Skip to main content

. 1966 Mar;18(2):187–200.

Holt-Oram syndrome: clinical and genetic study of a large family.

J C Gall Jr, A M Stern, M M Cohen, M S Adams, R T Davidson

PMCID: PMC1706161 PMID: 5904863

187

Images in this article

Fig. 2
on p.190

Fig. 3
on p.191

Fig. 4
on p.193

Selected References

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

COHEN M. M., CASSADY G., HANNA B. L. A genetic study of hereditary renal dysfunction with associated nerve deafness. Am J Hum Genet. 1961 Dec;13:379–389. [PMC free article] [PubMed] [Google Scholar]
GRAHAM J. B. Hereditary chronic kidney disease: an alternative to partial sex-linkage in the Utah kindred. Am J Hum Genet. 1959 Dec;11:333–338. [PMC free article] [PubMed] [Google Scholar]
HOLMES L. B. CONGENITAL HEART DISEASE AND UPPER-EXTREMITY DEFORMITIES: A REPORT OF TWO FAMILIES. N Engl J Med. 1965 Mar 4;272:437–444. doi: 10.1056/NEJM196503042720901. [DOI] [PubMed] [Google Scholar]
HOLT M., ORAM S. Familial heart disease with skeletal malformations. Br Heart J. 1960 Apr;22:236–242. doi: 10.1136/hrt.22.2.236. [DOI] [PMC free article] [PubMed] [Google Scholar]
MOORHEAD P. S., NOWELL P. C., MELLMAN W. J., BATTIPS D. M., HUNGERFORD D. A. Chromosome preparations of leukocytes cultured from human peripheral blood. Exp Cell Res. 1960 Sep;20:613–616. doi: 10.1016/0014-4827(60)90138-5. [DOI] [PubMed] [Google Scholar]
PRUZANSKI W. FAMILIAL CONGENITAL MALFORMATIONS OF THE HEART AND UPPER LIMBS. A SYNDROME OF HOLT-ORAM. Cardiologia. 1964;45:21–38. doi: 10.1159/000168096. [DOI] [PubMed] [Google Scholar]
Shaw R. F., Glover R. A. Abnormal Segregation in Hereditary Renal Disease with Deafness. Am J Hum Genet. 1961 Mar;13(1 Pt 1):89–97. [PMC free article] [PubMed] [Google Scholar]

ACTIONS

PDF (2.2 MB)

RESOURCES