Detalhe da pesquisa
1.
National screening for Egyptian children aged 1 year up to 12 years at high risk of Autism and its determinants: a step for determining what ASD surveillance needs.
BMC Psychiatry
; 23(1): 471, 2023 06 28.
Artigo
Inglês
| MEDLINE | ID: mdl-37381024
2.
A national screening for the prevalence and profile of disability types among Egyptian children aged 6-12 years: a community-based population study.
BMC Public Health
; 23(1): 1599, 2023 08 22.
Artigo
Inglês
| MEDLINE | ID: mdl-37608272
3.
Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart Defects.
Pediatr Cardiol
; 39(5): 924-940, 2018 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-29541814
4.
Novel compound heterozygous mutations in MCPH1 gene causes primary microcephaly in Saudi family.
Neurosciences (Riyadh)
; 23(4): 347-350, 2018 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-30351297
5.
National screening for developmental delays and their determinants among Egyptian school age children: A step towards implementing life skills programs.
PLoS One
; 18(9): e0287315, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-37725608
6.
Sensitivity of DCSR3/GAPDH ratio using quantitative real-time PCR in the rapid prenatal diagnosis for down syndrome.
Fetal Diagn Ther
; 25(2): 220-3, 2009.
Artigo
Inglês
| MEDLINE | ID: mdl-19439973
7.
Molecular diagnosis of fragile X syndrome using methylation sensitive techniques in a cohort of patients with intellectual disability.
Pediatr Neurol
; 50(4): 368-76, 2014 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-24630283
8.
Mutational Analysis of the alpha-L-iduronidase gene in three Egyptian families: identification of three novel mutations and five novel polymorphisms.
Genet Test Mol Biomarkers
; 13(6): 761-4, 2009 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-19839758