Meyer BF - Search Results

1

Allelic heterogeneity in inbred populations: the Saudi experience with Alström syndrome as an illustrative example.

Aldahmesh MA, Abu-Safieh L, Khan AO, Al-Hassnan ZN, Shaheen R, Rajab M, Monies D, Meyer BF, Alkuraya FS. Aldahmesh MA, et al. Among authors: meyer bf. Am J Med Genet A. 2009 Feb 15;149A(4):662-5. doi: 10.1002/ajmg.a.32753. Am J Med Genet A. 2009. PMID: 19283855

2

Pellucid marginal degeneration coexistent with cornea plana in one member of a family exhibiting a novel KERA mutation.

Khan AO, Aldahmesh M, Al-Saif A, Meyer B. Khan AO, et al. Br J Ophthalmol. 2005 Nov;89(11):1538-40. doi: 10.1136/bjo.2005.073510. Br J Ophthalmol. 2005. PMID: 16234475 Free PMC article. No abstract available.

3

Novel PRG4 mutations underlie CACP in Saudi families.

Alazami AM, Al-Mayouf SM, Wyngaard CA, Meyer B. Alazami AM, et al. Hum Mutat. 2006 Feb;27(2):213. doi: 10.1002/humu.9399. Hum Mutat. 2006. PMID: 16429407

4

Novel mutations underlying nephrogenic diabetes insipidus in Arab families.

Carroll P, Al-Mojalli H, Al-Abbad A, Al-Hassoun I, Al-Hamed M, Al-Amr R, Butt AI, Meyer BF. Carroll P, et al. Among authors: meyer bf. Genet Med. 2006 Jul;8(7):443-7. doi: 10.1097/01.gim.0000223554.46981.7a. Genet Med. 2006. PMID: 16845277 Free article.

5

Recessive cornea plana in the Kingdom of Saudi Arabia.

Khan AO, Aldahmesh M, Meyer B. Khan AO, et al. Ophthalmology. 2006 Oct;113(10):1773-8. doi: 10.1016/j.ophtha.2006.04.026. Ophthalmology. 2006. PMID: 17011957

6

Familial blepharophimosis-like syndrome with esotropia, uveal coloboma, and short stature.

Khan AO, Alam SK, Aldahmesh M, Rajab M, Meyer B. Khan AO, et al. Ophthalmic Genet. 2006 Sep;27(3):79-82. doi: 10.1080/13816810600862501. Ophthalmic Genet. 2006. PMID: 17050282

7

Corneal ectasia and hydrops in a patient with autosomal recessive cornea plana.

Khan AO, Aldahmesh M, Meyer B. Khan AO, et al. Ophthalmic Genet. 2006 Sep;27(3):99-101. doi: 10.1080/13816810600862469. Ophthalmic Genet. 2006. PMID: 17050286

8

Mutations underlying 3-hydroxy-3-methylglutaryl CoA lyase deficiency in the Saudi population.

Al-Sayed M, Imtiaz F, Alsmadi OA, Rashed MS, Meyer BF. Al-Sayed M, et al. Among authors: meyer bf. BMC Med Genet. 2006 Dec 16;7:86. doi: 10.1186/1471-2350-7-86. BMC Med Genet. 2006. PMID: 17173698 Free PMC article.

9

The enhanced S-cone syndrome in children.

Khan AO, Aldahmesh M, Meyer B. Khan AO, et al. Br J Ophthalmol. 2007 Mar;91(3):394-6. doi: 10.1136/bjo.2006.097956. Br J Ophthalmol. 2007. PMID: 17322467 Free PMC article. No abstract available.

10

The T/G 13915 variant upstream of the lactase gene (LCT) is the founder allele of lactase persistence in an urban Saudi population.

Imtiaz F, Savilahti E, Sarnesto A, Trabzuni D, Al-Kahtani K, Kagevi I, Rashed MS, Meyer BF, Järvelä I. Imtiaz F, et al. Among authors: meyer bf. J Med Genet. 2007 Oct;44(10):e89. doi: 10.1136/jmg.2007.051631. J Med Genet. 2007. PMID: 17911653 Free PMC article.

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