Antonarakis SE - Search Results

1

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

Peterson MB, Frantzen M, Antonarakis SE, Warren AC, Van Broeckhoven C, Chakravarti A, Cox TK, Lund C, Olsen B, Poulsen H, et al. Peterson MB, et al. Among authors: antonarakis se. Am J Hum Genet. 1992 Sep;51(3):516-25. Am J Hum Genet. 1992. PMID: 1386710 Free PMC article.

2

D21S210: a highly polymorphic (GT)n marker closely linked to the beta-amyloid protein precursor (APP) gene.

Warren AC, McInnis MG, Kalaitsidaki M, Cox TK, Blaschak J, Chakravarti A, Antonarakis SE. Warren AC, et al. Among authors: antonarakis se. Hum Genet. 1993 Mar;91(1):87-8. doi: 10.1007/BF00230232. Hum Genet. 1993. PMID: 8454294

3

Dinucleotide repeat (GT)n markers on chromosome 21.

Warren AC, McInnis MG, Blaschak J, Kaliatsidaki M, Petersen MB, Chakravarti A, Antonarakis SE. Warren AC, et al. Among authors: antonarakis se. Genomics. 1992 Nov;14(3):818-9. doi: 10.1016/s0888-7543(05)80198-3. Genomics. 1992. PMID: 1427915 Free article.

4

Cloning and linkage mapping of three polymorphic tetranucleotide (TAAA)n repeats on human chromosome 21.

Kalaitsidaki M, Cox T, Chakravarti A, Antonarakis SE. Kalaitsidaki M, et al. Among authors: antonarakis se. Genomics. 1992 Dec;14(4):1071-5. doi: 10.1016/s0888-7543(05)80131-4. Genomics. 1992. PMID: 1478649

5

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

Warren AC, Petersen MB, Van Hul W, McInnis MG, Van Broeckhoven C, Cox TK, Chakravarti A, Antonarakis SE. Warren AC, et al. Among authors: antonarakis se. Genomics. 1992 Aug;13(4):1365-7. doi: 10.1016/0888-7543(92)90072-z. Genomics. 1992. PMID: 1505976

6

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

Petersen MB, Slaugenhaupt SA, Lewis JG, Warren AC, Chakravarti A, Antonarakis SE. Petersen MB, et al. Among authors: antonarakis se. Genomics. 1991 Mar;9(3):407-19. doi: 10.1016/0888-7543(91)90406-5. Genomics. 1991. PMID: 1674496 Free article.

7

Chromosome 21 genetic linkage data set based on CEPH pedigrees.

Warren AC, Antonarakis SE, Chakravarti A. Warren AC, et al. Among authors: antonarakis se. Cytogenet Cell Genet. 1992;59(2-3):86-7. doi: 10.1159/000133207. Cytogenet Cell Genet. 1992. PMID: 1737517 No abstract available.

8

Linkage mapping of D21S171 to the distal long arm of human chromosome 21 using a polymorphic (AC)n dinucleotide repeat.

Petersen MB, Weber JL, Slaugenhaupt SA, Kwitek AE, McInnis MG, Chakravarti A, Antonarakis SE. Petersen MB, et al. Among authors: antonarakis se. Hum Genet. 1991 Aug;87(4):401-4. doi: 10.1007/BF00197156. Hum Genet. 1991. PMID: 1879826

9

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

Lewis JG, Weber JL, Petersen MB, Slaugenhaupt SA, Kwitek A, May PE, Warren AC, Chakravarti A, Antonarakis SE. Lewis JG, et al. Among authors: antonarakis se. Genomics. 1990 Oct;8(2):400-2. doi: 10.1016/0888-7543(90)90300-j. Genomics. 1990. PMID: 1979059

10

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

Zhu D, Alcorn DM, Antonarakis SE, Levin LS, Huang PC, Mitchell TN, Warren AC, Maumenee IH. Zhu D, et al. Among authors: antonarakis se. Hum Genet. 1990 Nov;86(1):54-8. doi: 10.1007/BF00205172. Hum Genet. 1990. PMID: 1979306

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