Published in Clin Genet on March 01, 1979
Maternal serum alpha-fetoprotein screening and fetal chromosome anomalies: is lowering maternal age for amniocentesis preferable? Am J Med Genet (1992) 2.78
Synergistic interaction of p185c-neu and the EGF receptor leads to transformation of rodent fibroblasts. Cell (1989) 2.30
The 13q-deletion syndrome. Am J Hum Genet (1969) 2.06
Degree of inhibition of cortical acetylcholinesterase activity and cognitive effects by donepezil treatment in Alzheimer's disease. J Neurol Neurosurg Psychiatry (2005) 1.89
Cognitive correlates of cortical cholinergic denervation in Parkinson's disease and parkinsonian dementia. J Neurol (2005) 1.65
Paternal trisomy 21 mosaicism and Down's syndrome. Am J Hum Genet (1971) 1.65
United States survey on chromosome mosaicism and pseudomosaicism in prenatal diagnosis. Prenat Diagn (1984) 1.57
Trisomy 22: a clinical entity. J Pediatr (1971) 1.55
The need for more accurate and timely diagnosis in Fanconi anemia: a report from the International Fanconi Anemia Registry. Pediatrics (1993) 1.51
The syndrome of ectrodactyly, ectodermal dysplasia and cleft lip and palate: report of a family demonstrating a dominant inheritance pattern. Clin Genet (1972) 1.42
Chromosomal polymorphisms of 1, 9, 16, and Y in 4 major ethnic groups: a large prenatal study. Am J Med Genet (1987) 1.41
Phenotypic features and impact of beta blocker or calcium antagonist therapy on aortic lumen size in the Marfan syndrome. Am J Cardiol (1999) 1.35
Immunofluorescent cell assay of neonatal calf diarrhea virus. Can J Comp Med (1975) 1.30
Familial translocation with partial trisomy of 13 and 22: evidence that specific regions of chromosomes 13 and 22 are responsible for the phenotype of each trisomy. J Med Genet (1977) 1.30
Trisomy 21 mosaicism in a woman with two children with trisomy 21 Down's syndrome. J Med Genet (1974) 1.29
A stable human dicentric chromosome, t dic (12;14)(p13;p13) including an intercalary satellite region between centromeres. Am J Hum Genet (1973) 1.26
Influence of nuclear selection criteria on sex chromatin frequency in oral mucosa cells of newborn females. Cytogenetics (1967) 1.25
Strategies for motivating Latino couples' participation in qualitative health research and their effects on sample construction. Am J Public Health (2001) 1.23
Radiation exposure and associated risks to operating-room personnel during use of fluoroscopic guidance for selected orthopaedic surgical procedures. J Bone Joint Surg Am (1983) 1.23
Characterization of a neu/c-erbB-2 protein-specific activating factor. Proc Natl Acad Sci U S A (1991) 1.21
Diagnosis of Fanconi anemia in patients without congenital malformations: an international Fanconi Anemia Registry Study. Am J Med Genet (1997) 1.20
Partial thyroxine-binding globulin deficiency in a family. Pediatrics (1969) 1.15
Evaluation of growth and hormonal status in patients referred to the International Fanconi Anemia Registry. Pediatrics (2001) 1.13
Leukemia in Fanconi's anemia: cytogenetic and tumor virus susceptibility studies. Blood (1970) 1.12
Branchio-oto-renal syndrome: reduced penetrance and variable expressivity in four generations of a large kindred. Am J Med Genet (1986) 1.11
A partial long arm deletion of chromosome 7:46,XY,del(7)(q32). J Med Genet (1977) 1.09
Familial de Lange syndrome. Report of three cases in a sibship. Clin Genet (1971) 1.09
Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies. Prenat Diagn (1992) 1.09
Familial x/x translocation: t(x;x)(p22;q13) Cytogenet Cell Genet (1974) 1.08
