E-LIB Suche - Ergebnisse für: Yousaf, Sairah

1

Transcriptional mapping of the macaque retina and RPE-choro..:

Mungale, Ameera ; McGaughey, David M. ; Zhang, Congxiao...
Frontiers in Genetics. 13 (2022) - p. , 2022

Link: https://doi.org/10.3389/..

2

Delineating the Molecular and Phenotypic Spectrum of the CN..:

Yousaf, Sairah ; Tariq, Nabeela ; Sajid, Zureesha...
Genes. 13 (2022) 4 - p. 617 , 2022

Link: https://doi.org/10.3390/..

3

Delineating the Molecular and Phenotypic Spectrum of the -R..:

Yousaf, Sairah ; Tariq, Nabeela ; Sajid, Zureesha...
Genes. , 2022

Link: http://hdl.handle.net/10..

4

Delineating the Molecular and Phenotypic Spectrum of the CN..:

Sairah Yousaf ; Nabeela Tariq ; Zureesha Sajid...
Molecular Genetics and Genomics. , 2022

Link: https://doi.org/10.3390/..

5

DataSheet1_Transcriptional mapping of the macaque retina an..:

Ameera Mungale ; David M. McGaughey ; Congxiao Zhang...
doi:10.3389/fgene.2022.949449.s001. , 2022

Link: https://doi.org/10.3389/..

6

Delineating the Molecular and Phenotypic Spectrum of the CN..:

Sairah Yousaf ; Nabeela Tariq ; Zureesha Sajid...
https://www.mdpi.com/2073-4425/13/4/617. , 2022

Link: https://doi.org/10.3390/..

7

Corneal structural changes in congenital glaucoma:

Drechsler, Jennifer ; Lee, Adrianna ; Maripudi, Snehaa...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8688203/. , 2022

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

8

Transcriptional mapping of the macaque retina and RPE-choro..:

Ameera Mungale ; David M. McGaughey ; Congxiao Zhang...
https://www.frontiersin.org/articles/10.3389/fgene.2022.949449/full. , 2022

Link: https://doi.org/10.3389/..

9

UBA2 variants underlie a recognizable syndrome with variabl..:

Schnur, Rhonda E. ; Yousaf, Sairah ; Liu, James...
Genetics in Medicine. 23 (2021) 9 - p. 1624-1635 , 2021

Link: https://doi.org/10.1038/..

10

Genetic Causes of Oculocutaneous Albinism in Pakistani Popu..:

Sajid, Zureesha ; Yousaf, Sairah ; Waryah, Yar M....
Genes. 12 (2021) 4 - p. 492 , 2021

Link: https://doi.org/10.3390/..

11

Novel Homozygous Missense Variant in GJA3 Connexin Domain C..:

Hassan, Abdullah Y. ; Yousaf, Sairah ; Levin, Moran R....
International Journal of Molecular Sciences. 23 (2021) 1 - p. 240 , 2021

Link: https://doi.org/10.3390/..

12

Novel Homozygous Missense Variant in GJA3 Connexin Domain C..:

Hassan, Abdullah Y ; Yousaf, Sairah ; Levin, Moran R...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745576/. , 2021

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

13

Novel Homozygous Missense Variant in Connexin Domain Causin..:

Hassan, Abdullah Y ; Yousaf, Sairah ; Levin, Moran R...
International Journal of Molecular Sciences. , 2021

Link: http://hdl.handle.net/10..

14

Genetic Causes of Oculocutaneous Albinism in Pakistani Popu..:

Zureesha Sajid ; Sairah Yousaf ; Yar M. Waryah...
Human Genomics and Genetic Diseases. , 2021

Link: https://doi.org/10.3390/..

15

UBA2 variants underlie a recognizable syndrome with variabl..:

Schnur, Rhonda E ; Yousaf, Sairah ; Liu, James...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8463496/. , 2021

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