Published in Am J Hum Genet on May 01, 1975
The economics of clinical genetics services. II. A time analysis of a medical genetics clinic. Am J Hum Genet (1987) 1.49
Health care and disease prevention through genetic counseling: a regional approach. Am J Public Health (1976) 1.37
The economics of clinical genetics services. I. Preview. Am J Hum Genet (1987) 1.32
Genetic counseling. An evaluation of public health genetic clinics. West J Med (1976) 0.80
The Alberta Hereditary Diseases Program: a regional model for delivery of genetic services. CMAJ (1990) 0.76
Using Public-Private Partnerships to Mitigate Disparities in Access to Genetic Services: Lessons from Wisconsin. Adv Med Sociol (2016) 0.75
Genetic counseling. Am J Hum Genet (1974) 4.86
Who should do genetic counseling, and under what circumstances? Birth Defects Orig Artic Ser (1973) 1.23
Research in delivery of female health care. What shall be the role of the university department of obstetrics and gynecology? Am J Obstet Gynecol (1971) 1.04
Satellite clinics for tuberculosis care. Nurs Outlook (1972) 1.01
Codon selection in yeast. J Biol Chem (1982) 19.13
Sequence of the gene for iso-1-cytochrome c in Saccharomyces cerevisiae. Cell (1979) 10.86
Nucleotide sequence of a mutant eukaryotic gene: the yeast tyrosine-inserting ochre suppressor SUP4-o. Proc Natl Acad Sci U S A (1977) 10.64
The primary structure of the Saccharomyces cerevisiae gene for alcohol dehydrogenase. J Biol Chem (1982) 7.03
Deletion mapping of sequences essential for in vivo transcription of the iso-1-cytochrome c gene. Proc Natl Acad Sci U S A (1981) 6.26
The sequence of the DNAs coding for the mating-type loci of Saccharomyces cerevisiae. Cell (1981) 5.23
A position effect in the control of transcription at yeast mating type loci. Nature (1981) 5.23
Phylogenetic relationships among ascomycetes: evidence from an RNA polymerse II subunit. Mol Biol Evol (1999) 4.83
Mutation of a heterothallic strain to homothallism. Genetics (1975) 4.09
Macromolecule synthesis and breakdown in relation to sporulation and meiosis in yeast. J Bacteriol (1974) 4.07
Transcriptional regulation of the yeast cytochrome c gene. Proc Natl Acad Sci U S A (1979) 3.85
Synthesis and assembly of hepatitis B virus surface antigen particles in yeast. Nature (1982) 3.82
Isolation and sequence of the gene for iso-2-cytochrome c in Saccharomyces cerevisiae. Proc Natl Acad Sci U S A (1980) 3.62
A Polymorphism* in the 5' flanking region of the CD14 gene is associated with circulating soluble CD14 levels and with total serum immunoglobulin E. Am J Respir Cell Mol Biol (1999) 3.42
Identification and isolation of the yeast cytochrome c gene. Cell (1978) 3.39
CHARGE association: an update and review for the primary pediatrician. Clin Pediatr (Phila) (1998) 3.33
Identification of the yeast DNA sequences that correspond to specific tyrosine-inserting nonsense suppressor loci. J Mol Biol (1979) 3.29
Mutations of the yeast SUP4 tRNATyr locus: transcription of the mutant genes in vitro. Cell (1980) 3.24
Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome. Am J Hum Genet (2000) 3.16
Isolation and characterization of non-defective transducing elements of bacteriophage phi-80. Virology (1967) 3.15
In vitro mutation analysis of the mating-type locus in yeast. Cell (1981) 3.09
Choanal atresia and associated multiple anomalies. J Pediatr (1979) 2.98
Older paternal age and fresh gene mutation: data on additional disorders. J Pediatr (1975) 2.97
A cluster of seven tightly linked polymorphisms in the IL-13 gene is associated with total serum IgE levels in three populations of white children. J Allergy Clin Immunol (2000) 2.68
Effects of tRNATyr point mutations on the binding of yeast RNA polymerase III transcription factor C. J Biol Chem (1986) 2.55
The amniotic band disruption complex: timing of amniotic rupture and variable spectra of consequent defects. J Pediatr (1979) 2.46
Expression of a human gene for interferon in yeast. Nature (1981) 2.46
