Published in Am Rev Respir Dis on September 01, 1968
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Genetic counseling of asymptomatic carriers in a primary care setting. The effectiveness of screening and counseling for beta-thalassemia trait. Ann Intern Med (1986) 0.94
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Multipotent human hematopoietic cell line K562: lineage-specific constitutive and inducible antigens. Leuk Res (1987) 0.88
The neurofibroma in von Recklinghausen neurofibromatosis has a unicellular origin. Am J Hum Genet (1991) 0.86
Protein synthesis in reticulocytes maturing in vivo. Nature (1965) 0.86
Newborn screening for sicle-cell disease. Benefits and burdens. N Y State J Med (1978) 0.86
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Erythroleukemia manifesting delta beta-thalassemia. Hemoglobin (1983) 0.85
Pathogenesis of deficient serum alpha1-antitrypsin in the type ZZ homozygote. Biochem Genet (1974) 0.85
An adult homozygous for persistent fetal hemoglobin. Ann Intern Med (1970) 0.85
Alveolar cell carcinoma in identical twins. Similarity in time of onset, histochemistry, and site of metastasis. Ann Intern Med (1977) 0.85
The diagnosis of beta-thalassemia trait: a review. Am J Hematol (1976) 0.84
Regulation of K562 cell transferrin receptors by exogenous iron. J Cell Physiol (1985) 0.84
Linkage between the MN- and Hb beta-loci? Hum Hered (1972) 0.84
A Lepore hemoglobin in a Rumanian family. Hum Hered (1969) 0.84
Toward providing parents the option of avoiding the birth of the first child with Cooley's anemia: response to hemoglobinopathy screening and counseling during pregnancy. Ann N Y Acad Sci (1985) 0.84
Sickle hemoglobin: a specific radioimmunoassay. Blood (1974) 0.84
Incorporation of screening and genetic counseling for beta-thalassemia trait into primary health care: effects on knowledge and attitudes. Birth Defects Orig Artic Ser (1982) 0.83
Acquired hemoglobin H disease in idiopathic myelofibrosis. Am J Hematol (1979) 0.82
K562 human erythroleukemia cells demonstrate commitment. Blood (1985) 0.81
K562 human leukemia cell passages differ in embryonic globin gene expression. Leuk Res (1984) 0.81
Solubilization of a reticulocyte ribosomal fraction responsible for the decline in ribosomal activity with cell maturation. Arch Biochem Biophys (1971) 0.81
Induction of megakaryocytic characteristics in human leukemic cell line K562: polyploidy, inducers, and secretion of mitogenic activity. J Biol Regul Homeost Agents (1988) 0.80
Oncogene expression in neurofibromatosis. Ann N Y Acad Sci (1986) 0.80
The linkage relationships of the haemoglobin beta, delta and alpha loci with 34 genetic marker systems. Ann Hum Genet (1977) 0.80
Predicting immediate outcome of genetic counseling following screening. Soc Biol (1979) 0.80
Thallium-201 scintigraphy in diagnosis of coronary stenosis. Comparison with electrocardiography and coronary arteriography. Br Heart J (1979) 0.79
Human lymphocyte telomerase is genetically regulated. Genes Chromosomes Cancer (1998) 0.79
Hemin preferentially stimulates synthesis of alpha-globin in K562 human erythroleukemia cells. Blood (1982) 0.79
High resolution analysis of hemoglobins: polyacrylamide isoelectric focusing. Biochem Med (1972) 0.79
Telomere-related components are coordinately synthesized during human T-lymphocyte activation. Leuk Res (1999) 0.79
Tumor suppressor genes and inherited predisposition to malignancy. Semin Oncol (1989) 0.78
Serm alpha-antitrypsin types: elastase inhibition versus trypsin inhibition. Hum Hered (1974) 0.78
Renal cortical imaging in 35 patients: superior quality with 99mTc-DMSA. J Nucl Med (1974) 0.77
Unpredictable error in calculated bicarbonate homeostasis during pediatric intensive care: the delusion of fixed pK'. Clin Chem (1983) 0.77
Demonstration of commitment by K562 human erythroleukemia cells. Prog Clin Biol Res (1985) 0.77
Cell cycle-dependent surface changes in Chinese hamster cells grown in suspension culture. Exp Cell Res (1975) 0.77
