Gurkan H - Search Results

1

The Importance of Multiple Gene Analysis for Diagnosis and Differential Diagnosis in Charcot Marie Tooth Disease.

Yalcintepe S, Gurkan H, Dogan IG, Demir S, Sag SO, Kabayegit ZM, Atli EI, Atli E, Eker D, Temel SG. Yalcintepe S, et al. Among authors: gurkan h. Turk Neurosurg. 2021;31(6):888-895. doi: 10.5137/1019-5149.JTN.33661-21.3. Turk Neurosurg. 2021. PMID: 34169998 Free article.

2

The investigation of killer cell immunoglobulin-like receptor genotyping in patients with systemic lupus erytematosus and systemic sclerosis.

Tozkır JD, Tozkır H, Gürkan H, Dönmez S, Eker D, Pamuk GE, Pamuk ÖN. Tozkır JD, et al. Among authors: gurkan h. Clin Rheumatol. 2016 Apr;35(4):919-25. doi: 10.1007/s10067-016-3222-0. Epub 2016 Mar 9. Clin Rheumatol. 2016. PMID: 26960450

3

Tetrasomy 18p in a Twin Pregnancy with Diverse Expression in Both Fetuses.

Inan C, Sayın NC, Atlı E, Ulusal S, Erzincan S, Uzun I, Gurkan H, Varol FG. Inan C, et al. Among authors: gurkan h. Fetal Pediatr Pathol. 2016;35(5):339-343. doi: 10.1080/15513815.2016.1188870. Epub 2016 Jun 16. Fetal Pediatr Pathol. 2016. PMID: 27309155

4

A 9-year-old-girl with Phelan McDermid Syndrome, who had been diagnosed with an autism spectrum disorder.

Görker I, Gürkan H, Demir Ulusal S, Atlı E, Ikbal Atlı E. Görker I, et al. Among authors: gurkan h. Balkan J Med Genet. 2017 Mar 8;19(2):85-90. doi: 10.1515/bjmg-2016-0041. eCollection 2016 Dec 1. Balkan J Med Genet. 2017. PMID: 28289594 Free PMC article.

5

Genetic Analyses of the NF1 Gene in Turkish Neurofibromatosis Type I Patients and Definition of three Novel Variants.

Ulusal SD, Gürkan H, Atlı E, Özal SA, Çiftdemir M, Tozkır H, Karal Y, Güçlü H, Eker D, Görker I. Ulusal SD, et al. Among authors: gurkan h. Balkan J Med Genet. 2017 Jun 30;20(1):13-20. doi: 10.1515/bjmg-2017-0008. eCollection 2017 Jun 30. Balkan J Med Genet. 2017. PMID: 28924536 Free PMC article.

6

Identification of a novel homozygous TBC1D24 mutation in a Turkish family with DOORS syndrome.

Atli E, Gurkan H, Ulusal S, Karal Y, Atli EI, Tozkir H. Atli E, et al. Among authors: gurkan h. Clin Dysmorphol. 2018 Jan;27(1):1-3. doi: 10.1097/MCD.0000000000000204. Clin Dysmorphol. 2018. PMID: 29176366 No abstract available.

7

Prenatal diagnosis of chromosomal polymorphisms: most commonly observed polymorphism on Chromosome 9 have associations with low PAPP-A values.

Inan C, Sayin NC, Dolgun ZN, Gurkan H, Erzincan SG, Uzun I, Sutcu H, Ates S, Atli E, Varol F. Inan C, et al. Among authors: gurkan h. J Matern Fetal Neonatal Med. 2019 May;32(10):1688-1695. doi: 10.1080/14767058.2017.1416079. Epub 2017 Dec 20. J Matern Fetal Neonatal Med. 2019. PMID: 29262756 Free article.

8

A large posterior encephalocele associated with severe ventriculomegaly, cerebellar atrophy and transposition of the great arteries.

Inan C, Cenk Sayin N, Gurkan H, Erzincan SG, Uzun I, Sutcu H, Atli EI, Varol F. Inan C, et al. Among authors: gurkan h. J Clin Ultrasound. 2018 Nov;46(9):588-590. doi: 10.1002/jcu.22625. Epub 2018 Aug 14. J Clin Ultrasound. 2018. PMID: 30105815

9

Investigation of Copy Number Variation by arrayCGH in Turkish Children and Adolescents Diagnosed with Autism Spectrum Disorders.

Görker I, Gürkan H, Ulusal S, Atli E, Ayaz G, Ceylan C, Tozkir H, Altay MA, Erol A, Yildiz N, Direk C, Akköprü H, Kilit N, Aykutlu HC, Bozatli L, Çelik Z, Berberoğlu KK. Görker I, et al. Among authors: gurkan h. Noro Psikiyatr Ars. 2018 Apr 26;55(3):215-219. doi: 10.5152/npa.2017.21611. eCollection 2018 Sep. Noro Psikiyatr Ars. 2018. PMID: 30224866 Free PMC article.

10

Deletion of macro domain containing 2(MACRO D2) associated with transient hydrops fetalis.

Uzun Çilingir I, Sayin NC, Gurkan H, Çiftdemir NA, Atlı E, İnan C, Erzincan S, Sutcu H, Vatansever U, Varol F. Uzun Çilingir I, et al. Among authors: gurkan h. Taiwan J Obstet Gynecol. 2018 Dec;57(6):897-898. doi: 10.1016/j.tjog.2018.10.023. Taiwan J Obstet Gynecol. 2018. PMID: 30545550 Free article. No abstract available.

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