K. Smith

发表

Isolation and characterization of cloned human DNA fragments carrying reiterated sequences common to both autosomes and the X chromosome.

H. Willard, B. Schmeckpeper, K. Smith, 1981, Nucleic acids research.

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.

L. Kunkel, S. Wachtel, W. R. Breg, 1977, Proceedings of the National Academy of Sciences of the United States of America.

Characterization and evolution of a single-copy sequence from the human Y chromosome

R. Burk, K. Smith, P. Ma, 1985 .

Use of repetitive DNA for diagnosis of chromosomal rearrangements

R. Burk, K. E. Young, K. Smith, 1983, Human Genetics.

Partial purification and characterization of DNA from the human X chromosome.

F. Ruddle, B. Schmeckpeper, K. Smith, 1979, Proceedings of the National Academy of Sciences of the United States of America.

Prenatal diagnosis of sickle cell anemia by restriction and endonuclease analysis: HindIII polymorphisms in gamma-globin genes extend test applicability.

A. F. Scott, H. Kazazian, C. Boehm, 1980, Proceedings of the National Academy of Sciences of the United States of America.

Genetic control of macromolecular synthesis during development of an ascidian: Ascidia nigra.

K. Smith, Kirby D. Smith, 1967, The Journal of experimental zoology.

Isolation and characterization of a major tandem repeat family from the human X chromosome.

H. Willard, J. Sutherland, K. Smith, 1983, Nucleic acids research.

Characterization and evolution of a single-copy sequence from the human Y chromosome

R. Burk, K. Smith, P. Ma, 1985, Molecular and cellular biology.

Population heterogeneity of the Hpa I restriction site associated with the beta globin gene: implications for prenatal diagnosis.

A. F. Scott, H. Kazazian, C. Boehm, 1981, American journal of human genetics.

Evidence for increased prevalence of SRY mutations in XY females with complete rather than partial gonadal dysgenesis.

P. Goodfellow, C. Migeon, G. Berkovitz, 1992, American journal of human genetics.

Adjuvants to immunological methods for mRNA purification. Application to the isolation of mRNA for carbonic anhydrase I from rabbit reticulocytes.

K. E. Young, S. Boyer, K. Smith, 1983, The Journal of biological chemistry.

Repeated DNA of the human Y chromosome.

K. E. Young, B. Schmeckpeper, K. Smith, 1987, Development.

Abstracts of workshop presentations pp. 1106-1116

R. L. Miller, D. Cox, D. Ledbetter, 1989 .

SV40 recombinants carrying rabbit beta-globin gene coding sequences.

P. Leder, D. Hamer, S. Boyer, 1979, Cell.

Report of the committee on the genetic constitution of the Y chromosome.

J. Weissenbach, P. Goodfellow, K. Smith, 1988, Cytogenetics and cell genetics.

Treatment of sickle cell anemia with 5-azacytidine results in increased fetal hemoglobin production and is associated with nonrandom hypomethylation of DNA around the gamma-delta-beta-globin gene complex.

G. Dover, S. Boyer, S. Charache, 1983, Proceedings of the National Academy of Sciences of the United States of America.

Report of a kindred with X-linked (or autosomal dominant sex-limited) 46,XY partial gonadal dysgenesis.

P. Goodfellow, T. Ogata, C. Migeon, 1993, The Journal of clinical endocrinology and metabolism.

Nonrandom inactivation of the Y-bearing X chromosome in a 46,XX individual: evidence for the etiology of 46,XX true hermaphroditism.

P. Pearson, G. Stetten, C. Migeon, 1994, Cytogenetics and cell genetics.

The role of the sex-determining region Y gene in the etiology of 46,XX maleness.

P. Goodfellow, G. Stetten, C. Migeon, 1993, The Journal of clinical endocrinology and metabolism.

Report of the committee on the genetic constitution of the Y chromosome.

J. Weissenbach, P. Goodfellow, K. Smith, 1989, Cytogenetics and cell genetics.

Partial gonadal dysgenesis in a patient with a marker Y chromosome.

