A. C. Warren

发表

A genetic linkage map of 17 markers on human chromosome 21.

A. Chakravarti, S. Antonarakis, S. Slaugenhaupt, 1989, Genomics.

D21S210: A highly polymorphic (GT)n marker closely linked to the β-amyloid protein precursor (APP) gene

M. McInnis, A. Chakravarti, S. Antonarakis, 1993, Human Genetics.

Comparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndrome.

M. B. Peterson, A. Chakravarti, S. Antonarakis, 1992, American journal of human genetics.

Linkage Map on Chromosome 21q and the Association of a DNA Haplotype with a Propensity to Nondisjunction and Trisomy 21 a

A. Chakravarti, S. Antonarakis, J. Gusella, 1985, Annals of the New York Academy of Sciences.

A contiguous physical map of the pericentromeric region of chromosome 21q between D21Z1 and D21S13E.

M. McInnis, S. Antonarakis, L. Stuyver, 1993, Genomics.

Alphoid DNA polymorphisms for chromosome 21 can be distinguished from those of chromosome 13 using probes homologous to both.

S. Antonarakis, E. Jabs, D. Meyers, 1991, Genomics.

Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome.

A. Chakravarti, S. Antonarakis, S. Slaugenhaupt, 1987, Science.

The polydeoxyadenylate tract of Alu repetitive elements is polymorphic in the human genome.

S. Antonarakis, A. Bergen, A. C. Warren, 1990, Proceedings of the National Academy of Sciences of the United States of America.

A genetic linkage map of 27 markers on human chromosome 21.

A. Chakravarti, S. Antonarakis, S. Slaugenhaupt, 1991, Genomics.

Linkage mapping of the highly informative DNA marker D21S156 to human chromosome 21 using a polymorphic GT dinucleotide repeat.

J. Weber, A. Chakravarti, S. Antonarakis, 1990, Genomics.

Assignment of the Nance-Horan syndrome to the distal short arm of the X chromosome

S. Antonarakis, P. C. Huang, I. Maumenee, 1990, Human Genetics.

An alpha satellite DNA polymorphism specific for the centromeric region of chromosome 13.

A. Bowcock, S. Antonarakis, L. Farrer, 1990, Genomics.

Identification of flanking markers for the familial amyotrophic lateral sclerosis gene ALS1 on chromosome 21

J. Haines, M. McInnis, G. Rouleau, 1994, Journal of the Neurological Sciences.

Dinucleotide repeat (GT)n markers on chromosome 21.

M. McInnis, A. Chakravarti, S. Antonarakis, 1992, Genomics.

D21S215 is a (GT)n polymorphic marker close to centromeric alphoid sequences on chromosome 21.

M. McInnis, A. Chakravarti, S. Antonarakis, 1992, Genomics.

Two PstI DNA polymorphisms adjacent to the human gene for the interferon-induced p78 protein (MX1 gene).

S. Antonarakis, M. Petersen, A. C. Warren, 1989, Nucleic acids research.

β-Amyloid gene is not present in three copies in autopsy-validated Alzheimer's disease

D. Price, M. Folstein, S. Antonarakis, 1987 .

A linkage map of human chromosome 21:43 PCR markers at average intervals of 2.5 cM.

M G McInnis, T C Matise, A Chakravarti, 1993, Genomics.

Contributors and Participants

D. Cox, A. Kong, N. Mendell, 1982 .

The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms.

M. McInnis, A. Chakravarti, S. Antonarakis, 1992, American journal of human genetics.

A novel zinc finger cDNA with a polymorphic pentanucleotide repeat (ATTTT)n maps on human chromosome 19p.

S. Antonarakis, D. Avramopoulos, A. C. Warren, 1993, Genomics.

Reduced recombination rate on chromosomes 21 that have undergone nondisjunction.

A. Chakravarti, S. Antonarakis, S. Slaugenhaupt, 1986, Cold Spring Harbor symposia on quantitative biology.

Gene-centromere mapping and the study of non-disjunction in autosomal trisomies and ovarian teratomas.

U. Surti, A. Chakravarti, S. Antonarakis, 1989, Progress in clinical and biological research.