Walter MA - Search Results

1

Autosomal-dominant iridogoniodysgenesis and Axenfeld-Rieger syndrome are genetically distinct.

Walter MA, Mirzayans F, Mears AJ, Hickey K, Pearce WG. Walter MA, et al. Ophthalmology. 1996 Nov;103(11):1907-15. doi: 10.1016/s0161-6420(96)30408-9. Ophthalmology. 1996. PMID: 8942889

2

Mutation of the PAX6 gene in patients with autosomal dominant keratitis.

Mirzayans F, Pearce WG, MacDonald IM, Walter MA. Mirzayans F, et al. Among authors: walter ma. Am J Hum Genet. 1995 Sep;57(3):539-48. Am J Hum Genet. 1995. PMID: 7668281 Free PMC article.

3

Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25.

Mears AJ, Mirzayans F, Gould DB, Pearce WG, Walter MA. Mears AJ, et al. Among authors: walter ma. Am J Hum Genet. 1996 Dec;59(6):1321-7. Am J Hum Genet. 1996. PMID: 8940278 Free PMC article.

4

Identification of the human chromosomal region containing the iridogoniodysgenesis anomaly locus by genomic-mismatch scanning.

Mirzayans F, Mears AJ, Guo SW, Pearce WG, Walter MA. Mirzayans F, et al. Among authors: walter ma. Am J Hum Genet. 1997 Jul;61(1):111-9. doi: 10.1086/513894. Am J Hum Genet. 1997. PMID: 9245991 Free PMC article.

5

Autosomal dominant Axenfeld-Rieger anomaly maps to 6p25.

Gould DB, Mears AJ, Pearce WG, Walter MA. Gould DB, et al. Among authors: walter ma. Am J Hum Genet. 1997 Sep;61(3):765-8. Am J Hum Genet. 1997. PMID: 9326342 Free PMC article. No abstract available.

6

Mutation in the RIEG1 gene in patients with iridogoniodysgenesis syndrome.

Kulak SC, Kozlowski K, Semina EV, Pearce WG, Walter MA. Kulak SC, et al. Among authors: walter ma. Hum Mol Genet. 1998 Jul;7(7):1113-7. doi: 10.1093/hmg/7.7.1113. Hum Mol Genet. 1998. PMID: 9618168

7

Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly.

Mears AJ, Jordan T, Mirzayans F, Dubois S, Kume T, Parlee M, Ritch R, Koop B, Kuo WL, Collins C, Marshall J, Gould DB, Pearce W, Carlsson P, Enerbäck S, Morissette J, Bhattacharya S, Hogan B, Raymond V, Walter MA. Mears AJ, et al. Among authors: walter ma. Am J Hum Genet. 1998 Nov;63(5):1316-28. doi: 10.1086/302109. Am J Hum Genet. 1998. PMID: 9792859 Free PMC article.

8

Histopathology and molecular basis of iridogoniodysgenesis syndrome.

Pearce WG, Mielke BC, Kulak SC, Walter MA. Pearce WG, et al. Among authors: walter ma. Ophthalmic Genet. 1999 Jun;20(2):83-8. doi: 10.1076/opge.20.2.83.2294. Ophthalmic Genet. 1999. PMID: 10420192

9

Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25.

Mirzayans F, Gould DB, Héon E, Billingsley GD, Cheung JC, Mears AJ, Walter MA. Mirzayans F, et al. Among authors: walter ma. Eur J Hum Genet. 2000 Jan;8(1):71-4. doi: 10.1038/sj.ejhg.5200354. Eur J Hum Genet. 2000. PMID: 10713890

10

Isolation of a novel iris-specific and leucine-rich repeat protein (oculoglycan) using differential selection.

Friedman JS, Ducharme R, Raymond V, Walter MA. Friedman JS, et al. Among authors: walter ma. Invest Ophthalmol Vis Sci. 2000 Jul;41(8):2059-66. Invest Ophthalmol Vis Sci. 2000. PMID: 10892843

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