"Ashkenazi Jewish"

Key Phrases: New York, Ashkenazi Jewish, Dor Yeshorim, Ashkenazi Jews, French Canadians, Academic Press All, acetylhexosaminidase component, second most common mutation, substrate deprivation therapy, human hexosaminidase, arrested cerebral development, ganglioside catabolism (see more)

Key Phrases: New York, Ashkenazi Jewish, Dor Yeshorim, Ashkenazi Jews, French Canadians, Academic Press All, National Institutes of Health, San Diego, Bernard Sachs, Moroccan Jews, United States, Frameshift Acute, Ashkenazi Tay-Sachs, Mount Sinai Hospital, Dos Santos, Hex A-deficient, Acta Neuropathol, Eastern Europe, Tay Sachs, Los Angeles, Moroccan Jewish, Puerto Rican, Ashkenazic Jews, Central Europe, Pennsylvania Dutch, acetylhexosaminidase component, second most common mutation, substrate deprivation therapy, human hexosaminidase, arrested cerebral development, ganglioside catabolism, amaurotic family idiocy, infantile amaurotic idiocy, altered splice site, prenatal carrier screening, hexosaminidase isoenzymes, intron placement, acid sphingomyelinase gene, cerebral lipidoses, pseudodeficiency allele, splice junction mutation, ganglioside storage, faulty association, hexosaminidase activity, severe subacute, ganglioside metabolism, membranous cytoplasmic bodies, heterozygote screening, neurologic phenotype, generalized gangliosidosis (see less)

Key Phrases: Biol Chem, Clin Invest, Hum Genet, Proc Natl Acad Sci, New York, Clin Endocrinol Metab, Med Genet, Cell Biol, Biol Client, Nat Genet, Biochim Biophys Acta, Pediatr Res (see more)

Key Phrases: Biol Chem, Clin Invest, Hum Genet, Proc Natl Acad Sci, New York, Clin Endocrinol Metab, Med Genet, Cell Biol, Biol Client, Nat Genet, Biochim Biophys Acta, Pediatr Res, Inherit Metab Dis, Exp Med, Thromb Haemost, Biochem Biophys Res Commun, Proc Nail Acad Sci, Arch Dis Child, Clin Genet, Hum Mol Genet, United States, Clin Chim Acta, Lab Clin Med, Ann Intern Med, Hum Mutat (see less)

Key Phrases: Natl Cancer Inst, New Engl, Hum Genet, Ashkenazi Jewish, Cancer Res, United States, risk assessment clinic, following subcutaneous mastectomy, cancer risk counseling, male breast cancer patients, breast cancer onset, final assessment category (see more)

Key Phrases: Natl Cancer Inst, New Engl, Hum Genet, Ashkenazi Jewish, Cancer Res, United States, Nature Genet, New York, Clin Oncol, Obstet Gynecol, Breast Cancer Linkage Consortium, Health Psychol, Cancer Causes Control, Lahey Clinic, Nucl Med, American Cancer Society, Cancer Epidemiol Biomark Prev, American College of Radiology, Ann Intern Med, Ashkenazi Jews, Plast Reconstr Surg, Collaborative Group, Prev Med, Gynecol Oncol, Health Study, risk assessment clinic, following subcutaneous mastectomy, cancer risk counseling, male breast cancer patients, breast cancer onset, final assessment category, familial ovarian cancer registry, dense glandular tissue, sporadic ovarian cancers, stereotaxic core biopsy, breast cancer risk assessment, primary peritoneal carcinoma, hereditary ovarian cancer, prophylactic mastectomy, prophylactic oophorectomy, raloxifene groups, serous histology, stereotaxic biopsy, hereditary cancer syndromes, nonpalpable breast lesions, ovarian cancer families, borderline tumors, penetrance estimates, women taking placebo, mutation carriers (see less)

Key Phrases: Hum Genet, Proc Natl Acad Sci, Cell Biol, Biol Chem, Med Genet, New York, functional nullisomy, liver phosphorylase kinase deficiency, lactase phenotypes, galactitol excretion, hypermutable site, endometrial intraepithelial carcinoma (see more)

Key Phrases: Hum Genet, Proc Natl Acad Sci, Cell Biol, Biol Chem, Med Genet, New York, Clin Invest, Nature Genet, Hum Mol Genet, United States, Genes Dev, Clin Endocrinol Metab, Nucleic Acids Res, Cancer Genet Cytogenet, Clin Oncol, Inherit Metab Dis, Pediatr Res, Natl Cancer Inst, Biochim Biophys Acta, Trends Genet, Biochem Biophys Res Commun, Ashkenazi Jewish, Exp Med, Genome Res, Location Symbol Status Locus Name, functional nullisomy, liver phosphorylase kinase deficiency, lactase phenotypes, galactitol excretion, hypermutable site, endometrial intraepithelial carcinoma, intestinal microvillar proteins, glycogen debranching enzyme gene, insulin action pathway, mature lactase, glucagon receptor gene, familial pancreatic cancer, general insertion site, muscle glycogenoses, patients with hereditary fructose intolerance, severe generalized hypotonia, tyrosinosis type, gluconeogenesis defects, pyrophosphorylase pathway, sucraseisomaltase deficiency, heartbeat disorders, essential pentosuria, cosmid contig containing, desmoplastic small round cell tumor, respiratory chain disorders (see less)