Chotai KA[au] - Search Results

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Year	Number of Results
1978	1
1992	2
1994	1
1998	1
2023	0

Page 1

Six cases of 7p deletion: clinical, cytogenetic, and molecular studies.

Chotai KA, Brueton LA, van Herwerden L, Garrett C, Hinkel GK, Schinzel A, Mueller RF, Speleman F, Winter RM. Chotai KA, et al. Am J Med Genet. 1994 Jul 1;51(3):270-6. doi: 10.1002/ajmg.1320510320. Am J Med Genet. 1994. PMID: 7521123 Review.

A rapid, PCR based test for differential molecular diagnosis of Prader-Willi and Angelman syndromes.

Chotai KA, Payne SJ. Chotai KA, et al. J Med Genet. 1998 Jun;35(6):472-5. doi: 10.1136/jmg.35.6.472. J Med Genet. 1998. PMID: 9643288 Free PMC article.

The acrocallosal syndrome and Greig syndrome are not allelic disorders.

Brueton LA, Chotai KA, van Herwerden L, Schinzel A, Winter RM. Brueton LA, et al. Among authors: chotai ka. J Med Genet. 1992 Sep;29(9):635-7. doi: 10.1136/jmg.29.9.635. J Med Genet. 1992. PMID: 1404293 Free PMC article.

The mapping of a gene for craniosynostosis: evidence for linkage of the Saethre-Chotzen syndrome to distal chromosome 7p.

Brueton LA, van Herwerden L, Chotai KA, Winter RM. Brueton LA, et al. Among authors: chotai ka. J Med Genet. 1992 Oct;29(10):681-5. doi: 10.1136/jmg.29.10.681. J Med Genet. 1992. PMID: 1433226 Free PMC article.

Evidence that the mutant enzyme in fibroblasts of a patient with mannosidosis does not crossreact with antiserum raised against normal acidic alpha-D-mannosidase.

Burditt LJ, Chotai KA, Winchester BG. Burditt LJ, et al. Among authors: chotai ka. FEBS Lett. 1978 Jul 15;91(2):186-9. doi: 10.1016/0014-5793(78)81168-5. FEBS Lett. 1978. PMID: 98350 Free article. No abstract available.

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