These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
190 related items for PubMed ID: 4777947
1. The differentiation of the nature of the segregation of inheritance in the analysis of complete genealogical data. Sirotkin VM, Pazoni I, Farzan RKh. Sov Genet; 1973 Nov 15; 7(7):940-7. PubMed ID: 4777947 [No Abstract] [Full Text] [Related]
2. [Pedigree study of pathological myopia]. Yu ZQ, Fu CW, Shen FM, Chu RY. Yi Chuan Xue Bao; 2005 Feb 15; 32(2):130-5. PubMed ID: 15759859 [Abstract] [Full Text] [Related]
3. Genetic analysis of the inheritance of otosclerosis. Gapanavichyus BM, Venslauskas MI. Sov Genet; 1974 Apr 01; 8(2):251-60. PubMed ID: 4846192 [No Abstract] [Full Text] [Related]
4. [Genealogical analysis of dominant mutation in neurofibromatosis (Recklinghausen's disease)]. Sergeev AS. Genetika; 1973 Nov 01; 9(11):153-8. PubMed ID: 4219927 [No Abstract] [Full Text] [Related]
5. The ENCU scoring system. A strategy for solving a class of single-locus genetic counseling problems. Chase GA, Murphy EA, Bolling DR. Clin Genet; 1971 Nov 01; 2(3):141-8. PubMed ID: 5111757 [No Abstract] [Full Text] [Related]
6. Genetic analysis of cleft lip with or without cleft palate in Danish kindreds. Marazita ML, Spence MA, Melnick M. Am J Med Genet; 1984 Sep 01; 19(1):9-18. PubMed ID: 6496575 [Abstract] [Full Text] [Related]
7. [Dermatologic problems in population genetics]. Kozłowski J, Sitniewski S. Przegl Dermatol; 1975 Sep 01; 62(2):265-70. PubMed ID: 1096239 [No Abstract] [Full Text] [Related]
8. Genetic studies of familial amyloid polyneuropathy in the Arao district of Japan: I. The genealogical survey. Sakoda S, Suzuki T, Higa S, Ueji M, Kishimoto S, Hayashi A, Yasuda N, Takaba Y, Nakajima A. Clin Genet; 1983 Nov 01; 24(5):334-8. PubMed ID: 6580980 [Abstract] [Full Text] [Related]
9. Dominant and recessive inheritance of morbid obesity associated with melanocortin 4 receptor deficiency. Farooqi IS, Yeo GS, Keogh JM, Aminian S, Jebb SA, Butler G, Cheetham T, O'Rahilly S. J Clin Invest; 2000 Jul 01; 106(2):271-9. PubMed ID: 10903343 [Abstract] [Full Text] [Related]
10. [Genetic analysis of the Ehlers-Danlos syndrome in a large family tree]. Prytkov AN, Kozlova SI, Sultanova FA, Blinnikova OE, Gar'kavtsev IV. Genetika; 1984 May 01; 20(5):868-73. PubMed ID: 6234198 [Abstract] [Full Text] [Related]
11. A background to human and medical genetics. Rickard BJ. Guys Hosp Rep; 1967 May 01; 116(3):207-44. PubMed ID: 4871727 [No Abstract] [Full Text] [Related]
12. Sexual dimorphism and polygenic inheritance in man. Nurse GT. S Afr J Med Sci; 1974 May 01; 39(2):91-7. PubMed ID: 4450159 [No Abstract] [Full Text] [Related]