Gurkan H - Search Results

1

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

2

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

3

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.

4

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.

5

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.

6

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

7

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.

8

FOXF2 is required for cochlear development in humans and mice.

Bademci G, Abad C, Incesulu A, Elian F, Reyahi A, Diaz-Horta O, Cengiz FB, Sineni CJ, Seyhan S, Atli EI, Basmak H, Demir S, Nik AM, Footz T, Guo S, Duman D, Fitoz S, Gurkan H, Blanton SH, Walter MA, Carlsson P, Walz K, Tekin M. Bademci G, et al. Among authors: gurkan h. Hum Mol Genet. 2019 Apr 15;28(8):1286-1297. doi: 10.1093/hmg/ddy431. Hum Mol Genet. 2019. PMID: 30561639 Free PMC article.

9

Unusual facio-upper arm band of a fetus mimicking amniotic band syndrome.

Inan C, Sayin NC, Gurkan H, Erzincan SG, Uzun I, Sutcu H, Atli E, Varol F. Inan C, et al. Among authors: gurkan h. J Obstet Gynaecol Res. 2019 Apr;45(4):927-930. doi: 10.1111/jog.13905. Epub 2019 Jan 18. J Obstet Gynaecol Res. 2019. PMID: 30656803

10

Schizencephaly accompanied by occipital encephalocele and deletion of chromosome 22q13.32: a case report.

Inan C, Sayin NC, Gurkan H, Atli E, Gursoy Erzincan S, Uzun I, Sutcu H, Dogan S, Ikbal Atli E, Varol F. Inan C, et al. Among authors: gurkan h. Fetal Pediatr Pathol. 2019 Dec;38(6):496-502. doi: 10.1080/15513815.2019.1604921. Epub 2019 May 26. Fetal Pediatr Pathol. 2019. PMID: 31130048

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