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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1994 | 1 |
1995 | 1 |
1996 | 1 |
1997 | 1 |
1998 | 1 |
2001 | 1 |
2004 | 1 |
2024 | 0 |
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Page 1
Founder mutations of CYP1B1 gene in patients with congenital glaucoma from the United States and Brazil.
J Med Genet. 2004 Jan;41(1):e6. doi: 10.1136/jmg.2003.010777.
J Med Genet. 2004.
PMID: 14729846
Free PMC article.
No abstract available.
A gene responsible for the pigment dispersion syndrome maps to chromosome 7q35-q36.
Andersen JS, Pralea AM, DelBono EA, Haines JL, Gorin MB, Schuman JS, Mattox CG, Wiggs JL.
Andersen JS, et al.
Arch Ophthalmol. 1997 Mar;115(3):384-8. doi: 10.1001/archopht.1997.01100150386012.
Arch Ophthalmol. 1997.
PMID: 9076212
Item in Clipboard
A second locus for Rieger syndrome maps to chromosome 13q14.
Phillips JC, del Bono EA, Haines JL, Pralea AM, Cohen JS, Greff LJ, Wiggs JL.
Phillips JC, et al.
Am J Hum Genet. 1996 Sep;59(3):613-9.
Am J Hum Genet. 1996.
PMID: 8751862
Free PMC article.
Item in Clipboard
Clinical features of five pedigrees genetically linked to the juvenile glaucoma locus on chromosome 1q21-q31.
Wiggs JL, Del Bono EA, Schuman JS, Hutchinson BT, Walton DS.
Wiggs JL, et al.
Ophthalmology. 1995 Dec;102(12):1782-9. doi: 10.1016/s0161-6420(95)30793-2.
Ophthalmology. 1995.
PMID: 9098278
Item in Clipboard
Prevalence of mutations in TIGR/Myocilin in patients with adult and juvenile primary open-angle glaucoma.
Wiggs JL, Allingham RR, Vollrath D, Jones KH, De La Paz M, Kern J, Patterson K, Babb VL, Del Bono EA, Broomer BW, Pericak-Vance MA, Haines JL.
Wiggs JL, et al.
Am J Hum Genet. 1998 Nov;63(5):1549-52. doi: 10.1086/302098.
Am J Hum Genet. 1998.
PMID: 9792882
Free PMC article.
No abstract available.
Item in Clipboard
Molecular and clinical characterization of a patient with a chromosome 4p deletion, Wolf-Hirschhorn syndrome, and congenital glaucoma.
Finzi S, Pinto CF, Wiggs JL.
Finzi S, et al.
Ophthalmic Genet. 2001 Mar;22(1):35-41. doi: 10.1076/opge.22.1.35.2234.
Ophthalmic Genet. 2001.
PMID: 11262648
Item in Clipboard
Genetic linkage of autosomal dominant juvenile glaucoma to 1q21-q31 in three affected pedigrees.
Wiggs JL, Haines JL, Paglinauan C, Fine A, Sporn C, Lou D.
Wiggs JL, et al.
Genomics. 1994 May 15;21(2):299-303. doi: 10.1006/geno.1994.1269.
Genomics. 1994.
PMID: 8088822
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