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Results of search for 'au:"Otaify, G"'
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Authors
Abdel-Ghafar, S F
Abdel-Hamid, M S
Aboul-Ezz, E
Aboul-Ezz, E H A
Aglan, M S
El Banna, R A S
Elbendary, H M
Eldarsh, A
Elhadidi, S M A
Elnashar, M
Elruby, M
Essawi, M
Farouk, D
Fayez, A
Gaber, K
Hassan, H
Mehrez, M I
Otaify, G A
Temtamy, S A
Zaki, M S
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Topics
Abnormalities, Multiple
Acetyltransferases
Adolescent
Adult
Base Sequence
Bone Density
Child
Child, Preschool
Consanguinity
DNA Mutational Analysis
Egypt
Female
Founder Effect
Humans
Infant
Male
Pedigree
Phenotype
genetics
methods
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English
Your search returned 4 results.
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1.
Zoledronic acid in children with osteogenesis imperfecta and Bruck syndrome: a 2-year prospective observational study.
[electronic resource]
by
Otaify, G A
Aglan, M S
Ibrahim, M M
Elnashar, M
El Banna, R A S
Temtamy, S A
Producer:
20161024
In:
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA
vol. 27
Online resources:
Available from publisher's website
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No items available.
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2.
PGAP3-related hyperphosphatasia with mental retardation syndrome: Report of 10 new patients and a homozygous founder mutation.
[electronic resource]
by
Abdel-Hamid, M S
Issa, M Y
Otaify, G A
Abdel-Ghafar, S F
Elbendary, H M
Zaki, M S
Producer:
20180806
In:
Clinical genetics
vol. 93
Online resources:
Available from publisher's website
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No items available.
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3.
Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect.
[electronic resource]
by
Otaify, G A
Abdel-Hamid, M S
Mehrez, M I
Aboul-Ezz, E
Zaki, M S
Aglan, M S
Temtamy, S A
Producer:
20191118
In:
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA
vol. 29
Online resources:
Available from publisher's website
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No items available.
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4.
ROBERTS SYNDROME: CLINICAL AND CYTOGENETIC STUDIES IN 8 EGYPTIAN PATIENTS AND MOLECULAR STUDIES IN 4 PATIENTS WITH GENOTYPE/PHENOTYPE CORRELATION.
[electronic resource]
by
Ismail, S
Essawi, M
Sedky, N
Hassan, H
Fayez, A
Helmy, N
Shehab, M
Farouk, D
Elruby, M
Otaify, G
Eldarsh, A
Hosny, L
Gaber, K
Aboul-Ezz, E H A
Ramzy, M I
Mehrez, M I
Hassib, N F
Elhadidi, S M A
Aglan, M S
Temtamy, S A
Producer:
20181016
In:
Genetic counseling (Geneva, Switzerland)
vol. 27
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