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PubPharm (1.077)
1021
Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3)
enthalten in:
Human genetics
| 2008
von
Azeem, Z.
|
Jelani, M.
|
Naz, G.
| +10
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1022
Knowledge about osteoporosis among healthy women attending a tertiary care hospital
enthalten in:
JPMA. The Journal of the Pakistan Medical Association
| 2008
von
Riaz, M.
|
Abid, N.
|
Patel, J.
| +3
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1023
N-Methyl-1-oxoisoindoline-2-carboxamide monohydrate
enthalten in:
Acta crystallographica. Section E, Structure reports online
| 2008
von
Maliha, B.
|
Tariq, M.
|
Tahir, M.
| +2
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1024
Preventive medicine practices by primary care providers in Karachi
enthalten in:
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP
| 2008
von
Patel, M.
|
Salahuddin, N.
|
Kashif, W.
| +7
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1025
1-Oxoisoindoline-2-carboxamide
enthalten in:
Acta crystallographica. Section E, Structure reports online
| 2008
von
Maliha, B.
|
Hussain, I.
|
Tahir, M.
| +2
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1026
A syndromic form of autosomal recessive congenital microcephaly (Jawad syndrome) maps to chromosome 18p11.22-q11.2
enthalten in:
Human genetics
| 2008
von
Hassan, M.
|
Chishti, M.
|
Jamal, S.
| +2
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1027
Synthesis, characterization and hypoglycemic activity of Zn(II), Cd(II) and Hg(II) complexes with glibenclamide
enthalten in:
Chemical & pharmaceutical bulletin
| 2008
von
Rasheed, K.
|
Tariq, M.
|
Munir, C.
| +2
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1028
Mutations of ESRRB encoding estrogen-related receptor beta cause autosomal-recessive nonsyndromic hearing impairment DFNB35
enthalten in:
American journal of human genetics
| 2008
von
Collin, R.
|
Kalay, E.
|
Tariq, M.
| +26
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1029
Beta-hemolytic streptococcus group A endocarditis : a rare clinical presentation
enthalten in:
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP
| 2008
von
Almas, A.
|
Tariq, M.
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1030
A novel missense mutation in the EDA gene associated with X-linked recessive isolated hypodontia
enthalten in:
Journal of human genetics
| 2008
von
Rasool, M.
|
Schuster, J.
|
Aslam, M.
| +6
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