The 1993–94 Généthon human genetic linkage map

[1]  Aravinda Chakravarti,et al.  Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map , 1994, Nature Genetics.

[2]  J. Weber,et al.  Integrated human genome–wide maps constructed using the CEPH reference panel , 1994, Nature Genetics.

[3]  G. Bernardi,et al.  The isochore organization of the human genome and its evolutionary history--a review. , 1993, Gene.

[4]  J. Weissenbach,et al.  A first-generation physical map of the human genome , 1993, Nature.

[5]  D. Cox,et al.  The development of sequence-tagged sites for human chromosome 4. , 1993, Human molecular genetics.

[6]  J. Weber,et al.  Mutation of human short tandem repeats. , 1993, Human molecular genetics.

[7]  Dinucleotide repeat polymorphism at the D14S99E locus. , 1993, Human molecular genetics.

[8]  R. Veenstra,et al.  Molecular cloning and functional expression of human connexin37, an endothelial cell gap junction protein. , 1993, The Journal of clinical investigation.

[9]  A. Bowcock,et al.  Microsatellite polymorphism linkage map of human chromosome 13q. , 1993, Genomics.

[10]  T. Barber,et al.  A highly informative dinucleotide repeat polymorphism at the D2S211 locus linked to ALPP, FN1 and TNP1. , 1993, Human molecular genetics.

[11]  R. Richards,et al.  Four dinucleotide repeat polymorphisms on human chromosome 16 at D16S289, D16S318, D16S319 and D16S320. , 1992, Human molecular genetics.

[12]  G. Gyapay,et al.  A second-generation linkage map of the human genome , 1992, Nature.

[13]  Z. Guo,et al.  Dinucleotide repeat polymorphism at the D18S37 locus. , 1992, Human molecular genetics.

[14]  T. Hudson,et al.  Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms. , 1992, Genomics.

[15]  G. Lathrop,et al.  Rat gene mapping using PCR-analyzed microsatellites. , 1992, Genetics.

[16]  G. Bernardi,et al.  The highest gene concentrations in the human genome are in telomeric bands of metaphase chromosomes. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[17]  E S Lander,et al.  A genetic map of the mouse suitable for typing intraspecific crosses. , 1992, Genetics.

[18]  B. Brophy,et al.  cDNA sequence of the pregnancy-specific β1-glycoprotein-11s (PSG-11s) , 1992 .

[19]  W. R. McCombie,et al.  Automated DNA sequencing and analysis of 106 kilobases from human chromosome 19q13.3 , 1992, Nature Genetics.

[20]  J. Weber,et al.  Linkage map of human chromosome 9 microsatellite polymorphisms. , 1992, Genomics.

[21]  K. Davies,et al.  ISOLATION AND CHARACTERIZATION OF HIGHLY POLYMORPHIC MARKERS AND RETINAL CDNAS IN THE VICINITIES OF X-LINKED INHERITED EYE DISEASE LOCI , 1991 .

[22]  A. Carrano,et al.  Molecular cloning of the human XRCC1 gene, which corrects defective DNA strand break repair and sister chromatid exchange , 1990, Molecular and cellular biology.

[23]  M. Mattei,et al.  Human uncoupling protein gene: Structure, comparison with rat gene, and assignment to the long arm of chromosome 4 , 1990, Journal of cellular biochemistry.

[24]  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.

[25]  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.

[26]  P. Bosma,et al.  Human plasminogen activator inhibitor-1 gene. Promoter and structural gene nucleotide sequences. , 1988, The Journal of biological chemistry.

[27]  J M Lalouel,et al.  A primary genetic map of markers of human chromosome 10. , 1988, Genomics.

[28]  E. Lander,et al.  Construction of multilocus genetic linkage maps in humans. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[29]  G. Lathrop,et al.  Easy calculations of lod scores and genetic risks on small computers. , 1984, American journal of human genetics.