Percin S - Search Results

1

Autosomal recessive mesoaxial synostotic syndactyly with phalangeal reduction maps to chromosome 17p13.3.

Malik S, Percin FE, Ahmad W, Percin S, Akarsu NA, Koch MC, Grzeschik KH. Malik S, et al. Among authors: percin fe, percin s. Am J Med Genet A. 2005 May 1;134(4):404-8. doi: 10.1002/ajmg.a.30656. Am J Med Genet A. 2005. PMID: 15779011

2

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: percin s. 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.

3

Spondyloepiphyseal dysplasia tarda with progressive arthropathy.

Kaptanoğlu E, Perçin F, Perçin S, Törel-Ergür A. Kaptanoğlu E, et al. Among authors: percin f, percin s. Turk J Pediatr. 2004 Oct-Dec;46(4):380-3. Turk J Pediatr. 2004. PMID: 15641278

4

Larsen's syndrome with mixed-type hearing loss.

Perçín EF, Perçín S, Sezgin I, Akbas AK. Perçín EF, et al. Among authors: percin s. Acta Orthop Belg. 1994;60(3):328-31. Acta Orthop Belg. 1994. PMID: 7992613

5

Surgical risk factors in Larsen's syndrome.

Karakas K, Percin EF, Percin S. Karakas K, et al. Among authors: percin ef, percin s. Acta Orthop Belg. 2000 Dec;66(5):495-8. Acta Orthop Belg. 2000. PMID: 11196375

6

A case with Pyle type metaphyseal dysplasia: clinical, radiological and histological evaluation.

Percin EF, Percin S, Koptagel E, Demirel H. Percin EF, et al. Among authors: percin s. Genet Couns. 2003;14(4):387-93. Genet Couns. 2003. PMID: 14738111

7

A case with spondylo-metaphyseal dysplasia type A4.

Percin EF, Tukenmez M, Percin S. Percin EF, et al. Among authors: percin s. Genet Couns. 2004;15(3):363-9. Genet Couns. 2004. PMID: 15517830

8

First-trimester diagnosis of Robinow syndrome.

Percin EF, Guvenal T, Cetin A, Percin S, Goze F, Arici S. Percin EF, et al. Among authors: percin s. Fetal Diagn Ther. 2001 Sep-Oct;16(5):308-11. doi: 10.1159/000053933. Fetal Diagn Ther. 2001. PMID: 11509854

9

A new combination: short stature, congenital unilateral absence of the fibula, oligodactyly and trigonocephaly.

Perçin EF, Perçin S. Perçin EF, et al. Among authors: percin s. Clin Dysmorphol. 1999 Jan;8(1):67-8. Clin Dysmorphol. 1999. PMID: 10327255 No abstract available.

10

Waardenburg syndrome type I and small patella syndrome in the same patient.

Perçin EF, Bulut S, Kunt T, Perçin S, Bulut O, Süngü S. Perçin EF, et al. Among authors: percin s. Pediatr Int. 1999 Dec;41(6):704-6. doi: 10.1046/j.1442-200x.1999.01133.x. Pediatr Int. 1999. PMID: 10618897 No abstract available.

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