Héon E - Search Results

1

Further genetic heterogeneity for autosomal dominant human sutural cataracts.

Klopp N, Héon E, Billingsley G, Illig T, Wjst M, Rudolph G, Graw J. Klopp N, et al. Among authors: heon e. Ophthalmic Res. 2003 Mar-Apr;35(2):71-7. doi: 10.1159/000069134. Ophthalmic Res. 2003. PMID: 12646746 Free article.

2

Gene localization for aculeiform cataract, on chromosome 2q33-35.

Héon E, Liu S, Billingsley G, Bernasconi O, Tsilfidis C, Schorderet DF, Munier FL. Héon E, et al. Am J Hum Genet. 1998 Sep;63(3):921-6. doi: 10.1086/302005. Am J Hum Genet. 1998. PMID: 9718335 Free PMC article. No abstract available.

3

The gamma-crystallins and human cataracts: a puzzle made clearer.

Héon E, Priston M, Schorderet DF, Billingsley GD, Girard PO, Lubsen N, Munier FL. Héon E, et al. Am J Hum Genet. 1999 Nov;65(5):1261-7. doi: 10.1086/302619. Am J Hum Genet. 1999. PMID: 10521291 Free PMC article.

4

Genetic heterogeneity of the Coppock-like cataract: a mutation in CRYBB2 on chromosome 22q11.2.

Gill D, Klose R, Munier FL, McFadden M, Priston M, Billingsley G, Ducrey N, Schorderet DF, Héon E. Gill D, et al. Among authors: heon e. Invest Ophthalmol Vis Sci. 2000 Jan;41(1):159-65. Invest Ophthalmol Vis Sci. 2000. PMID: 10634616

5

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: heon e. Eur J Hum Genet. 2000 Jan;8(1):71-4. doi: 10.1038/sj.ejhg.5200354. Eur J Hum Genet. 2000. PMID: 10713890

6

A progressive autosomal recessive cataract locus maps to chromosome 9q13-q22.

Héon E, Paterson AD, Fraser M, Billingsley G, Priston M, Balmer A, Schorderet DF, Verner A, Hudson TJ, Munier FL. Héon E, et al. Am J Hum Genet. 2001 Mar;68(3):772-7. doi: 10.1086/318798. Epub 2001 Feb 5. Am J Hum Genet. 2001. PMID: 11179024 Free PMC article.

7

Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomaly.

Vincent A, Billingsley G, Priston M, Williams-Lyn D, Sutherland J, Glaser T, Oliver E, Walter MA, Heathcote G, Levin A, Héon E. Vincent A, et al. Among authors: heon e. J Med Genet. 2001 May;38(5):324-6. doi: 10.1136/jmg.38.5.324. J Med Genet. 2001. PMID: 11403040 Free PMC article. No abstract available.

8

Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier gene.

Vincent AL, Billingsley G, Buys Y, Levin AV, Priston M, Trope G, Williams-Lyn D, Héon E. Vincent AL, et al. Among authors: heon e. Am J Hum Genet. 2002 Feb;70(2):448-60. doi: 10.1086/338709. Epub 2002 Jan 3. Am J Hum Genet. 2002. PMID: 11774072 Free PMC article.

9

A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract.

Willoughby CE, Arab S, Gandhi R, Zeinali S, Arab S, Luk D, Billingsley G, Munier FL, Héon E. Willoughby CE, et al. Among authors: heon e. J Med Genet. 2003 Nov;40(11):e124. doi: 10.1136/jmg.40.11.e124. J Med Genet. 2003. PMID: 14627691 Free PMC article. No abstract available.

10

Defining the pathogenicity of optineurin in juvenile open-angle glaucoma.

Willoughby CE, Chan LL, Herd S, Billingsley G, Noordeh N, Levin AV, Buys Y, Trope G, Sarfarazi M, Héon E. Willoughby CE, et al. Among authors: heon e. Invest Ophthalmol Vis Sci. 2004 Sep;45(9):3122-30. doi: 10.1167/iovs.04-0107. Invest Ophthalmol Vis Sci. 2004. PMID: 15326130

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