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

. 1951 Sep;3(3):254-66.

Some statistical problems posed by Waardenburg's data on dystopia canthorum and associated anomalies

PMID: 14902765
PMCID: PMC1716406

Some statistical problems posed by Waardenburg's data on dystopia canthorum and associated anomalies

C W COTTERMAN. Am J Hum Genet. 1951 Sep.

. 1951 Sep;3(3):254-66.

Author

PMID: 14902765
PMCID: PMC1716406

No abstract available

PubMed Disclaimer

Similar articles

Heterogeneity in Waardenburg syndrome.
Hageman MJ, Delleman JW. Hageman MJ, et al. Am J Hum Genet. 1977 Sep;29(5):468-85. Am J Hum Genet. 1977. PMID: 331943 Free PMC article. Review.
Pigment distribution in Waardenburg's syndrome: a new hypothesis.
Nork TM, Shihab ZM, Young RS, Price J. Nork TM, et al. Graefes Arch Clin Exp Ophthalmol. 1986;224(6):487-92. doi: 10.1007/BF02154734. Graefes Arch Clin Exp Ophthalmol. 1986. PMID: 3792843
Apparent non-penetrance for dystopia in Waardenburg syndrome type I, with some hints on the diagnosis of dystopia canthorum.
Arias S, Mota M. Arias S, et al. J Genet Hum. 1978 Jun;26(2):103-31. J Genet Hum. 1978. PMID: 670940
Audiometric findings in 34 patients with Waardenburg's syndrome.
Hageman MJ. Hageman MJ. J Laryngol Otol. 1977 Jul;91(7):575-84. doi: 10.1017/s0022215100084073. J Laryngol Otol. 1977. PMID: 408454
Finding the gene(s) for Waardenburg syndrome(s).
Grundfast KM, San Agustin TB. Grundfast KM, et al. Otolaryngol Clin North Am. 1992 Oct;25(5):935-51. Otolaryngol Clin North Am. 1992. PMID: 1408197 Review.

See all similar articles

Cited by

Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium.
Farrer LA, Grundfast KM, Amos J, Arnos KS, Asher JH Jr, Beighton P, Diehl SR, Fex J, Foy C, Friedman TB, et al. Farrer LA, et al. Am J Hum Genet. 1992 May;50(5):902-13. Am J Hum Genet. 1992. PMID: 1349198 Free PMC article.
Heterogeneity in Waardenburg syndrome.
Hageman MJ, Delleman JW. Hageman MJ, et al. Am J Hum Genet. 1977 Sep;29(5):468-85. Am J Hum Genet. 1977. PMID: 331943 Free PMC article. Review.
A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness.
WAARDENBURG PJ. WAARDENBURG PJ. Am J Hum Genet. 1951 Sep;3(3):195-253. Am J Hum Genet. 1951. PMID: 14902764 Free PMC article. No abstract available.
WAARDENBURG'S SYNDROME: REPORT OF A PEDIGREE.
HANSEN AC, ACKAOUY G, CRUMP EP. HANSEN AC, et al. J Natl Med Assoc. 1965 Jan;57(1):8-12. J Natl Med Assoc. 1965. PMID: 14269024 Free PMC article. No abstract available.
Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypes.
Farrer LA, Arnos KS, Asher JH Jr, Baldwin CT, Diehl SR, Friedman TB, Greenberg J, Grundfast KM, Hoth C, Lalwani AK, et al. Farrer LA, et al. Am J Hum Genet. 1994 Oct;55(4):728-37. Am J Hum Genet. 1994. PMID: 7942851 Free PMC article.

References

1. Am J Hum Genet. 1951 Sep;3(3):195-253 - PubMed

MeSH terms

Actions
Actions
Actions

LinkOut - more resources

Full Text Sources
- Europe PubMed Central
- PubMed Central