13 results on '"Farra, Chantal"'
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2. Novel missense mutation c.1784A>G, p.Tyr595Cys in RPS6KA3 gene responsible for Coffin–Lowry syndrome in a family with variable features and diabetes 2
3. Alpha Thalassemia Allelic Frequency in Lebanon
4. Changing frequency of equivocal HER-2/neu scores and factors predictive of negative HER 2/neu fluorescent in situ hybridisation in invasive carcinomas of the breast
5. Clinical and molecular analysis in families with autosomal recessive osteogenesis imperfecta identifies mutations in five genes and suggests genotype–phenotype correlations
6. An investigational ovarian stimulation protocol increased significantly the psychological burden in women with premature ovarian failure
7. Implementation of an intensive risk-stratified treatment protocol for children and adolescents with acute lymphoblastic leukemia in Lebanon
8. Intestinal polypoid arteriovenous malformation: unusual presentation in a child and review of the literature
9. Acceptance of preimplantation genetic diagnosis for β-thalassemia in Lebanese women with previously affected children
10. Familial Infantile Pyknocytosis in Association With Pulmonary Hypertension
11. Validation of a reverse-hybridization StripAssay for the simultaneous analysis of common α-thalassemia point mutations and deletions
12. A patient with duplication (7)(p22.1pter) characterized by array-CGH
13. Human Chromosome 7: DNA Sequence and Biology
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