Published in Clin Genet on February 01, 1981
Phenotype-karyotype correlation in patients trisomic for various segments of chromosome 13. J Med Genet (1986) 1.23
Familial pericentric inversion (13) detected by antenatal diagnosis. J Med Genet (1984) 0.75
Molecular differential pathology of rhabdomyosarcoma. Genes Chromosomes Cancer (1989) 1.59
Radio-ulnar synostosis in Williams syndrome. A frequently associated anomaly. Pediatr Radiol (1991) 1.42
Clinical rubella with virus transmission to the fetus in a pregnant woman considered to be immune. N Engl J Med (1988) 1.19
Antibody tests in streptococcal pharyngitis. Streptozyme versus conventional methods. Clin Pediatr (Phila) (1973) 1.08
Chromosomal analysis of sixteen human rhabdomyosarcomas. Cancer Res (1988) 1.02
Increased serum hexosaminidase in a woman pregnant with fetus affected by mucolipidosis II (I-cell disease) N Engl J Med (1984) 1.01
Hepatitis B virus infection and liver disease in Ethiopian immigrants to Israel. Hepatology (1986) 1.01
Third report of t(19q)(13.4) in mesenchymal hamartoma of liver with comments on link to embryonal sarcoma. Pediatr Dev Pathol (1999) 1.01
Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridization. Hum Genet (1993) 0.98
Prenatal diagnosis of type-II glycogenosis. Lancet (1970) 0.98
Lethal neonatal multiorgan deficiency of carnitine palmitoyltransferase II. N Engl J Med (1991) 0.96
Chromosome analysis of 31 Wilms' tumors. Cancer Res (1990) 0.96
Health profile of Ethiopian immigrants in Israel: an overview. Isr J Med Sci (1993) 0.92
Pathologic features of the eye in trisomy 9. J Pediatr Ophthalmol Strabismus (1982) 0.91
Profound carnitine palmitoyltransferase II deficiency. J Pediatr (1994) 0.91
Terminal long-arm deletion of chromosome 1 in a male infant. Hum Genet (1979) 0.88
Structural analysis of hepatitis B surface antigen by monoclonal antibodies. J Clin Invest (1985) 0.88
[Bisalbuminemia induced by large doses of penicillins]. Harefuah (1981) 0.88
Rapid prenatal diagnosis of glycogen-storage disease type II by electron microscopy of uncultured amniotic-fluid cells. N Engl J Med (1984) 0.88
Karyotype studies in 18 ependymomas with literature review of 107 cases. Cancer Genet Cytogenet (1999) 0.86
Evidence for the existence of circulating monoclonal B-lymphocytes in multiple myeloma patients. Exp Hematol (1990) 0.84
Fetal mucolipidosis II (I-cell disease): radiologic and pathologic correlation. Pediatr Radiol (1986) 0.84
Partial trisomy 20p: familial occurrence. Am J Med Genet (2000) 0.84
Metacarpophalangeal pattern profile analysis in Sotos syndrome. Am J Med Genet (1985) 0.83
Hepatoblastoma in a child with trisomy 18: cytogenetics, liver anomalies, and literature review. Pediatr Pathol Lab Med (1997) 0.82
Cardiovascular abnormalities in children with fragile X syndrome. Pediatrics (1993) 0.82
Supernumerary chromosome marker (1) in a developmentally delayed child. Am J Med Genet (1995) 0.82
Adrenal carcinoma in child with history of fetal alcohol syndrome. Lancet (1977) 0.82
Further observations of ocular pathology in trisomy 9. J Pediatr Ophthalmol Strabismus (1989) 0.80
Deletion of (11)(q24.2) in a mother and daughter with similar phenotypes. Am J Med Genet (1994) 0.80
Epidemiology of rubella and congenital rubella infection in Israel, a country with a selective immunization program. Rev Infect Dis (1985) 0.80
Fragile X syndrome: recognition in young children. Pediatrics (1989) 0.79
A study of Salmonella O antigens by Ouchterlony's agar diffusion method. Isr J Med Sci (1968) 0.79
Growth patterns of human neuroblastoma xenografts and their relationship to treatment outcome. Cancer (1993) 0.79
Ocular abnormality associated with extra small autosome. Am J Ophthalmol (1968) 0.79
Physical mapping of the uterine leiomyoma t(12;14)(q13-15;q24.1) breakpoint on chromosome 14 between SPTB and D14S77. Genes Chromosomes Cancer (1994) 0.79
Chromosome changes in embryos treated with various teratogens. J Embryol Exp Morphol (1967) 0.78
