Articles in Scholarly Journals [Incomplete List]

1. A patient with duplication (7)(p22.1pter) characterized by array-CGH
   American Journal of Medical Genetics Part A, vol. 143A, no. 2, pp. 168–171, 2007
2. Outcome of chromosomally abnormal pregnancies in Lebanon: obstetricians' roles during and after prenatal diagnosis
   Prenatal Diagnosis, vol. 27, no. 6, pp. 525–534, 2007
3. Caution in the Interpretation of ‘Mosaic’ Prenatal Karyotypes
   Fetal Diagnosis and Therapy, vol. 22, no. 1, pp. 80–80, 2007
4. Disruption of POF1B Binding to Nonmuscle Actin Filaments Is Associated with Premature Ovarian Failure
   The American Journal of Human Genetics, vol. 79, no. 1, pp. 113–119, 2006
5. To the Editor
   Annals of Human Genetics, vol. 70, no. 5, pp. 693–694, 2006
6. Prevalence of factor V Leiden, prothrombin and methylene tetrahydrofolate reductase mutations in women with adverse pregnancy outcomes in Lebanon
   American Journal of Obstetrics and Gynecology, vol. 195, no. 4, pp. 1114–1118, 2006
7. Linkage and mutational analysis of the CDAN1 gene reveals genetic heterogeneity in congenital dyserythropoietic anemia type I
   Blood, vol. 107, no. 12, pp. 4968–4969, 2006
8. Regression of Skeletal Manifestations of Hyperparathyroidism with Oral Vitamin D
   Journal of Clinical Endocrinology & Metabolism, vol. 91, no. 7, pp. 2480–2483, 2006
9. Apolipoprotein E Gene Polymorphism and Allele Frequencies in the Lebanese Population
   Molecular Biology Reports, vol. 33, no. 2, pp. 145–149, 2006
10. Molecular basis of oculocutaneous albinism type 1 in Lebanese patients
    Journal of Human Genetics, vol. 50, no. 6, pp. 317–319, 2005
11. Leydig cell hypoplasia due to inactivation of luteinizing hormone receptor by a novel homozygous nonsense truncation mutation in the seventh transmembrane domain
    Molecular and Cellular Endocrinology, vol. 229, no. 1-2, pp. 57–64, 2005
12. Potential trisomy 21 misdiagnosis by amniocentesis due to a resorbed twin
    Prenatal Diagnosis, vol. 24, no. 12, pp. 1013–1013, 2004
13. A new patient with pure trisomy 4p resulting from isochromosome formation and whole arm translocation
    American Journal of Medical Genetics, vol. 128A, no. 1, pp. 60–62, 2004
14. Ring chromosome 18q and jumping translocation 18p in an adult male with hypergonadotrophic hypogonadism
    American Journal of Medical Genetics, vol. 129A, no. 1, pp. 25–28, 2004
15. Attitudes towards prenatal diagnosis and termination of pregnancy among health professionals in Lebanon
    Prenatal Diagnosis, vol. 22, no. 10, pp. 880–886, 2002
16. Homologous telomere association of 19q in a female with premature ovarian failure
    Clinical Genetics, vol. 62, no. 4, pp. 310–314, 2002
17. Origin and History of the IVS-I-110 and Codon 39 [beta]-Thalassemia Mutations in the Lebanese Population
    Human Biology, vol. 74, no. 6, pp. 837–847, 2002
18. The Spectrum of ß-Thalassemia Mutations in the Arab Populations
    Journal of Biomedicine and Biotechnology, vol. 1, no. 3, pp. 129–132, 2001
19. Effect of oral iron chelation therapy with deferiprone (L1) on the psychosocial status of thalassaemia patients
    Haematologia, vol. 31, no. 4, pp. 333–339, 2001
20. Chromosome 10p11.2-p12.2 duplication: Report of a patient and review of the literature
    American Journal of Medical Genetics, vol. 104, no. 3, pp. 204–208, 2001
21. beta-Thalassaemia intermedia in Lebanon
    European Journal of Haematology, vol. 64, no. 4, pp. 237–244, 2000
22. A familial case of recurrent hydatidiform molar pregnancies with biparental genomic contribution
    Human Genetics, vol. 105, no. 1-2, pp. 112–115, 1999
23. Acceptance of prenatal diagnosis for genetic disorders in Lebanon
    Prenatal Diagnosis, vol. 19, no. 12, pp. 1109–1112, 1999
24. Familial complex chromosome rearrangement giving rise to balanced and unbalanced recombination products
    American Journal of Medical Genetics, vol. 79, no. 1, pp. 30–34, 1998
25. ACCEPTANCE OF FIRST-TRIMESTER PRENATAL DIAGNOSIS FOR THE HAEMOGLOBINOPATHIES IN LEBANON
    Prenatal Diagnosis, vol. 17, no. 5, pp. 423–428, 1997
26. Recurrent molar pregnancies in a family with extensive intermarriage: Report of a family and review of the literature
    Obstetrics & Gynecology, vol. 86, no. 4, pp. 692–695, 1995
27. Trisomy 22 and facioauriculovertebral (Goldenhar) sequence
    American Journal of Medical Genetics, vol. 46, no. 1, pp. 68–71, 1993
28. The application of automated metaphase scanning to direct preparations of chorionic villi
    Prenatal Diagnosis, vol. 9, no. 1, pp. 7–17, 1989
29. Cell cycle studies in chorionic villi
    Human Genetics, vol. 80, no. 2, pp. 127–134, 1988
30. Chromosome banding in direct preparations of chorionic villi
    Prenatal Diagnosis, vol. 8, no. 6, pp. 461–469, 1988