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3. [Heredity in ophthalmology]. Delleman JW; Bleeker-Wagemakers EM; van Schooneveld MJ Ned Tijdschr Geneeskd; 1987 Dec; 131(49):2226-30. PubMed ID: 3696248 [No Abstract] [Full Text] [Related]
4. Mendelian inheritance of isolated nonsyndromic cleft palate. Rollnick BR; Kaye CI Am J Med Genet; 1986 Jul; 24(3):465-73. PubMed ID: 3728565 [TBL] [Abstract][Full Text] [Related]
5. Myotonia levior: contribution to the nosography. Siciliano G; Risaliti R; Vignocchi G; Rossi B Riv Neurol; 1988; 58(5):204-9. PubMed ID: 3231989 [TBL] [Abstract][Full Text] [Related]
6. Sexual dimorphism and polygenic inheritance in man. Nurse GT S Afr J Med Sci; 1974; 39(2):91-7. PubMed ID: 4450159 [No Abstract] [Full Text] [Related]
8. Familial recurrent intrahepatic cholestasis of pregnancy: a genetic study providing evidence for transmission of a sex-limited, dominant trait. Holzbach RT; Sivak DA; Braun WE Gastroenterology; 1983 Jul; 85(1):175-9. PubMed ID: 6852450 [TBL] [Abstract][Full Text] [Related]
9. [Regional characteristics of the incidence of hereditary pathology in Uzbekistan]. Gar'kavtseva RF; Ginter EK; Revazov AA Vestn Akad Med Nauk SSSR; 1984; (7):69-75. PubMed ID: 6236633 [No Abstract] [Full Text] [Related]
10. [Association of chronic tubulo-interstitial nephropathy and of tapeto-retinal degeneration. Genetic study]. Bois E; Royer P Arch Fr Pediatr; 1970 May; 27(5):471-81. PubMed ID: 5425823 [No Abstract] [Full Text] [Related]
11. Genetics. The land between Mendelian and multifactorial inheritance. Burghes AH; Vaessin HE; de La Chapelle A Science; 2001 Sep; 293(5538):2213-4. PubMed ID: 11567125 [No Abstract] [Full Text] [Related]
13. [Renal glycosuria: dominant or recessive autosome anomaly? Mode of hereditary transmission based on the analysis of a 3-generation family tree]. De Marchi S; Proto G; Jengo A; Collinassi P; Basile A Minerva Med; 1983 Feb; 74(7):301-6. PubMed ID: 6828258 [TBL] [Abstract][Full Text] [Related]
14. Chronic nonhemolytic unconjugated hyperbilirubinemia with glucuronyl transferase deficiency: evidence for genetic heterogeneity. Arias IM; Gartner LM; Cohen M; Ben-Ezzer J; Levi AJ Trans Assoc Am Physicians; 1968; 81():66-75. PubMed ID: 5729564 [No Abstract] [Full Text] [Related]
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17. [Expression of dominant and recessive genes in mammalian ontogeny]. Koniukhov BV; Nonchev SG Zh Obshch Biol; 1981; 42(3):325-34. PubMed ID: 6169230 [No Abstract] [Full Text] [Related]
18. [Diversity of hereditary pathology in the population of Marii El Republic and its differentiation with respect to gene frequencies for hereditary diseases]. Ginter EK; Mamedova RA; Kozlova SI; Galkina VA; Moshkina IS; Rudenskaia GE; Khlebnikova OV; Nurbaev SD; Balanovskaia EV; Rassanov VP Genetika; 1998 Jul; 34(7):963-72. PubMed ID: 9749338 [TBL] [Abstract][Full Text] [Related]
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