Expression of the neu proto-oncogene by Schwann cells during peripheral nerve development and Wallerian degeneration. J Neurosci Res (1992) 1.08
State-sponsored maternal serum alpha-fetoprotein activities: current issues in genetics and public health. Am J Hum Genet (1990) 1.07
XXXXY boy. A 15-month-old child with normal intellectual development. Am J Dis Child (1970) 1.06
Interstitial deletion of chromosome 2 (p23p25). Am J Med Genet (1987) 1.06
Serologic detection of a y-linked gene in xx males and xx true hermaphrodites. N Engl J Med (1976) 1.04
Absence of autophosphorylation site Y882 in the p185neu oncogene product correlates with a reduction of transforming potential. Oncogene (1998) 1.04
Thrombocytopenia in malaria. Southeast Asian J Trop Med Public Health (1992) 1.03
Fungus allergens inside and outside the residences of atopic and control children. Arch Environ Health (1995) 1.01
Paternal uniparental disomy for chromosome 1 revealed by molecular analysis of a patient with pycnodysostosis. Am J Hum Genet (1998) 1.01
Effect of three preservatives on the growth of Bacillus cereus, Vero cytotoxigenic Escherichia coli and Staphylococcus aureus, on plates with gradients of pH and sodium chloride concentration. Int J Food Microbiol (1993) 1.01
Trisomy 18 mosaicism in two siblings. Clin Genet (1974) 1.00
His-426 of the Pseudomonas aeruginosa exotoxin A is required for ADP-ribosylation of elongation factor II. Proc Natl Acad Sci U S A (1988) 0.99
Batch purification of ovomucoid and characterization of the purified product. Biochemistry (1971) 0.99
Bleeding peptic ulcer--risk factors for rebleeding and sequential changes in endoscopic findings. Gut (1994) 0.97
Genetic and clinical considerations of long-arm deletion of the X chromosome. Pediatrics (1970) 0.97
A liveborn case of 49,XXXY, + 18. J Med Genet (1980) 0.97
In vitro cytotoxicity of lymphocytes from patients with "acquired" and sex-linked agammaglobulinaemia. Clin Exp Immunol (1971) 0.97
Teaching hand hygiene to medical students using a hands-on approach. J Hosp Infect (2010) 0.96
Trans receptor inhibition of human glioblastoma cells by erbB family ectodomains. Proc Natl Acad Sci U S A (1997) 0.95
Brachmann-de Lange syndrome. Report of two cases in a sibship. Am J Dis Child (1973) 0.95
Identification of antibiotic-resistance-gene molecular signatures suitable as tracers of pristine river, urban, and agricultural sources. Environ Sci Technol (2010) 0.94
Incidence and significance of supernumerary marker chromosomes in prenatal diagnosis. Am J Hum Genet (1984) 0.93
Cytogenetics of fetal wastage. N Engl J Med (1975) 0.93
The role of distinct p185neu extracellular subdomains for dimerization with the epidermal growth factor (EGF) receptor and EGF-mediated signaling. Proc Natl Acad Sci U S A (2001) 0.93
Number of C-bands of human isochromosome Xqi and relation to 45,X mosaicism. J Med Genet (1978) 0.93
Fetal wastage and maternal mosaicism. Obstet Gynecol (1972) 0.93
Metabolism and disposition of 1-bromopropane in rats and mice following inhalation or intravenous administration. Toxicol Appl Pharmacol (2006) 0.92
Microbiological standards for foods. II. Lab Pract (1969) 0.92
Minute chromosomes replacing the Y chromosome carry Y-specific sequences by restriction fragment analysis and in situ hybridization. Am J Med Genet (1985) 0.92
Inhibition of a naturally occurring EGFR oncoprotein by the p185neu ectodomain: implications for subdomain contributions to receptor assembly. Oncogene (1998) 0.91
A rare case of 68,XX triploidy diagnosed by amniocentesis. Prenat Diagn (1989) 0.91
