Grundfast KM - Search Results

1

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.

2

Further elucidation of the genomic structure of PAX3, and identification of two different point mutations within the PAX3 homeobox that cause Waardenburg syndrome type 1 in two families.

Lalwani AK, Brister JR, Fex J, Grundfast KM, Ploplis B, San Agustin TB, Wilcox ER. Lalwani AK, et al. Among authors: grundfast km. Am J Hum Genet. 1995 Jan;56(1):75-83. Am J Hum Genet. 1995. PMID: 7825605 Free PMC article.

3

A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2.

Lalwani AK, Brister JR, Fex J, Grundfast KM, Pikus AT, Ploplis B, San Agustin T, Skarka H, Wilcox ER. Lalwani AK, et al. Among authors: grundfast km. Am J Hum Genet. 1994 Oct;55(4):685-94. Am J Hum Genet. 1994. PMID: 7942846 Free PMC article.

4

Genetics and molecular biology of deafness.

Grundfast KM, Atwood JL, Chuong D. Grundfast KM, et al. Otolaryngol Clin North Am. 1999 Dec;32(6):1067-88. doi: 10.1016/s0030-6665(05)70195-x. Otolaryngol Clin North Am. 1999. PMID: 10523453 Free article. Review.

5

Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28.

Peters LM, Anderson DW, Griffith AJ, Grundfast KM, San Agustin TB, Madeo AC, Friedman TB, Morell RJ. Peters LM, et al. Among authors: grundfast km. Hum Mol Genet. 2002 Nov 1;11(23):2877-85. doi: 10.1093/hmg/11.23.2877. Hum Mol Genet. 2002. PMID: 12393799

6

Vocal cord paralysis.

Grundfast KM, Harley E. Grundfast KM, et al. Otolaryngol Clin North Am. 1989 Jun;22(3):569-97. Otolaryngol Clin North Am. 1989. PMID: 2657584 Review.

7

Ethical and cultural considerations in research on hereditary deafness.

Grundfast KM, Rosen J. Grundfast KM, et al. Otolaryngol Clin North Am. 1992 Oct;25(5):973-8. Otolaryngol Clin North Am. 1992. PMID: 1408199 No abstract available.

8

Making a Major Change: Changing Your Practice Setting, Retirement, and Locums.

Hesham HT, Grundfast K, Sarber K. Hesham HT, et al. Otolaryngol Clin North Am. 2022 Feb;55(1):33-41. doi: 10.1016/j.otc.2021.08.010. Otolaryngol Clin North Am. 2022. PMID: 34823719 Review.

9

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. Among authors: grundfast km. Am J Hum Genet. 1994 Oct;55(4):728-37. Am J Hum Genet. 1994. PMID: 7942851 Free PMC article.

10

Otologic manifestations of Wolf-Hirschhorn syndrome.

Lesperance MM, Grundfast KM, Rosenbaum KN. Lesperance MM, et al. Among authors: grundfast km. Arch Otolaryngol Head Neck Surg. 1998 Feb;124(2):193-6. doi: 10.1001/archotol.124.2.193. Arch Otolaryngol Head Neck Surg. 1998. PMID: 9485112

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