S. Wood

发表

A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates.

G. Lathrop, K. Buetow, Y. Nakamura, 1991, American journal of human genetics.

Linkage relationships and gene order around the locus for X-linked retinoschisis.

A. de la Chapelle, A. Eriksson, T. Kruse, 1988, American journal of human genetics.

Isolation of DNA fragments from a human chromosomal subregion by Alu PCR differential hybridization.

A. Brooks-Wilson, S. Wood, L. Bernard, 1991, Genomics.

Mapping of the pulmonary surfactant SP5 (SFTP2) locus to 8p21 and characterization of a microsatellite repeat marker that shows frequent loss of heterozygosity in human carcinomas.

J. Minna, C. Westbrook, P. Kelemen, 1994, Genomics.

Human chromosome 5 sequence primer amplifies Alu polymorphisms on chromosomes 2 and 17.

S. Wood, L. Bernard, 1993, Genome.

A 2.8 megabase YAC contig spanning D8S339, which is tightly linked to the Werner syndrome locus.

R. Bruskiewich, M. Schertzer, S. Wood, 1997, Genome.

Report of the Third International Workshop on Human Chromosome 8 Mapping. San Antonio, Texas, October 25-27, 1996.

P. O'Connell, S. Naylor, S. Daiger, 1996, Cytogenetics and cell genetics.

Report of the Third International Workshop on Human Chromosome 8 Mapping 1996

P. O'Connell, S. Naylor, S. Daiger, 1993 .

Familial 5q11.2----q13.3 segmental duplication cosegregating with multiple anomalies, including schizophrenia.

A. Bassett, S. Langlois, B. McGillivray, 1990, American journal of medical genetics.

A polymorphic complex dinucleotide repeat at the telomeric D8S7 locus.

M. Schertzer, S. Wood, Stephen Wood, 1992, Human heredity.

Juvenile sandhoff disease: Complementation tests with Sandhoff and Tay-Sachs disease using polyethylene glycol-induced cell fusion

S. Wood, 1978, Human Genetics.

Genemapping andmedical genetics

S. Wood, 1988 .

Human chromosome 8.

S. Wood, 1988, Journal of medical genetics.

Characterization of an inversion duplication of the short arm of chromosome 8 by fluorescent in situ hybridization.

F. Dill, K. G. Henderson, S. Wood, 1992, American journal of medical genetics.

Inverted tandem duplication generates a duplication deficiency of chromosome 8p

J. Sandercock, M. Schertzer, F. Dill, 1987, Clinical genetics.

Characterization of a human chromosome 8 cosmid library constructed from flow-sorted chromosomes.

J. Longmire, L. Deaven, H. Drabkin, 1992, Cytogenetics and cell genetics.

Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families.

K. Davies, A. Read, R. Thakker, 1990, Genomics.

A grandpaternally derived de novo deletion within Xp21 initially presenting in carrier females diagnosed as Kugelberg-Welander syndrome.

R. Shukin, P. Ray, R. Worton, 1988, American journal of medical genetics.

Report and abstracts of the First International Workshop on Human Chromosome 8 Mapping. Vancouver, British Columbia, May 2-4, 1993.

S. Daiger, S. Blanton, U. Bergerheim, 1993, Cytogenetics and cell genetics.

DNA typing in hereditary disease.

S. Langlois, S. Wood, 1991, Journal of chromatography.

A restriction-fragment-length difference detected by the anonymous probe DXS199 exhibits non-Mendelian inheritance.

S. Wood, T. Starr, 1988, American journal of human genetics.

Isolation and characterization of DNA probes from a flow-sorted human chromosome 8 library that detect restriction fragment length polymorphism (RFLP).

R. Shukin, S. Wood, T. Starr, 1986, American journal of human genetics.

Confirmation of linkage in X‐linked infantile spasms (West syndrome) and refinement of the disease locus to Xp21.3‐Xp22.1

S. Langlois, H. Bruyèrè, M. Lewis, 1999, Clinical genetics.

D8S7 is consistently deleted in inverted duplications of the short arm of chromosome 8 (inv dup 8p)

R. Tenconi, G. Floridia, M. Clementi, 1993, Human Genetics.

Genomic organization, expression, and chromosome location of the human SNAIL gene (SNAI1) and a related processed pseudogene (SNAI1P).

E. Jabs, K. Okajima, M. Schertzer, 1999, Genomics.

Human chromosome 8 linkage map based on short tandem repeat polymorphisms: effect of genotyping errors.

S. Daiger, S. Blanton, L. Sadler, 1992, Genomics.

Interstitial 7q deletion [46,XX,del(7)(pter----q21.1::q22----qter)] and the location of genes for beta-glucuronidase and cystic fibrosis.

D. Chitayat, S. Langlois, D. Kalousek, 1988, American journal of medical genetics.

Localization of a gene for a glutamate binding subunit of a NMDA receptor (GRINA) to 8q24.

R. Leach, E. Michaelis, B. Dupont, 1996, Genomics.

Genemapping andmedical genetics

S. Wood, 1988 .

Integrated mapping analysis of the Werner syndrome region of chromosome 8.

J. Weber, C. Disteche, M. Boehnke, 1994, Genomics.

Germinal mosaicism in Duchenne muscular dystrophy

B. McGillivray, S. Wood, 1988, Human Genetics.

Linkage Relationships andGeneOrderaroundtheLocus forX-linked Retinoschisis

S. Wood, 1988 .

Structural organization and genetic localization of the human bone morphogenetic protein 1/mammalian tolloid gene.

D. Greenspan, K. Takahara, S. Lee, 1995, Genomics.

Increasing evidence for a new X-linked mental retardation/epilepsy gene localized to Xp21.3-Xp22.1.

S. Langlois, H. Bruyèrè, M. E. Lewis, 1999, American journal of medical genetics.

Human SLUG gene organization, expression, and chromosome map location on 8q.

E. Jabs, M. Cohen, M. Schertzer, 1998, Genomics.

Identification of the human neuronal nicotinic cholinergic α2 receptor locus, (CHRNA2), within an 8p21 mapped locus, by sequence homology with rat DNA

M. Yaremko, M. Schertzer, S. Wood, 1995, Somatic cell and molecular genetics.

Support for founder effect for two lipoprotein lipase (LPL) gene mutations in French Canadians by analysis of GT microsatellites flanking the LPL gene

M. Hayden, Yuanhong Ma, M. Schertzer, 1993, Human Genetics.

A Detailed Multipoint MapofHumanChromosome4Provides Evidence forLinkage Heterogeneity andPosition-specifi c Recombination Rates

R. Shiang, Ping Yang, S. Wood, 1991 .

Sequence identity locates CEBPD and FGFR1 to mapped human loci within proximal 8p.

M. Yaremko, M. Schertzer, S. Wood, 1995, Cytogenetics and cell genetics.