Transcription in yeast: separation and properties of multiple FNA polymerases. Proc Natl Acad Sci U S A (1972) 2.45
Cloning of the yeast tyrosine transfer RNA genes in bacteriophage lambda. J Mol Biol (1979) 2.44
Mating type and sporulation in yeast. I. Mutations which alter mating-type control over sporulation. Genetics (1975) 2.41
Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosome. J Mol Biol (1985) 2.39
Isolation of a gene from Drosophila by complementation in yeast. Nature (1981) 2.30
The primary structure of the alcohol dehydrogenase gene from the fission yeast Schizosaccharomyces pombe. J Biol Chem (1983) 2.29
Incidence of fibrocystic disease in Wessex. J Med Genet (1968) 2.22
Transcription initiation of eucaryotic transfer RNA genes. Cell (1982) 2.18
Successful repair in utero of a fetal diaphragmatic hernia after removal of herniated viscera from the left thorax. N Engl J Med (1990) 2.17
THE OCCURRENCE OF NATURAL DNA-RNA COMPLEXES IN E. COLI INFECTED WITH T2. Proc Natl Acad Sci U S A (1961) 2.12
Prenatal diagnosis of alpha-thalassemia. Clinical application of molecular hybridization. N Engl J Med (1976) 2.10
Yeast cytochrome c messenger RNA. In vitro translation and specific immunoprecipitation of the CYC1 gene product. J Biol Chem (1976) 2.07
Mutations at the yeast SUP4 tRNATyr locus: DNA sequence changes in mutants lacking suppressor activity. Cell (1980) 2.04
Isolation of the structural gene for alcohol dehydrogenase by genetic complementation in yeast. Nature (1980) 2.03
A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies. J Pediatr (1973) 1.98
Fetal surgery for congenital hydronephrosis. N Engl J Med (1982) 1.94
An in vitro RNA polymerase III system from S. cerevisiae: effects of deletions and point mutations upon SUP4 gene transcription. Nucleic Acids Res (1982) 1.93
The promoter sequence of a yeast tRNAtyr gene. Cell (1983) 1.91
Only one of two closely related yeast suppressor tRNA genes contains an intervening sequence. Nature (1981) 1.87
Effects of alterations in the 3' flanking sequence on in vivo and in vitro expression of the yeast SUP4-o tRNATyr gene. EMBO J (1985) 1.87
International, collaborative experience of 1789 patients having multifetal pregnancy reduction: a plateauing of risks and outcomes. J Soc Gynecol Investig (1996) 1.87
Penetrance and variability in neurofibromatosis: a genetic study of 60 families. Birth Defects Orig Artic Ser (1979) 1.85
Femoral hypoplasia--unusual facies syndrome. J Pediatr (1975) 1.84
Xylose isomerase from Escherichia coli. Characterization of the protein and the structural gene. J Biol Chem (1984) 1.82
Management of the fetus with congenital hydronephrosis. J Pediatr Surg (1982) 1.79
The OEIS complex (omphalocele, exstrophy, imperforate anus, spinal defects). Birth Defects Orig Artic Ser (1978) 1.79
The safety and efficacy of chorionic villus sampling for early prenatal diagnosis of cytogenetic abnormalities. N Engl J Med (1989) 1.79
Prenatal diagnosis of beta-thalassaemia and sickle-cell anaemia. Experience with 24 cases. Lancet (1977) 1.77
Meier-Gorlin syndrome: report of eight additional cases and review. Am J Med Genet (2001) 1.76
The Marfan syndrome locus: confirmation of assignment to chromosome 15 and identification of tightly linked markers at 15q15-q21.3. Genomics (1991) 1.75
Costello syndrome: phenotype, natural history, differential diagnosis, and possible cause. J Pediatr (1998) 1.74
Fetal hydrops and death from sacrococcygeal teratoma: rationale for fetal surgery. Am J Obstet Gynecol (1989) 1.74
Structural features of yeast tRNA genes which affect transcription factor binding. EMBO J (1984) 1.73
Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease. Am J Hum Genet (1996) 1.70
Physical analysis of the CYC1-sup4 interval in Saccharomyces cerevisiae. Mol Cell Biol (1981) 1.68
Genetic analysis of the processing of a spliced tRNA. EMBO J (1982) 1.67
Glucose-6-phosphatase deficiency caused by radiation-induced alleles at the albino locus in the mouse. Proc Natl Acad Sci U S A (1968) 1.64
