Works matching IS 11108630 AND DT 2008 AND VI 9 AND IP 2
Results: 11
C Syndrome in an Egyptian infant with dilated brain ventricles and heterotopia.
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- Egyptian Journal of Medical Human Genetics, 2008, v. 9, n. 2, p. 257
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Holoprosencephaly: A report of 2 cases with different presentations.
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- Egyptian Journal of Medical Human Genetics, 2008, v. 9, n. 2, p. 249
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Frequency of fragile-x in x-linked mental retardation.
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- Egyptian Journal of Medical Human Genetics, 2008, v. 9, n. 2, p. 237
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Developmental abnormalities of mid and hindbrain: a study of 23 Egyptian patients.
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- Egyptian Journal of Medical Human Genetics, 2008, v. 9, n. 2, p. 215
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Paraoxonase 1 activity and genotyping in systemic lupus erythematosus and their relationships with cardiovascular complications.
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- Egyptian Journal of Medical Human Genetics, 2008, v. 9, n. 2, p. 201
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Phenotypic variability in patients with isodicentric Y(p11.3). A clinical, cytogenetic and molecular study.
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- Egyptian Journal of Medical Human Genetics, 2008, v. 9, n. 2, p. 189
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Cytokines and growth factors in Duchene muscular dystrophy patients.
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- Egyptian Journal of Medical Human Genetics, 2008, v. 9, n. 2, p. 181
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Genetic evaluation of proportionate short stature in Alexandria, Egypt.
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- Egyptian Journal of Medical Human Genetics, 2008, v. 9, n. 2, p. 171
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Craniofacial proportions and anthropometric measurements among growth hormone deficient Egyptian children.
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- Egyptian Journal of Medical Human Genetics, 2008, v. 9, n. 2, p. 161
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Haemochromatosis gene mutation H63D is a risk factor for iron overload in Egyptian beta- thalassemic children.
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- Egyptian Journal of Medical Human Genetics, 2008, v. 9, n. 2, p. 149
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Cholestasis in neonates and infants.
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- Egyptian Journal of Medical Human Genetics, 2008, v. 9, n. 2, p. 135
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- Article