Ordering three DNA polymorphisms on human chromosome 3 by sperm typing.

[1]  N. Arnheim,et al.  Analysis of DNA sequence variation in single cells , 1991 .

[2]  N. Arnheim,et al.  PCR analysis of DNA sequences in single cells: single sperm gene mapping and genetic disease diagnosis. , 1990, Genomics.

[3]  L. Dubeau,et al.  Loss of heterozygosity on chromosomal segments 3p, 6q and 11p in human ovarian carcinomas. , 1990, Oncogene.

[4]  K. Lange,et al.  Multilocus ordering strategies based on sperm typing , 1990, Annals of Human Genetics.

[5]  A. Markham,et al.  AMPLIFICATION REFRACTORY MUTATION SYSTEM FOR PRENATAL DIAGNOSIS AND CARRIER ASSESSMENT IN CYSTIC FIBROSIS , 1989, The Lancet.

[6]  P. Devilee,et al.  At least four different chromosomal regions are involved in loss of heterozygosity in human breast carcinoma. , 1989, Genomics.

[7]  L. Hood,et al.  A common language for physical mapping of the human genome. , 1989, Science.

[8]  J. Yokota,et al.  Loss of heterozygosity on the short arm of chromosome 3 in carcinoma of the uterine cervix. , 1989, Cancer research.

[9]  Y. Nakamura,et al.  Loss of 3p or 11p alleles is associated with testicular cancer tumors. , 1989, Genomics.

[10]  P. Green,et al.  Regional and physical mapping studies characterizing the Greig polysyndactyly 3;7 chromosome translocation, t(3;7)(p21.1;p13). , 1989, Genomics.

[11]  U. Bergerheim,et al.  Deletion mapping in human renal cell carcinoma. , 1989, Cancer research.

[12]  J. Weber,et al.  Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction. , 1989, American journal of human genetics.

[13]  M. Litt,et al.  A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene. , 1989, American journal of human genetics.

[14]  H A Erlich,et al.  Generation of single-stranded DNA by the polymerase chain reaction and its application to direct sequencing of the HLA-DQA locus. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[15]  Henry A. Erlich,et al.  Amplification and analysis of DNA sequences in single human sperm and diploid cells , 1988, Nature.

[16]  G. Klein,et al.  Consistent chromosome 3p deletion and loss of heterozygosity in renal cell carcinoma. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[17]  H. Brauch,et al.  Loss of alleles of loci on the short arm of chromosome 3 in renal cell carcinoma , 1988, Nature.

[18]  K. Mullis,et al.  Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. , 1988, Science.

[19]  J. Osinga,et al.  Deletion of a DNA sequence at the chromosomal region 3p21 in all major types of lung cancer , 1987, Nature.

[20]  J. Minna,et al.  Molecular analysis of the short arm of chromosome 3 in small-cell and non-small-cell carcinoma of the lung. , 1987, The New England journal of medicine.

[21]  M. Daly,et al.  A genetic linkage map of the human genome , 1987, Cell.

[22]  S. Szücs,et al.  Specific chromosome aberration in human renal cell carcinoma , 1987, International journal of cancer.

[23]  P. Carroll,et al.  Abnormalities at chromosome region 3p12-14 characterize clear cell renal carcinoma. , 1987, Cancer genetics and cytogenetics.

[24]  E. Dietzsch,et al.  A three-allele RFLP recognised by an anonymous sequence localized to 3p14-p21 [D3S11 (E41)]. , 1986, Nucleic Acids Research.

[25]  K. Mullis,et al.  Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia. , 1985, Science.

[26]  T. Shows,et al.  DNA polymorphic loci mapped to human chromosomes 3, 5, 9, 11, 17, 18, and 22. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[27]  D. Barker,et al.  Restriction sites containing CpG show a higher frequency of polymorphism in human DNA , 1984, Cell.

[28]  J. Minna,et al.  Specific chromosome defect associated with human small-cell lung cancer; deletion 3p(14-23). , 1982, Science.

[29]  A. Rademaker,et al.  The frequency of aneuploidy among individual chromosomes in 6,821 human sperm chromosome complements. , 1990, Cytogenetics and cell genetics.

[30]  F. Collins,et al.  Fine-structure genetic mapping of human chromosomes using the polymerase chain reaction on single sperm: experimental design considerations. , 1989, American journal of human genetics.

[31]  K. Lange,et al.  Programs for pedigree analysis: Mendel, Fisher, and dGene , 1988, Genetic epidemiology.

[32]  J. DiPaolo,et al.  Nonrandom chromosome alterations in human malignant mesothelioma. , 1988, Cancer research.

[33]  J. Minna,et al.  Loss of heterozygosity of chromosome 3p markers in small-cell lung cancer , 1987, Nature.

[34]  K. Mullis,et al.  Specific synthesis of DNA in vitro via a polymerase-catalyzed chain reaction. , 1987, Methods in enzymology.

[35]  J. Whang‐Peng,et al.  Cytogenetic studies in ovarian cancer. , 1984, Cancer genetics and cytogenetics.