E-LIB Suche - Ergebnisse für: Elsobky, Ezzat S

1

Disorders of Sex Determination:

, In: Genetics of Male Infertility,

Abdel-Hamid, Ibrahim A. ; Elsobky, Ezzat S. ; Elsaied, Moustafa A. - p. 279-299 , 2020

Link: https://doi.org/10.1007/..

2

Phenotypic and Genetic Characterization of a Cohort of Pedi..:

Abdel Ghaffar, Tawhida Y ; Elsayed, Solaf M ; Elnaghy, Suzan...
BMC Pediatrics. 11 (2011) 1 - p. , 2011

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

3

Cholestasis in patients with Cockayne syndrome and suggeste..:

Abdel Ghaffar, Tawhida Y ; Elsobky, Ezzat S ; Elsayed, Solaf M
Orphanet Journal of Rare Diseases. 6 (2011) 1 - p. , 2011

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

4

Screening for subtle chromosomal rearrangements in an Egypt..:

Shawky, Rabah M. ; El-Baz, Farida ; Elsobky, Ezzat S....
Egyptian Journal of Medical Human Genetics. 12 (2011) 1 - p. 63-68 , 2011

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

5

Cytogenetic aberrations and the development of uterine leio..:

El‐Gharib, Mohamed N. ; Elsobky, Ezzat S.
Journal of Obstetrics and Gynaecology Research. 36 (2010) 1 - p. 101-107 , 2010

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

6

Phenotypic and Genetic Characterization of a Cohort of Pedi..:

Elnaghy Suzan ; Elsayed Solaf M ; Abdel Ghaffar Tawhida Y...
http://www.biomedcentral.com/1471-2431/11/56. , 2011

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

7

Cholestasis in patients with Cockayne syndrome and suggeste..:

Elsobky Ezzat S ; Abdel Ghaffar Tawhida Y ; Elsayed Solaf M
http://www.ojrd.com/content/6/1/13. , 2011

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

8

Phenotypic and Genetic Characterization of a Cohort of Pedi..:

Abdel Ghaffar, Tawhida Y ; Elsayed, Solaf M ; Elnaghy, Suzan...
http://www.biomedcentral.com/1471-2431/11/56. , 2011

Link: http://www.biomedcentral..

9

Cholestasis in patients with Cockayne syndrome and suggeste..:

Abdel Ghaffar, Tawhida Y ; Elsobky, Ezzat S ; Elsayed, Solaf M
http://www.ojrd.com/content/6/1/13. , 2011

Link: http://www.ojrd.com/cont..

10

Non-manifesting AHI1 truncations indicate localized loss-of..:

Elsayed, Solaf M. ; Phillips, Jennifer B. ; Heller, Raoul...
Human Molecular Genetics. 24 (2015) 9 - p. 2594-2603 , 2015

Link: https://doi.org/10.1093/..

11

Factor V G1691A (Leiden) is a major etiological factor in E..:

Tawhida Y. Abdel Ghaffar ; Solaf M. Elsayed ; Mohamed A. Sakr...
http://www.journalagent.com/z4/download_fulltext.asp?pdir=tjh&plng=eng&un=TJH-87360. , 2011

Link: https://doaj.org/article..

12

Factor V G1691A (Leiden) is a major etiological factor in E..:

Tawhida Y. Abdel Ghaffar ; Solaf M. Elsayed ; Mohamed A. Sakr...
https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tjh&un=TJH-87360. , 2011

Link: https://doi.org/10.5152/..

13

Autosomal dominant SCA5 and autosomal recessive infantile S..:

Elsayed, Solaf M ; Heller, Raoul ; Thoenes, Michaela...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC. , 2014

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

14

Vascular endothelial growth factor +405G/C polymorphism as ..:

Amer, Azza K. ; Khalaf, Nervana A. ; Aboelmakarem, Safia H....
Bulletin of the National Research Centre. 44 (2020) 1 - p. , 2020

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

15

Role of advanced glycation end products and sorbitol dehydr..:

Moemen, Leqaa A. ; Abdel Hamid, Mona A. ; Wahab, Soher Abdel...
Bulletin of the National Research Centre. 44 (2020) 1 - p. , 2020

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