| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Apolipoprotein E gene polymorphism in Egyptian acute coronary syndrome patients
|
Mahmoud, Aida A.
|
|
2016
|
17 |
1 |
p. 99-103
5 p.
|
artikel
|
| 2 |
Association of −308G/A TNF-α gene polymorphism and spontaneous preterm birth in Acehnese ethnic group, Indonesia: This polymorphism is not associated with preterm birth
|
Andalas, Mohd
|
|
2016
|
17 |
1 |
p. 33-40
8 p.
|
artikel
|
| 3 |
Baraitser–Winter syndrome: An additional Egyptian patient with skeletal anomalies, bilateral iris and choroid colobomas, retinal hypoplasia and hypoplastic scrotum
|
Shawky, Rabah M.
|
|
2016
|
17 |
1 |
p. 119-123
5 p.
|
artikel
|
| 4 |
Chromosomal abnormalities and autism
|
El-Baz, Farida
|
|
2016
|
17 |
1 |
p. 57-62
6 p.
|
artikel
|
| 5 |
Circulating cell free DNA as a predictor of systemic lupus erythematosus severity and monitoring of therapy
|
Hendy, Olfat M.
|
|
2016
|
17 |
1 |
p. 79-85
7 p.
|
artikel
|
| 6 |
Cyclooxygenase 1 (COX1) expression in Type 2 diabetes mellitus: A preliminary study from north India
|
Verma, Sushma
|
|
2016
|
17 |
1 |
p. 41-45
5 p.
|
artikel
|
| 7 |
Cytogenetic diagnosis of Roberts SC phocomelia syndrome: First report from Kashmir
|
Malla, Tahir M.
|
|
2016
|
17 |
1 |
p. 137-140
4 p.
|
artikel
|
| 8 |
Distribution of ABO blood groups and rhesus factor in a Large Scale Study of different cities and ethnicities in Khuzestan province, Iran
|
Torabizade maatoghi, J.
|
|
2016
|
17 |
1 |
p. 105-109
5 p.
|
artikel
|
| 9 |
Do the MTHFR gene polymorphism and Down syndrome pregnancy association stands true? A case–control study of Indian population and meta-analysis
|
Muthuswamy, Srinivasan
|
|
2016
|
17 |
1 |
p. 87-97
11 p.
|
artikel
|
| 10 |
Editorial Board
|
|
|
2016
|
17 |
1 |
p. iii-
1 p.
|
artikel
|
| 11 |
Exploring the link between VDR rs2228570 and uterine leiomyoma in Iranian women
|
Shahbazi, Shirin
|
|
2016
|
17 |
1 |
p. 115-118
4 p.
|
artikel
|
| 12 |
Frequency and pattern of cytogenetic alterations in primary amenorrhea cases of Kashmir, North India
|
Malla, Tahir M.
|
|
2016
|
17 |
1 |
p. 25-31
7 p.
|
artikel
|
| 13 |
Magnesium supplementation in children with attention deficit hyperactivity disorder
|
El Baza, Farida
|
|
2016
|
17 |
1 |
p. 63-70
8 p.
|
artikel
|
| 14 |
Opitz C syndrome: Trigonocephaly, mental retardation and craniofacial dysmorphism
|
Fierro, J.A. Avina
|
|
2016
|
17 |
1 |
p. 125-129
5 p.
|
artikel
|
| 15 |
Pathogenetics. An introductory review
|
Salem, Mohammad Saad Zaghloul
|
|
2016
|
17 |
1 |
p. 1-23
23 p.
|
artikel
|
| 16 |
Pilot study for early prognosis of Azoospermia in relation to Y-STR Profiling
|
Refaat, Ahmed M.
|
|
2016
|
17 |
1 |
p. 47-56
10 p.
|
artikel
|
| 17 |
Screening of a clinically and biochemically diagnosed SOD patient using exome sequencing: A case report with a mutations/variations analysis approach
|
Aghanoori, Mohamad-Reza
|
|
2016
|
17 |
1 |
p. 131-136
6 p.
|
artikel
|
| 18 |
α-4 subunit of nicotinic acetylcholine receptor polymorphisms exhibit no association with smoking behavior among Malay Males in Kelantan, Malaysia
|
Ruzilawati, A.B.
|
|
2016
|
17 |
1 |
p. 71-77
7 p.
|
artikel
|
| 19 |
Susceptibility to methamphetamine dependence associated with high transcriptional activity alleles of VNTR polymorphism in the promoter region of monoamine oxidase A (MAOA)
|
Saify, Khyber
|
|
2016
|
17 |
1 |
p. 111-114
4 p.
|
artikel
|
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