E. Jabs, C. Migeon, G. Berkovitz, 1992, American journal of medical genetics.

An anonymous single-copy X-chromosome RFLP for DXS72 from Xq13-Xq22 [HGM8 provisional no. DXS72].

H. Willard, J. Davis, B. Schmeckpeper, 1985, Nucleic acids research.

Production of F cells in sickle cell anemia: regulation by a genetic locus or loci separate from the beta-globin gene cluster.

S. Antonarakis, G. Dover, S. Boyer, 1984, Blood.

Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2.

D. Meyers, G. Dover, G. Serjeant, 1992, Blood.

An analysis of fetal hemoglobin variation in sickle cell disease: the relative contributions of the X-linked factor, beta-globin haplotypes, alpha-globin gene number, gender, and age.

G. Dover, R. Moore, G. Serjeant, 1995, Blood.

5-Azacytidine increases fetal hemoglobin production in a patient with sickle cell disease.

G. Dover, S. Boyer, S. Charache, 1983, Progress in clinical and biological research.

Adrenoleukodystrophy: Phenotypic variability and implications for therapy

H. Moser, A. Moser, J. Ott, 1992, Journal of Inherited Metabolic Disease.

A molecular basis for hemoglobin-H disease in American blacks.

A. F. Scott, H. Kazazian, K. E. Young, 1979, Blood.

The t(4;14) translocation in myeloma dysregulates both FGFR3 and a novel gene, MMSET, resulting in IgH/MMSET hybrid transcripts.

P. L. Bergsagel, W. Kuehl, Kerrington D. Smith, 1998, Blood.

The proportion of all point mutations which are unacceptable: an estimate based on hemoglobin amino acid and nucleotide sequences.

L. Kunkel, A. F. Scott, S. Boyer, 1978, Canadian journal of genetics and cytology. Journal canadien de genetique et de cytologie.

An Asian–Native American paternal lineage identified by RPS4Y resequencing and by microsatellite haplotyping

A. Bergen, K. Smith, D. Goldman, 1999, Annals of human genetics.

Transcripts homologous to a long repeated DNA element in the human genome.

A. F. Scott, B. Schmeckpeper, K. Smith, 1984, The Journal of biological chemistry.

Dinucleotide repeat polymorphisms at the DXS85, DXS16 and DXS43 loci.

K. Smith, G. Dover, Y. Chang, 1994, Human molecular genetics.

Prenatal diagnosis of hemoglobinopathies by restriction endonuclease analysis: pregnancies at risk for sickle cell anemia and S--O Arab disease.

A. F. Scott, H. Kazazian, G. Stetten, 1979, The Johns Hopkins medical journal.

Human Y-chromosome-specific reiterated DNA.

L. Kunkel, S. Boyer, K. Smith, 1976, Science.

Molecular aspects of chromatin elimination in Ascaris lumbricoides.

H. Ursprung, K. Smith, H. Tobler, 1972, Developmental biology.

Unequal crossing-over: a common basis of single alpha-globin genes in Asians and American blacks with hemoglobin-H disease.

A. F. Scott, H. Kazazian, T. Vik, 1980, Blood.

The molecular basis of hemoglobin Grady.

A. F. Scott, J. Clegg, H. Kazazian, 1981, American journal of human genetics.

The estimation of selection coefficients in Afrikaners: Huntington disease, porphyria variegata, and lipoid proteinosis.

K. Smith, O. Stine, 1990, American journal of human genetics.

Organization and heterogeneity of sequences within a repeating unit of human Y chromosome deoxyribonucleic acid.

L. Kunkel, S. Boyer, K. Smith, 1979, Biochemistry.

Abstracts of workshop presentations pp. 1075-1091

R. L. Miller, D. Cox, D. Ledbetter, 1989 .

Abstracts of workshop presentations pp. 1057-1074

R. L. Miller, D. Cox, D. Ledbetter, 1989 .

Abstracts of workshop presentations pp. 1023-1039

R. L. Miller, D. Cox, D. Ledbetter, 1989 .