A novel nonsense mutation in cathepsin C gene in an Egyptian patient presenting with Papillon–Lefèvre syndrome.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
Works matching IS 11108630 AND DT 2015 AND VI 16 AND IP 4
Results: 15
1
2
Clinical application of sensory integration therapy for children with autism.
- Published in:
- 2015
- By:
- Publication type:
- Letter to the Editor
3
Blepharophimosis, ptosis, epicanthus inversus syndrome type 2 with red hair, lymphedema of lower limbs and kidney stones in an Egyptian patient.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
4
Effectiveness of sensory integration program in motor skills in children with autism.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2015, v. 16, n. 4, p. 375, doi. 10.1016/j.ejmhg.2014.12.008
- By:
- Publication type:
- Article
5
Metabolic abnormalities in young Egyptian women with polycystic ovary syndrome and their relation to ADIPOQ gene variants and body fat phenotype.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2015, v. 16, n. 4, p. 367, doi. 10.1016/j.ejmhg.2015.05.007
- By:
- Publication type:
- Article
6
Association of glutathione-S-transferase P1 (GSTP1)-313 A > G gene polymorphism and susceptibility to endometrial hyperplasia among Egyptian women.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2015, v. 16, n. 4, p. 361, doi. 10.1016/j.ejmhg.2015.04.005
- By:
- Publication type:
- Article
7
Rhodopsin mutations are scarcely implicated in autosomal recessive retinitis pigmentosa: A preliminary study of Egyptian retinitis pigmentosa patients.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2015, v. 16, n. 4, p. 355, doi. 10.1016/j.ejmhg.2015.03.003
- By:
- Publication type:
- Article
8
Cancer ameliorating potential of Phyllanthus amarus: In vivo and in vitro studies against Aflatoxin B1 toxicity.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2015, v. 16, n. 4, p. 343, doi. 10.1016/j.ejmhg.2015.05.005
- By:
- Publication type:
- Article
9
Lipoprotein lipase gene variants: Association with acute myocardial infarction and lipid profiles.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2015, v. 16, n. 4, p. 327, doi. 10.1016/j.ejmhg.2015.04.001
- By:
- Publication type:
- Article
10
An overview on hepatitis C virus genotypes and its control.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2015, v. 16, n. 4, p. 291, doi. 10.1016/j.ejmhg.2015.05.003
- By:
- Publication type:
- Article
11
Patatin-like phospholipase domain containing-3 gene (PNPLA3) I148M polymorphism and liver damage in chronic hepatitis C Egyptian patients.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2015, v. 16, n. 4, p. 333, doi. 10.1016/j.ejmhg.2015.06.001
- By:
- Publication type:
- Article
12
The role of microRNAs on angiogenesis and vascular pressure in preeclampsia: The evidence from systematic review.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2015, v. 16, n. 4, p. 313, doi. 10.1016/j.ejmhg.2015.03.006
- By:
- Publication type:
- Article
13
Differential response of biochemical parameters to EMS and MMS treatments and their dose effect relationship on chromosomes in induced diabetic mouse.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2015, v. 16, n. 4, p. 301, doi. 10.1016/j.ejmhg.2015.05.004
- By:
- Publication type:
- Article
14
Radioactive fallout and neural tube defects.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2015, v. 16, n. 4, p. 299, doi. 10.1016/j.ejmhg.2015.06.007
- By:
- Publication type:
- Article
15
The relation between antihistamine medication during early pregnancy & birth defects.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2015, v. 16, n. 4, p. 287, doi. 10.1016/j.ejmhg.2015.04.003
- By:
- Publication type:
- Article