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.
87 related articles for article (PubMed ID: 7172146)
1. [Genetic epidemiology, foundation of true prevention: approach and results]. Philippe P Can J Public Health; 1982; 73(5):350-7. PubMed ID: 7172146 [No Abstract] [Full Text] [Related]
3. Current concepts in genetics. Principles of medical genetics (first of two parts). Erbe RW N Engl J Med; 1976 Feb; 294(7):381. PubMed ID: 1246290 [No Abstract] [Full Text] [Related]
4. Evolving methods in genetic epidemiology. I. Analysis of genetic and environmental factors in family studies. Beaty TH Epidemiol Rev; 1997; 19(1):14-23. PubMed ID: 9360898 [No Abstract] [Full Text] [Related]
5. [Hereditary chromosomal mosaicism and its importance for the affected family]. Zdansky R; Madl W; Rett A; Piperger A Wien Med Wochenschr; 1971 Jan; 121(4):59-63. PubMed ID: 4252342 [No Abstract] [Full Text] [Related]
6. The basics of genetic disease. Daniel WL Compr Ther; 1992 Apr; 18(4):6-12. PubMed ID: 1628484 [TBL] [Abstract][Full Text] [Related]
7. [Ecological changes and human heredity]. Bochkov NP; Katosova LD; Titenko NV; Filippova TV Klin Med (Mosk); 1990 May; 68(5):25-32. PubMed ID: 2204758 [No Abstract] [Full Text] [Related]
8. [Causes of hereditary diseases and the possibility of their perinatal diagnosis]. Brusilovskiĭ AI Akush Ginekol (Mosk); 1976 Dec; (12):62-4. PubMed ID: 828459 [No Abstract] [Full Text] [Related]
9. The susceptibility of the fetus and child to chemical pollutants. Monitoring for human mutagenesis. Sutton HE Pediatrics; 1974 May; 53(5):800-7. PubMed ID: 4416527 [No Abstract] [Full Text] [Related]
10. A family of severe congenital neutropenia with -199C to A substitution in ELA2 promoter. Matsushita H; Asai S; Komiya S; Inoue H; Yabe H; Miyachi H Am J Hematol; 2006 Dec; 81(12):985-6. PubMed ID: 16795059 [No Abstract] [Full Text] [Related]
11. [Genomic imprinting and human pathology. 2]. Cirillo Silengo M; Lerone M; Guala A Pediatr Med Chir; 1995; 17(5):389-94. PubMed ID: 8684991 [TBL] [Abstract][Full Text] [Related]
12. Problems in genetic counseling. Harris R Proc R Soc Med; 1971 May; 64(5):490-1. PubMed ID: 5576907 [No Abstract] [Full Text] [Related]
13. [Medical-genetic counseling (basic principles and methods)]. Davidenkova EF; Butomo IV Klin Med (Mosk); 1978 Apr; 56(4):12-27. PubMed ID: 351283 [No Abstract] [Full Text] [Related]
14. The use of pedigree, sib-pair and association studies of common diseases for genetic mapping and epidemiology. Freimer N; Sabatti C Nat Genet; 2004 Oct; 36(10):1045-51. PubMed ID: 15454942 [TBL] [Abstract][Full Text] [Related]
16. [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]
17. [Mutation process in man]. Bochkov NP Vestn Akad Med Nauk SSSR; 1976; (7):47-53. PubMed ID: 829196 [No Abstract] [Full Text] [Related]
18. New mechanisms for genetic disease and nontraditional modes of inheritance. Langlois S; Lopez-Rangel E; Hall JG Adv Pediatr; 1995; 42():91-111. PubMed ID: 8540441 [No Abstract] [Full Text] [Related]
19. Save the males! Page DC Nat Genet; 1997 Sep; 17(1):3. PubMed ID: 9288083 [No Abstract] [Full Text] [Related]