Hereditary haemorrhagic telangiectasia: aggravation by oral contraceptives? Lancet (1970) 0.77
Serum antitrypsin synthesis by the isolated perfused rat liver. Proc Soc Exp Biol Med (1975) 0.77
Induction of HL60 cell differentiation by tiazofurin and its analogues: characterization and efficacy. Blood (1991) 0.77
Computerised graphic representation of clinical chemistry results. J Clin Pathol (1981) 0.77
Disappearance of ribosomes and polyribosomes during in vivo erythroid maturation. Nature (1967) 0.77
Sickle beta-thalassemia: identical twins differing in severity implicate nongenetic factors influencing course. Am J Hematol (1976) 0.76
Regulation of the activity of heme degradative enzymes in K562 erythroleukemic cells: induction by thymidine. Exp Hematol (1987) 0.76
Confusion about breast-cancer screening. N Engl J Med (1997) 0.75
K562 human erythroleukemia cell variants resistant to growth inhibition by butyrate have deficient histone acetylation. Am J Hum Genet (1984) 0.75
Characteristics of the antitrypsin activity of human serum. J Clin Pathol (1973) 0.75
Prenatal screening for hemoglobinopathies. Am J Hum Genet (1991) 0.75
Genetics for the cardiologist. Part I: mendelian inheritance. Mod Concepts Cardiovasc Dis (1978) 0.75
Tetrahydrocannabinol inhibits adenyl cyclase in human leukemia cells. Life Sci (1990) 0.75
Single-cell analysis of the relationship among transferrin receptors, proliferation, and cell cycle phase in K562 cells. Cytometry (1985) 0.75
Genetic screening: whose responsibility? JAMA (1976) 0.75
Trypsin enhances erythropoiesis in vitro. J Lab Clin Med (1980) 0.75
Erythropoiesis in vitro: enhancement by neuraminidase. Blood (1981) 0.75
Textural differences between AA and SS blood specimens as detected by image analysis. Cytometry (1994) 0.75
Deleterious mutations of both BRCA1 and BRCA2 in three siblings. Genet Test (1998) 0.75
Induction of hemoglobin synthesis in K562 cells by carbon dioxide deficiency. Int J Cell Cloning (1987) 0.75
Sickle cell trait/hereditary persistence of fetal hemoglobin trait. Misdiagnosis as sickle cell anemia by newborn screening. Am J Dis Child (1979) 0.75
The contribution of red cell morphology to the diagnosis of beta-thalassemia trait. Blood Cells (1986) 0.75
Genetics for the cardiologist. Part II: Chromosomal and polygenic inheritance and genetic counseling. Mod Concepts Cardiovasc Dis (1978) 0.75
Genetic testing for breast-ovarian cancer susceptibility: a regional trial. Genet Test (1998) 0.75
Long survival in sickle-cell disease. Lancet (1973) 0.75
Genetic considerations in neuromuscular diseases. Adv Neurol (1977) 0.75
What you should know about chromosome analysis. Alaska Med (1969) 0.75
Erythroid differentiation of K562 cells: mixed colonies as an index of delayed expression of commitment. Exp Hematol (1987) 0.75
Amniotic fluid indicators of fetal maturity. Obstet Gynecol (1972) 0.75
The cytopathic effect of herpes simplex virus on HEp-2 cells as shown by scanning electron microscopy. J Gen Virol (1974) 0.75
Genetic counseling in medical practice. Alaska Med (1969) 0.75
Familial hearing loss associated with branchial fistulas. Pediatrics (1969) 0.75
No limits to genetic inquiry. Hastings Cent Rep (1988) 0.75
Enhanced polyribosome recovery from reticulocytes using heparin. Exp Cell Res (1967) 0.75
Oncogene expression in myelopoiesis. Int J Cell Cloning (1987) 0.75
Hypersplenic thrombocytopenia in sickle cell-bata thalassemia. Am J Med Sci (1972) 0.75
Chronic phase lipids in sera of chronic fatigue syndrome (CFS), chronic ciguatera fish poisoning (CCFP), hepatitis B, and cancer with antigenic epitope resembling ciguatoxin, as assessed with MAb-CTX. J Clin Lab Anal (2003) 0.75
Assessment of evaluation of hospitalized pediatric patients with genetic disorders. Clin Pediatr (Phila) (1981) 0.75
Issues in implementing prenatal screening for cystic fibrosis: results of a working conference. Genet Med (2001) 0.75