Akarsu AN - Search Results

1

Phenotypic variability of triphalangeal thumb-polysyndactyly syndrome linked to chromosome 7q36.

Balci S, Demirtas M, Civelek B, Piskin M, Sensoz O, Akarsu AN. Balci S, et al. Among authors: akarsu an. Am J Med Genet. 1999 Dec 22;87(5):399-406. Am J Med Genet. 1999. PMID: 10594878

2

Hereditary intraosseous vascular malformation of the craniofacial region: an apparently novel disorder.

Vargel I, Cil BE, Er N, Ruacan S, Akarsu AN, Erk Y. Vargel I, et al. Among authors: akarsu an. Am J Med Genet. 2002 Apr 15;109(1):22-35. doi: 10.1002/ajmg.10282. Am J Med Genet. 2002. PMID: 11932989

3

Is vitamin D hypothesis for schizophrenia valid? Independent segregation of psychosis in a family with vitamin-D-dependent rickets type IIA.

Ozer S, Uluşahin A, Ulusoy S, Okur H, Coşkun T, Tuncali T, Göğüş A, Akarsu AN. Ozer S, et al. Among authors: akarsu an. Prog Neuropsychopharmacol Biol Psychiatry. 2004 Mar;28(2):255-66. doi: 10.1016/j.pnpbp.2003.10.002. Prog Neuropsychopharmacol Biol Psychiatry. 2004. PMID: 14751420

4

A clinically variant fibrosis syndrome in a Turkish family maps to the CFEOM1 locus on chromosome 12.

Sener EC, Lee BA, Turgut B, Akarsu AN, Engle EC. Sener EC, et al. Among authors: akarsu an. Arch Ophthalmol. 2000 Aug;118(8):1090-7. doi: 10.1001/archopht.118.8.1090. Arch Ophthalmol. 2000. PMID: 10922204

5

Clinical observations in autosomal recessive spastic paraplegia in childhood and further evidence for genetic heterogeneity.

Topaloğlu H, Pinarli G, Erdem H, Gücüyener K, Karaduman A, Topçu M, Akarsu AN, Ozgüç M. Topaloğlu H, et al. Among authors: akarsu an. Neuropediatrics. 1998 Aug;29(4):189-94. doi: 10.1055/s-2007-973559. Neuropediatrics. 1998. PMID: 9762694

6

Exclusion of primary congenital glaucoma (buphthalmos) from two candidate regions of chromosome arm 6p and chromosome 11.

Akarsu AN, Turacli ME, Aktan SG, Hossain A, Barsoum-Homsy M, Chevrette L, Sayli BS, Sarfarazi M. Akarsu AN, et al. Am J Med Genet. 1996 Jan 22;61(3):290-2. doi: 10.1002/(SICI)1096-8628(19960122)61:3<290::AID-AJMG16>3.0.CO;2-O. Am J Med Genet. 1996. PMID: 8741877 No abstract available.

7

A large Turkish kindred with syndactyly type II (synpolydactyly). 1. Field investigation, clinical and pedigree data.

Sayli BS, Akarsu AN, Sayli U, Akhan O, Ceylaner S, Sarfarazi M. Sayli BS, et al. Among authors: akarsu an. J Med Genet. 1995 Jun;32(6):421-34. doi: 10.1136/jmg.32.6.421. J Med Genet. 1995. PMID: 7666393 Free PMC article.

8

Mesoaxial complete syndactyly and synostosis with hypoplastic thumbs: an unusual combination or homozygous expression of syndactyly type I?

Percin EF, Percin S, Egilmez H, Sezgin I, Ozbas F, Akarsu AN. Percin EF, et al. Among authors: akarsu an. J Med Genet. 1998 Oct;35(10):868-74. doi: 10.1136/jmg.35.10.868. J Med Genet. 1998. PMID: 9783716 Free PMC article.

9

A large Turkish kindred with syndactyly type II (synpolydactyly). 2. Homozygous phenotype?

Akarsu AN, Akhan O, Sayli BS, Sayli U, Baskaya G, Sarfarazi M. Akarsu AN, et al. J Med Genet. 1995 Jun;32(6):435-41. doi: 10.1136/jmg.32.6.435. J Med Genet. 1995. PMID: 7666394 Free PMC article.

10

Nasopalpebral lipoma-coloboma syndrome.

Akarsu AN, Sayli BS. Akarsu AN, et al. Clin Genet. 1991 Nov;40(5):342-4. doi: 10.1111/j.1399-0004.1991.tb03106.x. Clin Genet. 1991. PMID: 1756608

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