Percin EF - Search Results

1

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

2

Two unusual types of syndactyly in the same family; Cenani-Lenz type and "new" type versus severe type I syndactyly?

Percin EF, Percin S. Percin EF, et al. Among authors: percin s. Genet Couns. 2003;14(3):313-9. Genet Couns. 2003. PMID: 14577675

3

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

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

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.

6

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

7

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

8

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.

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

A case with bilateral radio-ulnar synostosis.

Koç A, Kaymak AO, Karaer K, Ergün MA, Aksu T, Perçin EF. Koç A, et al. Among authors: percin ef. Genet Couns. 2008;19(2):193-8. Genet Couns. 2008. PMID: 18618994 Review.

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