Skip to main content
PMC home page
American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 1973 May;25(3):237–246.

The incidence of genetic disease in a University hospital population.

N Day, L B Holmes
PMCID: PMC1762539  PMID: 4704856

Full text

PDF
241

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Brown W. T., Puranik S. R., Altman D. H., Hardin H. C., Jr Wilms' tumor in three successive generations. Surgery. 1972 Nov;72(5):756–761. [PubMed] [Google Scholar]
  2. Burger R. H. A theory on the nature of transmission of congenital vesicoureteral reflux. J Urol. 1972 Aug;108(2):249–254. doi: 10.1016/s0022-5347(17)60702-x. [DOI] [PubMed] [Google Scholar]
  3. CARTER C. O. Changing patterns in the causes of death at the Hospital for Sick Children. Great Ormond St J. 1956;(11):65–68. [PubMed] [Google Scholar]
  4. Carter C. O. Genetics of common disorders. Br Med Bull. 1969 Jan;25(1):52–57. doi: 10.1093/oxfordjournals.bmb.a070671. [DOI] [PubMed] [Google Scholar]
  5. DeMeyer W. Megalencephaly in children. Clinical syndromes, genetic patterns, and differential diagnosis from other causes of megalocephaly. Neurology. 1972 Jun;22(6):634–643. doi: 10.1212/wnl.22.6.634. [DOI] [PubMed] [Google Scholar]
  6. Lang D. J. The association of indirect inguinal hernia with congenital cytomegalic inclusion disease. Pediatrics. 1966 Nov;38(5):913–916. [PubMed] [Google Scholar]
  7. Lanzkowsky P., Colussi P., McKenzie D. Pelger-Huët anomaly of the granulocytes in a Cape colored family. J Pediatr. 1965 Nov;67(5):826–832. doi: 10.1016/s0022-3476(65)80373-0. [DOI] [PubMed] [Google Scholar]
  8. Leonard C. O., Chase G. A., Childs B. Genetic counseling: a consumers' view. N Engl J Med. 1972 Aug 31;287(9):433–439. doi: 10.1056/NEJM197208312870904. [DOI] [PubMed] [Google Scholar]
  9. Lubs M. L. Emperic risks for genetic counseling in families with allergy. J Pediatr. 1972 Jan;80(1):26–31. doi: 10.1016/s0022-3476(72)80448-7. [DOI] [PubMed] [Google Scholar]
  10. Passarge E. The genetics of Hirschsprung's disease. Evidence for heterogeneous etiology and a study of sixty-three families. N Engl J Med. 1967 Jan 19;276(3):138–143. doi: 10.1056/NEJM196701192760303. [DOI] [PubMed] [Google Scholar]
  11. Reiss J. A., Menashe V. D. Genetic counseling and congenital heart disease. J Pediatr. 1972 Apr;80(4):655–656. doi: 10.1016/s0022-3476(72)80069-6. [DOI] [PubMed] [Google Scholar]
  12. Rimoin D. L. Inheritance in diabetes mellitus. Med Clin North Am. 1971 Jul;55(4):807–819. doi: 10.1016/s0025-7125(16)32477-4. [DOI] [PubMed] [Google Scholar]
  13. Roberts D. F., Chavez J., Court S. D. The genetic component in child mortality. Arch Dis Child. 1970 Feb;45(239):33–38. doi: 10.1136/adc.45.239.33. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Sibinga M. S., Friedman C. J. Complexities of parental understanding of phenylketonuria. Pediatrics. 1971 Aug;48(2):216–224. [PubMed] [Google Scholar]
  15. Smith D. W., Aase J. M. Polygenic inheritance of certain common malformations. Evidence and empiric recurrence risk data. J Pediatr. 1970 May;76(5):652–659. doi: 10.1016/s0022-3476(70)80282-7. [DOI] [PubMed] [Google Scholar]
  16. Watson W., Cann H. M., Farber E. M., Nall M. L. The genetics of psoriasis. Arch Dermatol. 1972 Feb;105(2):197–207. [PubMed] [Google Scholar]

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

RESOURCES