Demonstration in mouse of X-ray induced deletions for a know enzyme structural locus. Nature (1974) 1.63
Stimulus coding in topographic and nontopographic afferent modalities: on the significance of the activity of individual sensory neurons. Psychol Rev (1968) 1.60
Molecular analysis of an unbalanced deletion of the short arm of chromosome 5 that produces no phenotype. Am J Hum Genet (1986) 1.59
Structure of the Schizosaccharomyces pombe cytochrome c gene. Mol Cell Biol (1982) 1.58
Physical analysis of mating-type loci in Saccharomyces cerevisiae. Cold Spring Harb Symp Quant Biol (1981) 1.58
Transforming activity in single-stranded DNA from Bacillus subtilis. J Mol Biol (1968) 1.57
First-trimester aneuploidy screening using serum human chorionic gonadotropin (hCG), free ahCG, and progesterone. Prenat Diagn (1991) 1.56
Prader-Willi syndrome. A resumé of 32 cases including an instance of affected first cousins, one of whom is of normal stature and intelligence. J Pediatr (1972) 1.55
Prenatal diagnosis of hemoglobin H disease. J Pediatr (1978) 1.55
Mating type and sporulation in yeast. II. Meiosis, recombination, and radiation sensitivity in an alpha-alpha diploid with altered sporulation control. Genetics (1975) 1.54
Gene size differentially affects the binding of yeast transcription factor tau to two intragenic regions. Proc Natl Acad Sci U S A (1987) 1.53
Prenatal genetic diagnosis in 3000 amniocenteses. N Engl J Med (1979) 1.50
Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy. Am J Hum Genet (1992) 1.50
Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome. Nat Genet (1996) 1.49
Rapid determination of fetal sex by deoxyribonucleic acid amplification of Y chromosome-specific sequences. Am J Obstet Gynecol (1989) 1.46
Diagnosis of homozygous alpha-thalassemia in cultured amniotic-fluid fibroblasts. N Engl J Med (1978) 1.46
Second-trimester maternal serum alpha-fetoprotein levels and the risk of subsequent fetal death. N Engl J Med (1991) 1.45
Cyclodextrins in the treatment of a mouse model of Niemann-Pick C disease. Life Sci (2001) 1.45
Molecular characterisation of the tyrosine tRNA genes of yeast. Nature (1977) 1.44
The T-locus of the mouse: implications for mechanisms of development. Curr Top Dev Biol (1970) 1.43
Re-evaluation of new X-linked syndrome for evidence of CHARGE syndrome or association. Am J Med Genet (1989) 1.43
A randomized comparison of transcervical and transabdominal chorionic-villus sampling. The U.S. National Institute of Child Health and Human Development Chorionic-Villus Sampling and Amniocentesis Study Group. N Engl J Med (1992) 1.43
Level of tryptophan messenger RNA in Escherichia coli. J Mol Biol (1968) 1.43
The origin of red algae: implications for plastid evolution. Proc Natl Acad Sci U S A (1997) 1.42
Transcription in yeast: alpha-amanitin sensitivity and other properties which distinguish between RNA polymerases I and III. Proc Natl Acad Sci U S A (1976) 1.42
Detection of aneuploidy involving chromosomes 13, 18, or 21, by fluorescence in situ hybridization (FISH) to interphase and metaphase amniocytes. Am J Hum Genet (1991) 1.41
Importance of the forest canopy to fluxes of methyl mercury and total mercury to boreal ecosystems. Environ Sci Technol (2001) 1.41
The antenatal detection of genetic disorders. Current status and future prospects. Obstet Gynecol (1976) 1.39
Macrocephaly-cutis marmorata telangiectatica congenita: a distinct disorder with developmental delay and connective tissue abnormalities. Am J Med Genet (1997) 1.38
Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombination. Hum Mol Genet (2001) 1.38
In utero treatment of urinary tract obstruction. Am J Obstet Gynecol (1982) 1.36
Chorionic villus sampling: experience of the first 1000 cases. Am J Obstet Gynecol (1986) 1.36
Deletion from the long arm of chromosome 4 (46,XX,4q-) associated with congenital anomalies. J Med Genet (1973) 1.36
Confirmation of the Cohen syndrome. J Pediatr (1978) 1.35
Cytogenetic results from the U.S. Collaborative Study on CVS. Prenat Diagn (1992) 1.35