Treatment related observations in solid tissues, fibroblast cultured and amniotic fluid cells of type II glycogenosis, Hurler disease and metachromatic leukodystrophy. Birth Defects Orig Artic Ser (1973) 0.78
Chromosomes in cleft-palate tissues. Lancet (1966) 0.78
A study of the O and protein antigens of Salmonella adelaide and Escherichia coli 0111:B4 by agar diffusion techniques. Isr J Med Sci (1972) 0.78
Bone marrow biopsy in multiple myeloma: a clinical pathological study. Isr J Med Sci (1988) 0.77
[Specific IgE for Schistosoma mansoni in Ethiopian immigrants]. Harefuah (1987) 0.77
The diagnostic reliability of anti-endomysial antibody in celiac disease: the north Israel experience. Isr J Med Sci (1995) 0.77
A new surgical procedure for correction of lip deformity in cranio-carpo-tarsal dysplasia (whistling face syndrome). J Oral Surg (1979) 0.77
Marker chromosome 21 identified by microdissection and FISH. Am J Med Genet (1995) 0.77
Bisalbuminaemia in pancreatic ascites. Postgrad Med J (1986) 0.75
Antenatal diagnosis of mucopolysaccharidosis type I (Hurler's disease) is not possible by electron microscopy of uncultured amniotic fluid cells. J Med Genet (1984) 0.75
Rubella antibodies in women of childbearing age during an epidemic and the two years thereafter. Isr J Med Sci (1976) 0.75
Pathologic features of the eye in triploidy. J Pediatr Ophthalmol Strabismus (1981) 0.75
Prenatal detection of triploidy. J Pediatr (1988) 0.75
Immunologic, morphologic and chromosomal characterization of a cell line (TC78) established from a child with acute lymphoblastic leukemia. Leuk Res (1985) 0.75
Early results of an extensive rubella epidemic. Int J Epidemiol (1975) 0.75
Plasma fibronectin levels in patients with coronary artery disease. Isr J Med Sci (1994) 0.75
[Developmental changes in the aorta, pulmonary artery and ductus arteriosus during the perinatal period]. Cesk Pediatr (1979) 0.75
Wilms tumor: summary of 54 cytogenetic analyses. Cancer Genet Cytogenet (1997) 0.75
Prenatal diagnosis of trisomy 20 by chorionic villus sampling (CVS): a case report with long-term outcome. Prenat Diagn (2001) 0.75
Arachnodactyly (Marfan's syndrome) with XYY karyotype. Am J Dis Child (1972) 0.75
Chromosome analyses in a rhabdoid tumor of the brain. Cancer Genet Cytogenet (1997) 0.75
A case of atypical Down's syndrome with mosaic 46,XX/46,XX-21+t(21q21q). Clin Genet (1976) 0.75
[Hemoglobin C in an Arab family]. Harefuah (1976) 0.75
Anti-Tja, a rare human isoantibody. First finding in Israel. Isr J Med Sci (1969) 0.75
Success and failure of a rubella immunization programme. Dev Biol Stand (1979) 0.75
Ocular findings associated with ring B chromosome. Am J Ophthalmol (1974) 0.75
Pediatric manpower needs in the area of developmental disorders and other chronic handicapping conditions. Appl Res Ment Retard (1985) 0.75
S-cells from a highly N-myc-amplified neuroblastoma are tumorigenic in nude mice. Anticancer Res (1994) 0.75
Excretion of urinary protein induced by extracorporeal piezoelectric lithotripsy. Br J Urol (1990) 0.75
Identification of the sex chromosomes in the bald eagle. Can J Genet Cytol (1975) 0.75
Linear nevi, hemihypertrophy, connective tissue hamartomas, and unusual neoplasms in children. J Pediatr (1987) 0.75
Plasma fibronectin levels in various clinical conditions. Isr J Med Sci (1985) 0.75
Uncombable-hair syndrome. Pediatr Dermatol (1987) 0.75
Comparison of chromosome analysis to DNA content by flow cytometry for pediatric tumors. Pediatr Pathol (1990) 0.75
Detection of unexpected clones of monosomy 7 in childhood acute lymphoblastic leukemia using fluorescence in situ hybridization. Anticancer Res (1994) 0.75
Familial partial duplication (1)(p21p31). Am J Med Genet (1995) 0.75
Monocyte suppressor function in burns: T cell-monocyte interaction in mediating suppression. Immunol Lett (1985) 0.75
Rubella immunity measured by hemagglutination inhibition and enzyme-linked immunosorbent assay. Isr J Med Sci (1985) 0.75