E-LIB Suche - Ergebnisse für: Yariz, Kemal O

1

Novel domain-specific POU3F4 mutations are associated with ..:

Bademci, Guney ; Lasisi, Akeem O ; Yariz, Kemal O...
BMC Medical Genetics. 16 (2015) 1 - p. , 2015

Link: https://doi.org/10.1186/..

2

An Amino Acid Deletion in SZT2 in a Family with Non-Syndrom..:

Falcone, Michelle ; Yariz, Kemal O. ; Ross, David B....
PLoS ONE. 8 (2013) 12 - p. e82810 , 2013

Link: https://doi.org/10.1371/..

3

Inherited mutation of the luteinizing hormone/choriogonadot..:

Yariz, Kemal O. ; Walsh, Tom ; Uzak, Asli...
Fertility and Sterility. 96 (2011) 2 - p. e125-e130 , 2011

Link: https://doi.org/10.1016/..

4

X-linked infantile spinal muscular atrophy: Clinical defini..:

Dressman, Devin ; Ahearn, Mary Ellen ; Yariz, Kemal O....
Genetics in Medicine. 9 (2007) 1 - p. 52-60 , 2007

Link: https://doi.org/10.1097/..

5

Novel Domain-Specific Pou3F4 Mutations Are Associated With ..:

Bademci, Guney ; Lasisi, Akeem O ; Yariz, Kemal O...
10.1186/s12881-015-0149-2. , 2015

Link: http://hdl.handle.net/11..

6

Mutations in OTOGL, Encoding the Inner Ear Protein Otogelin..:

Yariz, Kemal O ; Duman, Duygu ; Seco, Celia Zazo...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3487139. , 2012

Link: http://www.ncbi.nlm.nih...

7

Inherited mutation of the luteinizing hormone/choriogonadot..:

Yariz, Kemal O ; Walsh, Tom ; Uzak, Asli...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3143235. , 2011

Link: http://www.ncbi.nlm.nih...

8

A truncating mutation in GPSM2 is associated with recessive..:

Yariz, Kemal O ; Walsh, Tom ; Akay, Hatice...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3657750. , 2011

Link: http://www.ncbi.nlm.nih...

9

Rare Missense and Synonymous Variants in UBE1 Are Associate..:

Ramser, Juliane ; Ahearn, Mary Ellen ; Lenski, Claus...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2253959. , 2008

Link: http://www.ncbi.nlm.nih...

10

An amino acid deletion inSZT2 in a family with non-syndromi..:

Michelle Falcone ; Kemal O Yariz ; David B Ross...
http://europepmc.org/articles/PMC3855772?pdf=render. , 2013

Link: https://doi.org/10.1371/..

11

A homozygousSIX6mutation is associated with optic disc anom..:

Yariz, K.O. ; Sakalar, Y.B. ; Jin, X....
Clinical Genetics. 87 (2014) 2 - p. 192-195 , 2014

Link: https://doi.org/10.1111/..

12

Cardiomyopathy with alopecia and palmoplantar keratoderma (..:

Erken, H. ; Yariz, K.O. ; Duman, D....
British Journal of Dermatology. 165 (2011) 4 - p. 917-921 , 2011

Link: https://doi.org/10.1111/..

13

Effects of heterozygosity for the E180 splice mutation caus..:

Guevara-Aguirre, Jaime ; Rosenbloom, Arlan L. ; Guevara-Aguirre, Marco...
Growth Hormone & IGF Research. 17 (2007) 3 - p. 261-264 , 2007

Link: https://doi.org/10.1016/..