Karaguzel A - Search Results

1

Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.

Celep F, Uzumcu A, Sonmez FM, Uyguner O, Balci YI, Bahadir S, Karaguzel A. Celep F, et al. Among authors: karaguzel a. Genet Couns. 2009;20(1):1-8. Genet Couns. 2009. PMID: 19400537

2

Ring chromosome 18 in a child with febrile seizures.

Celep F, Sonmez FM, Kul S, Ucar F, Karaguzel A. Celep F, et al. Among authors: karaguzel a. Genet Couns. 2011;22(2):165-71. Genet Couns. 2011. PMID: 21848009

3

Chromosomal abnormalities in 457 Turkish patients with MCA/MR.

Celep F, Sönmez FM, Karagüzel A. Celep F, et al. Among authors: karaguzel a. Turk J Pediatr. 2006 Apr-Jun;48(2):130-4. Turk J Pediatr. 2006. PMID: 16848112

4

Detection of an unbalanced t(4;15) by FISH in a child with multiple congenital anomalies.

Celep F, Acar H, Aynaci O, Aynaci FM, Karagüzel A. Celep F, et al. Among authors: karaguzel a. Genet Couns. 2001;12(4):319-26. Genet Couns. 2001. PMID: 11837600

5

The frequency of chromosomal abnormalities in patients with reproductive failure.

Celep F, Karagüzel A, Ozeren M, Bozkaya H. Celep F, et al. Among authors: karaguzel a. Eur J Obstet Gynecol Reprod Biol. 2006 Jul;127(1):106-9. doi: 10.1016/j.ejogrb.2005.12.019. Epub 2006 Jan 27. Eur J Obstet Gynecol Reprod Biol. 2006. PMID: 16443317

6

A case of VATER association associated with 9qh+.

Aynaci FM, Celep F, Karagüzel A, Baki A, Yildiran A. Aynaci FM, et al. Among authors: karaguzel a. Genet Couns. 1996;7(4):321-2. Genet Couns. 1996. PMID: 8985737 No abstract available.

7

A case report of 46,XX,del(21)(q22) de novo deletion associated with Imerslund-Grasbeck syndrome.

Celep F, Karagüzel A, Aynaci FM, Erduran E. Celep F, et al. Among authors: karaguzel a. Clin Genet. 1996 Oct;50(4):248-50. doi: 10.1111/j.1399-0004.1996.tb02637.x. Clin Genet. 1996. PMID: 9001810

8

Frequency of cardiovascular and gastrointestinal malformations, leukemia and hypothyroidism in children with Down syndrome in Trabzon, Turkey.

Aynaci FM, Orhan F, Celep F, Karagüzel A. Aynaci FM, et al. Among authors: karaguzel a. Turk J Pediatr. 1998 Jan-Mar;40(1):103-9. Turk J Pediatr. 1998. PMID: 9673536

9

Detection of chromosomal aberrations in prostate cancer by fluorescence in situ hybridization (FISH).

Celep F, Karagüzel A, Ozgür GK, Yildiz K. Celep F, et al. Among authors: karaguzel a. Eur Urol. 2003 Dec;44(6):666-71. doi: 10.1016/s0302-2838(03)00414-7. Eur Urol. 2003. PMID: 14644118

10

Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss.

Kalay E, Li Y, Uzumcu A, Uyguner O, Collin RW, Caylan R, Ulubil-Emiroglu M, Kersten FF, Hafiz G, van Wijk E, Kayserili H, Rohmann E, Wagenstaller J, Hoefsloot LH, Strom TM, Nürnberg G, Baserer N, den Hollander AI, Cremers FP, Cremers CW, Becker C, Brunner HG, Nürnberg P, Karaguzel A, Basaran S, Kubisch C, Kremer H, Wollnik B. Kalay E, et al. Among authors: karaguzel a. Hum Mutat. 2006 Jul;27(7):633-9. doi: 10.1002/humu.20368. Hum Mutat. 2006. PMID: 16752389

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

28 results

Search Page

Filters