E-LIB Suche - Ergebnisse für: Mazen, Inas M

1

An infertile azoospermic male with 45,X karyotype and a uni..:

Mekkawy, Mona K. ; El Guindi, Ahmed M. ; Mazen, Inas M....
Journal of Assisted Reproduction and Genetics. 35 (2018) 8 - p. 1503-1508 , 2018

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

2

Genotype/phenotype correlation in a female patient with 21q..:

Mekkawy, Mona K. ; Mazen, Inas M. ; Kamel, Alaa K...
American Journal of Medical Genetics Part A. 170 (2016) 4 - p. 1050-1058 , 2016

Link: https://doi.org/10.1002/..

3

An infertile azoospermic male with 45,X karyotype and a uni..:

Mekkawy, Mona K ; El Guindi, Ahmed M ; Mazen, Inas M...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6086791/. , 2018

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

4

Congenital leptin and leptin receptor deficiencies in nine ..:

Mazen, Inas H. ; El-Gammal, Mona A. ; Elaidy, Aya A....
Molecular Genetics and Genomics. 298 (2023) 4 - p. 919-929 , 2023

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

5

Chromosome 9p terminal deletion in nine Egyptian patients a..:

Mohamed, Amal M. ; Kamel, Alaa K. ; Eid, Maha M....
Molecular Genetics & Genomic Medicine. 9 (2021) 11 - p. , 2021

Link: https://doi.org/10.1002/..

6

IGF1R, IGFALS, and IGFBP3 gene copy number variations in a ..:

Fadel, Islam M. ; Ragab, Moustafa H. ; Eid, Ola M....
Journal of Genetic Engineering and Biotechnology. 19 (2021) 1 - p. 109 , 2021

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

7

Detection of low-grade mosaicism and its correlation with h..:

Madian, Abdelrahman ; Eid, Maha M. ; Shahin, Adel A.B....
Reproductive Biology. 20 (2020) 2 - p. 259-263 , 2020

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

8

Screening of the SHOX/PAR1 region using MLPA and miRNA expr..:

Eid, Ola M. ; Eid, Maha M. ; Abdelrahman, Amany H....
Egyptian Journal of Medical Human Genetics. 21 (2020) 1 - p. , 2020

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

9

Biallelic novel missense HHAT variant causes syndromic micr..:

Abdel‐Salam, Ghada M. H. ; Mazen, Inas ; Eid, Maha...
American Journal of Medical Genetics Part A. 179 (2019) 6 - p. 1053-1057 , 2019

Link: https://doi.org/10.1002/..

10

Identification of a novel homozygous ALX4 mutation in two u..:

El‐Ruby, Mona ; El‐Din Fayez, Alaa ; El‐Dessouky, Sara H....
American Journal of Medical Genetics Part A. 176 (2018) 5 - p. 1190-1194 , 2018

Link: https://doi.org/10.1002/..

11

GAPO syndrome in seven new patients: Identification of five..:

Abdel‐Hamid, Mohamed S. ; Ismail, Samira ; Zaki, Maha S....
American Journal of Medical Genetics Part A. 179 (2018) 2 - p. 237-242 , 2018

Link: https://doi.org/10.1002/..

12

Severe Early-Onset Obesity Due to Bioinactive Leptin Caused..:

Wabitsch, Martin ; Funcke, Jan-Bernd ; von Schnurbein, Julia...
The Journal of Clinical Endocrinology & Metabolism. 100 (2015) 9 - p. 3227-3230 , 2015

Link: https://doi.org/10.1210/..

13

IGF1R, IGFALS, and IGFBP3 gene copy number variations in a ..:

Fadel, Islam M ; Ragab, Moustafa H ; Eid, Ola M...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8319271/. , 2021

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

14

Chromosome 9p terminal deletion in nine Egyptian patients a..:

Mohamed, Amal M ; Kamel, Alaa K ; Eid, Maha M...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8606205/. , 2021

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

15

Severe Early-Onset Obesity Due to Bioinactive Leptin Caused..:

Wabitsch, Martin ; Funcke, Jan-Bernd ; von Schnurbein, Julia...
https://www.repository.cam.ac.uk/handle/1810/251446. , 2015

Link: https://www.repository.c..