nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A novel MEFV gene mutation (A511V) in a Chilean FMF patient
|
Akar, Nejat |
|
2011 |
12 |
1 |
p. 21-24 4 p. |
artikel |
2 |
A study of new potential risk factors for Down syndrome in Upper Egypt
|
Shalaby, Hatem M.A. |
|
2011 |
12 |
1 |
p. 15-19 5 p. |
artikel |
3 |
Chromosomal study in newborn infants with congenital anomalies in Assiut University hospital: Cross-sectional study
|
Mohammed, Yasir A. |
|
2011 |
12 |
1 |
p. 79-90 12 p. |
artikel |
4 |
Clinico-epidemiologic characteristics of spinal muscular atrophy among Egyptians
|
Shawky, Rabah M. |
|
2011 |
12 |
1 |
p. 25-30 6 p. |
artikel |
5 |
Colchicine resistant FMF is not always true resistance
|
Ghaffar, Tawhida Y. Abdel |
|
2011 |
12 |
1 |
p. 99-101 3 p. |
artikel |
6 |
Congenital malformations prevalent among Egyptian children and associated risk factors
|
Shawky, Rabah M. |
|
2011 |
12 |
1 |
p. 69-78 10 p. |
artikel |
7 |
Connexin 26 (GJB2) mutation in KID syndrome: An Egyptian patient
|
Elsayed, Solaf M. |
|
2011 |
12 |
1 |
p. 91-93 3 p. |
artikel |
8 |
Educational Corner of the Issue
|
Zaky, Eman A. |
|
2011 |
12 |
1 |
p. 103-106 4 p. |
artikel |
9 |
Hemoglobin alpha 2 gene +861 G>A polymorphism in Turkish population
|
Dungul, Dilay Ciglidag |
|
2011 |
12 |
1 |
p. 59-62 4 p. |
artikel |
10 |
Hereditary multiple exostoses, macrocephaly, congenital heart disease, developmental delay, and mental retardation in a female patient: A possible new syndrome? Or new association?
|
Hamouda, Hanan I |
|
2011 |
12 |
1 |
p. 95-98 4 p. |
artikel |
11 |
Non HLA genetic markers association with type-1 diabetes mellitus
|
El-Ella, Soheir S. Abou |
|
2011 |
12 |
1 |
p. 39-47 9 p. |
artikel |
12 |
Nutritional genomics and personalized diet
|
Gaboon, Nagwa E.A. |
|
2011 |
12 |
1 |
p. 1-7 7 p. |
artikel |
13 |
Outcome of enzyme replacement therapy in children with Gaucher disease: The Egyptian experience
|
Khalifa, Ahmed S. |
|
2011 |
12 |
1 |
p. 9-14 6 p. |
artikel |
14 |
Porphyrins profile by high performance liquid chromatography/electrospray ionization tandem mass spectrometry for the diagnosis of porphyria
|
Fateen, E. |
|
2011 |
12 |
1 |
p. 49-58 10 p. |
artikel |
15 |
Risk factors for autism: An Egyptian study
|
El-Baz, Farida |
|
2011 |
12 |
1 |
p. 31-38 8 p. |
artikel |
16 |
Screening for subtle chromosomal rearrangements in an Egyptian sample of children with unexplained mental retardation
|
Shawky, Rabah M. |
|
2011 |
12 |
1 |
p. 63-68 6 p. |
artikel |