E-LIB Suche - Ergebnisse für: Alsahan, Nada

1

Missense Variants in GFRA1 and NPNT Are Associated with Con..:

Al-Hamed, Mohamed H. ; Sayer, John A. ; Alsahan, Nada...
Genes. 13 (2022) 10 - p. 1687 , 2022

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

2

A null founder variant in NPNT, encoding nephronectin, caus..:

Al‐Hamed, Mohamed H. ; Altuwaijri, Norah ; Alsahan, Nada...
Clinical Genetics. 102 (2022) 1 - p. 61-65 , 2022

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

3

Maternal Vitamin D Levels and Its Correlation With Low Birt..:

Almidani, Eyad ; Barkoumi, Abdullatif ; Elsaidawi, Weam...
Cureus. , 2021

Link: https://doi.org/10.7759/..

4

Prenatal exome sequencing and chromosomal microarray analys..:

Al-Hamed, Mohamed H. ; Kurdi, Wesam ; Khan, Rubina...
Human Genetics. 141 (2021) 1 - p. 101-126 , 2021

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

5

Lethal variants in humans: lessons learned from a large mol..:

Shamseldin, Hanan E. ; AlAbdi, Lama ; Maddirevula, Sateesh...
Genome Medicine. 13 (2021) 1 - p. , 2021

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

6

Novel loss of function variants in FRAS1 AND FREM2 underlie..:

Al-Hamed, Mohamed H. ; Sayer, John A. ; Alsahan, Nada...
Journal of Nephrology. 34 (2020) 3 - p. 893-900 , 2020

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

7

Fetal Anomalies Associated with Novel Pathogenic Variants i..:

Al-Hamed, Mohamed H. ; Alsahan, Nada ; Tulbah, Maha...
Genes. 11 (2020) 9 - p. 967 , 2020

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

8

ConfirmingTBC1D32‐related ciliopathy in humans:

Alsahan, Nada ; Alkuraya, Fowzan S.
American Journal of Medical Genetics Part A. 182 (2020) 8 - p. 1985-1987 , 2020

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

9

Bialleleic PKD1 mutations underlie early-onset autosomal do..:

Al-Hamed, Mohamed H. ; Alsahan, Nada ; Rice, Sarah J....
Pediatric Nephrology. 34 (2019) 9 - p. 1615-1623 , 2019

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

10

Molecular autopsy in maternal–fetal medicine:

Shamseldin, Hanan E. ; Kurdi, Wesam ; Almusafri, Fatima...
Genetics in Medicine. 20 (2018) 4 - p. 420-427 , 2018

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

11

Renal tubular dysgenesis: antenatal ultrasound scanning and..:

Al-Hamed, Mohamed H. ; Kurdi, Wesam ; Alsahan, Nada...
Clinical Kidney Journal. 9 (2016) 6 - p. 807-810 , 2016

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

12

Identification of embryonic lethal genes in humans by autoz..:

Shamseldin, Hanan E. ; Tulbah, Maha ; Kurdi, Wesam...
Genome Biology. 16 (2015) 1 - p. , 2015

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

13

Identification of a novel MKS locus defined byTMEM107mutati..:

Shaheen, Ranad ; Almoisheer, Agaadir ; Faqeih, Eissa...
Human Molecular Genetics. 24 (2015) 18 - p. 5211-5218 , 2015

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

14

Maternal floor infarction: Management of an underrecognized..:

Al‐Sahan, Nada ; Grynspan, David ; von Dadelszen, Peter.
Journal of Obstetrics and Gynaecology Research. 40 (2013) 1 - p. 293-296 , 2013

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

15

Missense Variants in GFRA1 and NPNT Are Associated with Con..:

Al-Hamed, Mohamed H ; Sayer, John A ; Alsahan, Nada...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9601797/. , 2022

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