. 66, N 3.-С.368
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20.
| Inheritance of T helper immunodeficiency (thid) in LEC mutant rats // Immunogenetics, 1991. Vol. 33, N 3.-С.216-219
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