This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features!

Skip to main page content

Add to Collections

Your saved search

Name of saved search:

Search terms:

Test search terms

Would you like email updates of new search results?

Yes
No

Email: (change)

Frequency:

Which day?

Which day?

Report format:

Send at most:

Send even when there aren't any new results

Optional text in email:

Your RSS Feed

. 1970 Nov;22(6):630-44.

Family studies of early childhood deafness ascertained through the Clarke School for the Deaf

C S Chung, K S Brown

PMID: 5518458
PMCID: PMC1706664

Family studies of early childhood deafness ascertained through the Clarke School for the Deaf

C S Chung et al. Am J Hum Genet. 1970 Nov.

. 1970 Nov;22(6):630-44.

Authors

C S Chung, K S Brown

PMID: 5518458
PMCID: PMC1706664

No abstract available

PubMed Disclaimer

Similar articles

[The statistical inclusion of exogenous cases in simple recessive heredity with application to recessive deaf-mutism].
Rosin S. Rosin S. Arch Julius Klaus Stift Vererbungsforsch Sozialanthropol Rassenhyg. 1963;38(3-4):253-62. Arch Julius Klaus Stift Vererbungsforsch Sozialanthropol Rassenhyg. 1963. PMID: 5899907 German. No abstract available.
[The lack of recessive deaf-mutes in affected siblings].
Pfädler U. Pfädler U. Arch Julius Klaus Stift Vererbungsforsch Sozialanthropol Rassenhyg. 1963;38(3-4):262-72. Arch Julius Klaus Stift Vererbungsforsch Sozialanthropol Rassenhyg. 1963. PMID: 5899908 French. No abstract available.
Genetic epidemiological studies of early-onset deafness in the U.S. school-age population.
Marazita ML, Ploughman LM, Rawlings B, Remington E, Arnos KS, Nance WE. Marazita ML, et al. Am J Med Genet. 1993 Jun 15;46(5):486-91. doi: 10.1002/ajmg.1320460504. Am J Med Genet. 1993. PMID: 8322805
Nonsyndromal profound genetic deafness in childhood.
Cremers CW, Marres HA, van Rijn PM. Cremers CW, et al. Ann N Y Acad Sci. 1991;630:191-6. doi: 10.1111/j.1749-6632.1991.tb19587.x. Ann N Y Acad Sci. 1991. PMID: 1952589 Review.
Genetics of deafness: recent advances and clinical implications.
Goldfarb A, Avraham KB. Goldfarb A, et al. J Basic Clin Physiol Pharmacol. 2002;13(2):75-88. doi: 10.1515/jbcpp.2002.13.2.75. J Basic Clin Physiol Pharmacol. 2002. PMID: 16411422 Review.

See all similar articles

Cited by

On the genetics of prelingual deafness.
Majumder PP, Ramesh A, Chinnappan D. Majumder PP, et al. Am J Hum Genet. 1989 Jan;44(1):86-99. Am J Hum Genet. 1989. PMID: 2909169 Free PMC article.
Sensorineural deafness inherited as a tissue specific mitochondrial disorder.
Jaber L, Shohat M, Bu X, Fischel-Ghodsian N, Yang HY, Wang SJ, Rotter JI. Jaber L, et al. J Med Genet. 1992 Feb;29(2):86-90. doi: 10.1136/jmg.29.2.86. J Med Genet. 1992. PMID: 1613771 Free PMC article.
Responsibilities in genetic counseling for the deaf.
Boughman JA, Shaver KA. Boughman JA, et al. Am J Hum Genet. 1983 Nov;35(6):1317-9. Am J Hum Genet. 1983. PMID: 6650507 Free PMC article. No abstract available.
Consanguinity analysis of congenital deafness in Northern Israel.
Costeff H, Dar H. Costeff H, et al. Am J Hum Genet. 1980 Jan;32(1):64-8. Am J Hum Genet. 1980. PMID: 7361765 Free PMC article.
Nonsyndromic hearing impairment: unparalleled heterogeneity.
Van Camp G, Willems PJ, Smith RJ. Van Camp G, et al. Am J Hum Genet. 1997 Apr;60(4):758-64. Am J Hum Genet. 1997. PMID: 9106521 Free PMC article. Review. No abstract available.

See all "Cited by" articles

References

1. Eugen Q. 1968 Mar;15(1):22-33 - PubMed
1. J Otolaryngol Soc Aust. 1968 Mar;2(3):25-33 - PubMed
1. Med Clin North Am. 1969 Jul;53(4):741-72 - PubMed
1. Ann Hum Genet. 1958 Feb;22(2):153-7 - PubMed
1. Am J Hum Genet. 1959 Mar;11(1):1-16 - PubMed

MeSH terms

Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions

LinkOut - more resources

Full Text Sources
- Europe PubMed Central
- PubMed Central