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                             16 results found
no title author magazine year volume issue page(s) type
1 Absent abdominal muscles, nephro-urologic abnormalities, and severe neurologic damage in an infant with 3 chromosomal duplications: A novel syndrome? Akl, Kamal F.
2015
16 2 p. 195-197
3 p.
article
2 Berardinelli–Seip syndrome type 2 – An Egyptian child Shawky, Rabah M.
2015
16 2 p. 189-193
5 p.
article
3 Bicycle ergometer versus treadmill on balance and gait parameters in children with hemophilia Mohamed, Rasha A.
2015
16 2 p. 181-187
7 p.
article
4 Comparative frequency and allelic distribution of ABO and Rh (D) blood groups of major tribal communities of southern Bangladesh with general population and their determinants Dewan, Gourab
2015
16 2 p. 141-147
7 p.
article
5 Co-occurrence of Xp21 microduplication encompassing the DMD locus in conjunction with 17p12/PMP22 microduplication in a female with Charcot–Marie–Tooth disease type 1A Sidhu, Alpa
2015
16 2 p. 199-204
6 p.
article
6 Editorial Board 2015
16 2 p. iii-iv
nvt p.
article
7 Estimation of allelic frequencies for ABO and Rh blood groups Saadat, Mostafa
2015
16 2 p. 205-206
2 p.
article
8 Formal genetic maps Salem, Mohammad Saad Zaghloul
2015
16 2 p. 101-116
16 p.
article
9 Integrated effect of treadmill training combined with dynamic ankle foot orthosis on balance in children with hemiplegic cerebral palsy Sherief, Abd El Aziz Ali
2015
16 2 p. 173-179
7 p.
article
10 Multidisciplinary approach for evaluation of neurocutaneous disorders in children in Sohag University Hospital, Upper Egypt Sadek, Abdelrahim A.
2015
16 2 p. 149-157
9 p.
article
11 Prenatal genetic testing, counseling and follow-up of 33 Egyptian pregnant females with history of mucopolysaccharidoses Gaber, Khaled R.
2015
16 2 p. 159-163
5 p.
article
12 Selective screening in neonates suspected to have inborn errors of metabolism Shawky, Rabah M.
2015
16 2 p. 165-171
7 p.
article
13 SIRT1 gene is associated with cardiovascular disease in the Iranian population Mohtavinejad, N.
2015
16 2 p. 117-122
6 p.
article
14 Study of the effect of HFE gene mutations on iron overload in Egyptian thalassemia patients Wilson, Manal Michel
2015
16 2 p. 129-133
5 p.
article
15 The population structure of Ukraine in relation to the phenylthiocarbamide sensitivity Filiptsova, O.V.
2015
16 2 p. 135-139
5 p.
article
16 XmnI polymorphism: Relation to β-thalassemia phenotype and genotype in Egyptian Children Said, Fadwa
2015
16 2 p. 123-127
5 p.
article
                             16 results found
 
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