Caglayan AO - Search Results

1

Whole-exome sequencing identified a patient with TMCO1 defect syndrome and expands the phenotic spectrum.

Caglayan AO, Per H, Akgumus G, Gumus H, Baranoski J, Canpolat M, Calik M, Yikilmaz A, Bilguvar K, Kumandas S, Gunel M. Caglayan AO, et al. Clin Genet. 2013 Oct;84(4):394-5. doi: 10.1111/cge.12088. Epub 2013 Feb 20. Clin Genet. 2013. PMID: 23320496 Free PMC article. No abstract available.

2

A new patient with Andermann syndrome: an underdiagnosed clinical genetics entity?

Degerliyurt A, Akgumus G, Caglar C, Bilguvar K, Caglayan AO. Degerliyurt A, et al. Among authors: caglayan ao. Genet Couns. 2013;24(3):283-9. Genet Couns. 2013. PMID: 24341143

3

A provisionally unique syndrome with features including "molar tooth" sign and "femoral hypoplasia".

Caglayan AO, Gumus H, Yikilmaz A, Gumus GO, Per H. Caglayan AO, et al. Genet Couns. 2009;20(4):359-65. Genet Couns. 2009. PMID: 20162871

4

Autism with del15p.11.1: case report with a new cytogenetic finding.

Caglayan AO, Gumus H. Caglayan AO, et al. Genet Couns. 2010;21(2):199-204. Genet Couns. 2010. PMID: 20681220

5

A boy with classical Rubinstein-Taybi syndrome but no detectable mutation in the CREBBP and EP300 genes.

Caglayan AO, Lechno S, Gumus H, Bartsch O, Fryns JP. Caglayan AO, et al. Genet Couns. 2011;22(4):341-6. Genet Couns. 2011. PMID: 22303793

6

A unique case of a patient with partial trisomy 22 and lipodystrophy: is it a new syndrome due to an IGF-IR mutation?

Caglayan AO, Klammt J, Kiess W, Hatipoglu N, Pfäffle R, Kurtoglu S, Saatci C, Dundar M. Caglayan AO, et al. Genet Couns. 2010;21(2):187-97. Genet Couns. 2010. PMID: 20681219

7

A case with a rare chromosomal abnormality: isochromosome 18p.

Dundar M, Caglayan AO, Saatci C, Cetin Z, Arslan K, Uzak AS. Dundar M, et al. Among authors: caglayan ao. Genet Couns. 2010;21(1):69-74. Genet Couns. 2010. PMID: 20420032

8

Scoliosis, blindness and arachnodactyly in a large Turkish family: is it a new syndrome?

Dundar M, Erkilic K, Argun M, Caglayan AO, Comeglio P, Koseoglu E, Matyas G, Child AH. Dundar M, et al. Among authors: caglayan ao. Genet Couns. 2008;19(3):319-30. Genet Couns. 2008. PMID: 18990988 Free article.

9

Holt-Oram syndrome in two generations with translocation t(9;15)(p12;q11.2).

Caglayan AO, Koklu E, Saatci C, Gunes T, Ozkul Y, Narin N, Baykan A, Dundar M, Buyukkayhan D. Caglayan AO, et al. Ann Saudi Med. 2008 May-Jun;28(3):209-12. doi: 10.5144/0256-4947.2008.209. Ann Saudi Med. 2008. PMID: 18500176 Free PMC article. No abstract available.

10

Expression of WT1 gene in multiple myeloma patients at diagnosis: is WT1 gene expression a useful marker in multiple myeloma?

Saatci C, Caglayan AO, Kocyigit I, Akalin H, Kaynar LG, Altuntas F, Eser B, Demir M, Cetin M, Ozkul Y. Saatci C, et al. Among authors: caglayan ao. Hematology. 2010 Feb;15(1):39-42. doi: 10.1179/102453310X12583347009496. Hematology. 2010. PMID: 20132661 Free article.

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

94 results

Search Page

Filters