Yuksel A - Search Results

1

A case of acampomelic campomelic dysplasia.

Ozkilic A, Seven M, Yuksel A. Ozkilic A, et al. Among authors: yuksel a. Genet Couns. 2002;13(1):23-8. Genet Couns. 2002. PMID: 12017234

2

Two female siblings with a previously unreported MCA/MR syndrome: pre- and postnatal growth retardation, iris colobomata, spasticity, facial dysmorphism and dilated ventricles.

Yüksel A, Seven M, Deviren A, Söylemez MA, Hacihanefioğlu S, Ulutin T, Cenani A. Yüksel A, et al. Genet Couns. 1999;10(3):265-9. Genet Couns. 1999. PMID: 10546098

3

A variant of Cenani-Lenz type syndactyly.

Seven M, Yüksel A, Ozkiliç A, Elçioğlu N. Seven M, et al. Among authors: yuksel a. Genet Couns. 2000;11(1):41-7. Genet Couns. 2000. PMID: 10756427

4

A case of symbrachydactyly with oligodactyly.

Seven M, Yuksel A, Ozkilic A. Seven M, et al. Among authors: yuksel a. Genet Couns. 2001;12(1):77-83. Genet Couns. 2001. PMID: 11332981

5

Trisomy 9p syndrome in two brothers: with new clinical findings and review of the literature.

Hacihanefioğlu S, Güven GS, Deviren A, Silahtaroğlu AN, Yosunvkaya Fenerci E, Ozkiliç A, Yüksel A. Hacihanefioğlu S, et al. Among authors: yuksel a. Genet Couns. 2002;13(1):41-8. Genet Couns. 2002. PMID: 12017237 Review.

6

A new syndrome presenting with dysmorphic facies, oculocutaneous albinism, glaucoma, cryptorchidism and mental retardation.

Seven M, Yosunkaya E, Yilmaz SB, Karaca E, Guven G, Yuksel A. Seven M, et al. Among authors: yuksel a. Genet Couns. 2011;22(1):25-34. Genet Couns. 2011. PMID: 21614985

7

Warburg Micro syndrome in a Turkish boy.

Yüksel A, Yesil G, Aras C, Seven M. Yüksel A, et al. Clin Dysmorphol. 2007 Apr;16(2):89-93. doi: 10.1097/MCD.0b013e328054c404. Clin Dysmorphol. 2007. PMID: 17351351

8

Dysmorphic face in two siblings with infantile neuroaxonal dystrophy.

Seven M, Ozkiliç A, Yüksel A. Seven M, et al. Among authors: yuksel a. Genet Couns. 2002;13(4):465-73. Genet Couns. 2002. PMID: 12558119

9

Joubert syndrome co-existing with partial Xp trisomy: review of the literature.

Güven GS, Fenerci EY, Deviren A, Ozkiliç A, Yüksel A, Hacihanefioğlu S. Güven GS, et al. Among authors: yuksel a. Genet Couns. 2004;15(3):321-8. Genet Couns. 2004. PMID: 15517825 Review.

10

Sudden vision loss in a mucopolysaccharidosis I patient receiving enzyme replacement therapy.

Yosunkaya E, Karaca E, Yilmaz SB, Gezdirici A, Guven G, Seven M, Yuksel A. Yosunkaya E, et al. Among authors: yuksel a. Genet Couns. 2011;22(4):371-6. Genet Couns. 2011. PMID: 22303797

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

392 results

Search Page