nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Alteration of rRNA gene copy number and expression in patients with intellectual disability and heteromorphic acrocentric chromosomes
|
Kolesnikova, Irina S. |
|
2018 |
19 |
2 |
p. 129-134 |
artikel |
2 |
Are we missing fucosidosis?
|
Elsayed, Solaf |
|
2018 |
19 |
2 |
p. 151-152 |
artikel |
3 |
Association of adiponectin gene (ADIPOQ) polymorphisms with measures of obesity in Nigerian young adults
|
Ogundele, Olusegun E. |
|
2018 |
19 |
2 |
p. 123-127 |
artikel |
4 |
Clinical Utility of promoter methylation of the tumor suppressor genes DKK3, and RASSF1A in breast cancer patients
|
Saied, Marwa H. |
|
2018 |
19 |
2 |
p. 87-90 |
artikel |
5 |
Correlation between cognitive function, gross motor skills and health – Related quality of life in children with Down syndrome
|
Abd El-Hady, Saly Said |
|
2018 |
19 |
2 |
p. 97-101 |
artikel |
6 |
Current strides in AAV-derived vectors and SIN channels further relieves the limitations of gene therapy
|
Odiba, A.S. |
|
2018 |
19 |
2 |
p. 69-75 |
artikel |
7 |
Detecting Mycoplasma pneumoniae infections in nasopharyngeal specimens from Paediatric patients with asthma exacerbations in Baghdad: A Polymerase Chain Reaction – Gene based study
|
Al-Janabi, Muhi Kadhem Wannas |
|
2018 |
19 |
2 |
p. 117-121 |
artikel |
8 |
Fetal MTHFR C677T polymorphism confers no susceptibility to Down syndrome: Evidence from meta-analysis
|
Rai, Vandana |
|
2018 |
19 |
2 |
p. 53-58 |
artikel |
9 |
First report of microcephaly-capillary malformations syndrome in Russia
|
Demikova, Nataliya S. |
|
2018 |
19 |
2 |
p. 147-150 |
artikel |
10 |
Hemochromatosis C282Y gene mutation as a potential susceptibility factor for iron-overload in Egyptian beta-thalassemia patients
|
Mokhtar, G.M. |
|
2018 |
19 |
2 |
p. 103-106 |
artikel |
11 |
Impact of migration on the expression of aggression and empathy in urban populations
|
Atramentova, Lubov |
|
2018 |
19 |
2 |
p. 83-86 |
artikel |
12 |
Multiplex polymerase chain reaction: Could change diagnosis of Ventilator-associated pneumonia in pediatric critical care units to the fast track?
|
Mansour, Mervat Gamal Eldin |
|
2018 |
19 |
2 |
p. 135-139 |
artikel |
13 |
R102G polymorphism of the complement component 3 gene in Malaysian subjects with neovascular age-related macular degeneration
|
Mohamad, Nur Afiqah |
|
2018 |
19 |
2 |
p. 77-81 |
artikel |
14 |
Robertsonian translocation 13/14 associated with rRNA genes overexpression and intellectual disability
|
Dolskiy, Alexander A. |
|
2018 |
19 |
2 |
p. 141-145 |
artikel |
15 |
Study of serum copper and ceruloplasmin levels in Egyptian autistic children
|
El-Baz, Farida |
|
2018 |
19 |
2 |
p. 113-116 |
artikel |
16 |
The endoplasmic reticulum stress response in disease pathogenesis and pathophysiology
|
Manalo, Rafael Vincent M. |
|
2018 |
19 |
2 |
p. 59-68 |
artikel |
17 |
The V279F polymorphism might change protein character and immunogenicity in Lp-PLA2 protein
|
Widodo, |
|
2018 |
19 |
2 |
p. 107-112 |
artikel |
18 |
XRCC1 Arg194Trp polymorphism is no risk factor for skin cancer development in Kashmiri population
|
Maqbool, Rouf |
|
2018 |
19 |
2 |
p. 91-95 |
artikel |