Поисковый запрос: (<.>S=ДОМИНАНТНЫЙ<.>) |
Общее количество найденных документов : 116
Показаны документы с 1 по 20
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1.
| A cancer family syndrome in twenty-four kindreds // Cancer Res., 1988. Vol. 48, N 18.-С.5358-5362
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2.
| A novel mutation of the RP1 gene (Lys778ter) associated with autosomal dominant retinitis pigmentosa // Brit. J. Ophthalmol., 2002. Vol. 86, N 3.-С.328-332
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3.
| A novel RPGR gene mutation in a Chinese family with X-linked dominant retinitis pigmentosa // Zhonghua yixue yichuanxue zazhi, 2005. Vol. 22, N 4.-С.396-398
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4.
| Arechaederra Analisis de la herencia del retinoblastoma en 8 familias // Rev. cub. pediat., 1989. Vol. 61, N 1.-С.67-74
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5.
| Atrofodermia vermiculada: Descripcion de tres casos en una familia // Actas dermo-sifiliogr., 1995. Vol. 86, N 10.-С.527-529
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6.
| Autosomal dominant polycystic kidney disease (ADPKD) and intrahepatic biliary tract abnormalities (60 patients) // Eur. Radiol., 1999. Vol. 9, прил. N 1.-С.S282
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7.
| Autosomal dominant polycystic liver disease in a family without polycystic kidney disease associated with a novel missense protein kinase C substrate 80K-H mutation // World J. Gastroenterol., 2005. Vol. 11, N 48.-С.7690-7693
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| Autosomal-dominant chroic mucocutaneous candidiasis with STAT1-mutation can be complicated with chronic active hepatitis and hypothyroidism // J. Clin. Immunol., 2012. Vol. 32, N 6.-С.1213-1220
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| Backenroth Does type 2 diabetes mellitus delay renal failure in autosomal dominant polycystic kidney disease? // Renal Failure, 2002. Vol. 24, N 6.-С.803-813
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| Braun Metaphyseal dysplasia. A new autosomal dominant type in a large German kindred // Amer. J. Med. Genet., 2001. Vol. 101, N 1.-С.74-77
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11.
| Cardiac involvement in autosomal-dominant polycystic kidney disease: A hypertensive heart disease // Clin. Nephrol., 2001. Vol. 56, N 3.-С.211-220
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12.
| Caro A case of familial multiple polyposis: A case study // Radiographer, 1993. Vol. 40, N 4.-С.158-160
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13.
| Characteristics of the bovine dominant follicle on day 10 of estrous cycle // Reprod. Domest. Anim., 1999. Vol. 34, N 1.-С.21
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14.
| Characterization of immunoreactive IGF-I pattern during the peri-ovulatory period of the oestrous cycle of thoroughbred mares and its relation to other hormones // Reprod. Domest. Anim., 2012. Vol. 47, N 1.-С.151-156
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15.
| Class II human leukocyte antigen genes and T cell receptor polymorphisms in patients with rheumatoid arthritis // Amer. J. Med., 1988. Vol. 85, N 6А.-С.14-16
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16.
| Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafness // Brit. J. Ophthalmol., 1997. Vol. 81, N 3.-С.207-213
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17.
| Clinical assessment and molecular genetics of an autosomal dominant retinitis pigmentosa in a Bulgarian Roma family // Acta med. bulg., 2011. Vol. 38, N 2.-С.46-50
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18.
| Constantinidis J. The dominant form of the pigmentary orthochromatic leukodystrophy (POLD) // Clin. Neuropathol., 1992. Vol. 11, N 4.-С.223
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19.
| Cowlishaw G. Dominance rank and mating success in male primates // Anim. Behav., 1991. Vol. 41, N 6.-С.1045-1056
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20.
| Craniosynostosis associated with ocular and distal limb defects is very likely caused by mutations in a gene different from FGFR, TWIST, and MSX2 // Amer. J. Med. Genet., 2002. Vol. 113, N 2.-С.200-206
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