Home dampness and childhood respiratory symptoms in a subtropical climate. Arch Environ Health (1996) 0.90
Murine thioredoxin peroxidase delays neuronal apoptosis and is expressed in areas of the brain most susceptible to hypoxic and ischemic injury. DNA Cell Biol (1997) 0.90
Prenatal diagnosis of 45,X/46,XY mosaicism with postnatal confirmation in a phenotypically normal male infant. Clin Genet (1976) 0.89
The incidence of protrusio acetabuli in Marfan's syndrome and its relationship to bone mineral density. J Pediatr Orthop (2001) 0.89
Prenatal diagnosis of genetic disease. Life Sci (1974) 0.89
Parental mosaicism in trisomy 18. Pediatrics (1972) 0.89
Deceleration of intellectual development in a XXXXY child: a follow-up. Am J Dis Child (1971) 0.89
Mosaicism of an abnormally long B chromosome in a boy with physical and mental retardation. Pediatrics (1967) 0.89
Definition of the critical interval for Smith-Magenis syndrome. Cytogenet Cell Genet (1997) 0.88
T-cell depletion and autologous stem cell transplantation in the management of tumour stage mycosis fungoides with peripheral blood involvement. Br J Haematol (2001) 0.88
Separation and characterization of the ovoinhibitors from chicken egg white. Biochemistry (1969) 0.88
Population screening for hemochromatosis: the evolving role of genetic analysis. Ann Intern Med (1998) 0.88
Detection of an interstitial deletion of 2q21-22 by high resolution comparative genomic hybridization in a child with multiple congenital anomalies and an apparent balanced translocation. Am J Med Genet A (2004) 0.88
ST22 and ST239 MRSA duopoly in Singaporean hospitals: 2006-2010. Epidemiol Infect (2012) 0.88
Supernumerary small ring chromosome. J Med Genet (1977) 0.87
Airborne fungus allergen in association with residential characteristics in atopic and control children in a subtropical region. Arch Environ Health (1997) 0.86
47,XXY-48,XXXY-49,XXXXY mosaicism in a 4-year-old child. Am J Dis Child (1971) 0.86
Klinefelter's syndrome in identical twins with the 46,XX chromosome constitution. Am J Med (1972) 0.86
The use of amniocentesis for prenatal genetic counseling. Bull N Y Acad Med (1970) 0.86
Prenatal chromosome analysis. Nature (1970) 0.86
Hazards of amniocentesis: an unidentifiable fragment. Clin Genet (1978) 0.86
Problems in prenatal diagnosis resulting from chromosomal mosaicism. Clin Genet (1972) 0.85
Congenital deficiency of alpha-fetoprotein. Am J Obstet Gynecol (1992) 0.85
Response of agammaglobulinaemic lymphocytes in mixed lymphocyte culture. Clin Exp Immunol (1969) 0.85
Sustained meticillin-resistant Staphylococcus aureus control in a hyper-endemic tertiary acute care hospital with infrastructure challenges in Singapore. J Hosp Infect (2013) 0.85
Parental chromosomal aberrations associated with multiple abortions and an abnormal infant. Obstet Gynecol (1970) 0.84
Pitfalls in prenatal diagnosis resulting from chromosomal mosaicism. J Pediatr (1972) 0.84
Non-fluorescent and non-heterochromatic Y chromosome in 45, X 46,XY mosaicism. Ann Genet (1974) 0.84
A child with presumptive monosomy 21 (45,XY,-21) in a family in which some members are Gq-. Cytogenet Cell Genet (1976) 0.84
Determiniation of trypsin-inhibitor complex dissociation by use of the active site titrant, p-nitrophenyl p'-guanidinobenzoate. Biochemistry (1970) 0.83
A high incidence of maternal cell contamination of amniotic fluid cell cultures. Am J Med Genet (1983) 0.83
Methicillin-resistant Staphylococcus aureus infections. Taiwan Yi Xue Hui Za Zhi (1988) 0.83
Sequence selective coordination of Mg2+(aq) to DNA. J Inorg Biochem (1993) 0.83