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O.S. Alfi

Observed names: O ALFI, O Alfi, O S Alfi, O. Alfi, O. S. Alfi, OMAR S. ALFI, Omar Alfi, Omar S. Alfi
OpenAlex ID: A5108570753
Optical studies of the interaction of 4?-6-diamidino-2-phenylindole with DNA and metaphase chromosomes
1977 · M. S. Lin, D. E. Comings, et al. · Chromosoma · 166
Deletion of the short arm of chromosome no.9 (46,9p-): a new deletion syndrome.
1973 · O Alfi, G N Donnell, et al. · PubMed · 141
Autologous Hematopoietic Stem Cell Transplantation in 48 Patients with End-Stage Chronic Liver Diseases
2010 · Hosny Salama, Abdel-Rahman Zekri, et al. · Cell Transplantation · 122
Evidence for genetic control of nondisjunction in man.
1980 · O S Alfi, R Chang, et al. · PubMed · 120
Detection of sister chromatid exchanges by 4?-6-diamidino-2-phenylindole fluorescence
1976 · M. S. Lin, O. S. Alfi · Chromosoma · 70
The use of color doppler ultrasound to identify fetuses at increased risk for trisomy 21: An alternative for high-risk patients who decline genetic amniocentesis
1995 · G DEVORE, O ALFI · Obstetrics and Gynecology · 69
The 9p- syndrome.
1976 · O S Alfi, G N Donnell, et al. · PubMed · 45
The prenatal detection of the fragile X chromosome: Review of recent experience
1986 · Edmund C. Jenkins, W. Ted Brown, et al. · American Journal of Medical Genetics · 33
The association between an abnormal nuchal skin fold, trisomy 21, and ultrasound abnormalities identified during the second trimester of pregnancy
1993 · G. R. DeVore, O. Alfi · Ultrasound in Obstetrics and Gynecology · 29
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Partial Trisomy of the Long Arm of Chromosome No. 7
1973 · Omar S. Alfi, George N. Donnell, et al. · Journal of Medical Genetics · 27
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Role of amniocentesis in ultrasound-detected fetal malformations.
1986 · L D Platt, G R DeVore, et al. · PubMed · 25
Double Autosomal Trisomy and Mosaicism for Chromosomes No. 8 and No. 21
1974 · Miriam G. Wilson, Atsuko Fujimoto, et al. · Journal of Medical Genetics · 21
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Differential Fluorescence of Sister Chromatids With 4′-6-diamidino-2-phenylindole
1976 · M. S. Lin, O. S. Alfi, et al. · Canadian Journal of Genetics and Cytology · 20
HPLC analysis of uridine diphosphate sugars: decreased concentrations of uridine diphosphate galactose in erythrocytes and cultured skin fibroblasts from classical galactosemia patients
1995 · Yan-Kang Xu, Francine R. Kaufman, et al. · Clinica Chimica Acta · 18
Ambiguous Genitalia in XX Male Children: Report of Two Infants
1977 · Thomas F. Roe, Omar S. Alfi · PEDIATRICS · 18
Trisomy 19 q.
1976 · M Lange, O S Alfi · PubMed · 17
Trisomy 22: a clinically identifiable syndrome.
1975 · O S Alfi, R G Sanger, et al. · PubMed · 16
Fucosidosis: Clinical, Pathologic, and Biochemical Studies of Five Patients
1976 · Benjamin H. Landing, George N. Donnell, et al. · Advances in experimental medicine and biology · 13
46, Del (9) (22:), a new deletion syndrome.
1974 · O S Alfi, R G Sanger, et al. · PubMed · 11
Regional mapping of the gene for human UDPGal 4-epimerase on chromosome 1 in mouse-human hybrids
2008 · M.S. Lin, J. Oizumi, et al. · Cytogenetics and Cell Genetics · 10
Variation in lateral asymmetry of human chromosome 1
2008 · M.S. Lin, O.S. Alfi · Cytogenetics and Cell Genetics · 10
Quinacrine Fluoromicroscopy in the Identification of Human Mitotic Chromosomes
1971 · Omar S. Alfi, George N. Donnell, et al. · PEDIATRICS · 10
Medical genetics for the otorhinolaryngologist
1980 · George N. Donnell, Omar S. Alfi · The Laryngoscope · 9
Performing cytogenetic studies on ascitic, amniotic and hygroma fluid.
1990 · L D Platt, G R DeVore, et al. · PubMed · 8
False-positive amniotic fluid acetylcholinesterase results: the need for a multifacet approach to the prenatal diagnosis of neural tube defects.
1985 · J E Lee, W G Ng, et al. · PubMed · 7
Works count: 50
Citation count: 1,093
H-index: 16
I10-index: 22
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