-
1
-
-
0028064998
-
An autosomal locus causing autoimmune disease: Autoimmune polyglandular disease type I assigned to chromosome 21
-
Aaltonen J., Björses P., Sandkuijl L., Perheentupa J., Peltonen L. An autosomal locus causing autoimmune disease: Autoimmune polyglandular disease type I assigned to chromosome 21. Nat. Genet. 8:1994;83-87.
-
(1994)
Nat. Genet.
, vol.8
, pp. 83-87
-
-
Aaltonen, J.1
Björses, P.2
Sandkuijl, L.3
Perheentupa, J.4
Peltonen, L.5
-
2
-
-
0010557596
-
Chromosomal assignments of genes coding for T-200 (CD45) and LFA-1 beta (CD18) antigens to human chromosome 1 and 21 respectively
-
Akao Y., Utsumi K. R., Naito K., Ueda R., Takahashi T., Yamada K. Chromosomal assignments of genes coding for T-200 (CD45) and LFA-1 beta (CD18) antigens to human chromosome 1 and 21 respectively. Cytogenet. Cell Genet. 46:1987;568.
-
(1987)
Cytogenet. Cell Genet.
, vol.46
, pp. 568
-
-
Akao, Y.1
Utsumi, K.R.2
Naito, K.3
Ueda, R.4
Takahashi, T.5
Yamada, K.6
-
3
-
-
0023898362
-
Gene encoding the β subunit of S100 protein is on chromosome 21: Implications for Down syndrome
-
Allore R., O'Hanlon D., Price R., Neilson K., Willard H. F., Cox D. R., Marks A., Dunn R. J. Gene encoding the β subunit of S100 protein is on chromosome 21: Implications for Down syndrome. Science. 239:1988;1311-1313.
-
(1988)
Science
, vol.239
, pp. 1311-1313
-
-
Allore, R.1
O'Hanlon, D.2
Price, R.3
Neilson, K.4
Willard, H.F.5
Cox, D.R.6
Marks, A.7
Dunn, R.J.8
-
4
-
-
0025369509
-
A 3.5 genome equivalent multi access YAC library: Construction, characterization and storage
-
Anand R., Riley J. H., Butler R., Smith J. C., Markham A. F. A 3.5 genome equivalent multi access YAC library: Construction, characterization and storage. Nucleic Acids Res. 18:1990;1951-1956.
-
(1990)
Nucleic Acids Res.
, vol.18
, pp. 1951-1956
-
-
Anand, R.1
Riley, J.H.2
Butler, R.3
Smith, J.C.4
Markham, A.F.5
-
5
-
-
0024805395
-
The isochore organization of the human genome
-
Bernardi G. The isochore organization of the human genome. Annu. Rev. Genet. 23:1989;637-661.
-
(1989)
Annu. Rev. Genet.
, vol.23
, pp. 637-661
-
-
Bernardi, G.1
-
6
-
-
0029836686
-
Genetic homogeneity of autoimmune polyglandular disease type I
-
Björses P., Aaltonen J., Vikman A., Perheentupa J., Ben-Zion G., Chiumello G., Dahl N., Heideman P., Hoorweg-Njiman J. J. G., Mathivon L., Mullis P. E., Pohl M., Ritzen M., Romeo G., Shapiro M. S., Smith C. S., Solyom J., Zlotogora J., Peltonen L. Genetic homogeneity of autoimmune polyglandular disease type I. Am. J. Hum. Genet. 59:1996;879-886.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 879-886
-
-
Björses, P.1
Aaltonen, J.2
Vikman, A.3
Perheentupa, J.4
Ben-Zion, G.5
Chiumello, G.6
Dahl, N.7
Heideman, P.8
Hoorweg-Njiman, J.J.G.9
Mathivon, L.10
Mullis, P.E.11
Pohl, M.12
Ritzen, M.13
Romeo, G.14
Shapiro, M.S.15
Smith, C.S.16
Solyom, J.17
Zlotogora, J.18
Peltonen, L.19
-
7
-
-
0029013276
-
A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination
-
Blouin J.-L., Christie D. H., Gos A., Lynn A., Morris M. A., Ledbetter D., Chakravarti A., Antonarakis S. E. A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination. Am. J. Hum. Genet. 57:1995;388-394.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 388-394
-
-
Blouin, J.-L.1
Christie, D.H.2
Gos, A.3
Lynn, A.4
Morris, M.A.5
Ledbetter, D.6
Chakravarti, A.7
Antonarakis, S.E.8
-
8
-
-
0029883986
-
Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3
-
Bonné-Tamir B., DeStefano A. L., Briggs C. E., Adair R., Franklyn B., Weiss S., Korostishevsky M., Frydman M., Baldwin C. T., Farrer L. A. Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3. Am. J. Hum. Genet. 58:1996;1254-1259.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 1254-1259
-
-
Bonné-Tamir, B.1
DeStefano, A.L.2
Briggs, C.E.3
Adair, R.4
Franklyn, B.5
Weiss, S.6
Korostishevsky, M.7
Frydman, M.8
Baldwin, C.T.9
Farrer, L.A.10
-
9
-
-
0025617086
-
Potential gene sequence isolation and regional mapping in human chromosome 21
-
Brahe C., Tassone F., Millington-Ward A., Serra A., Gardiner K. Potential gene sequence isolation and regional mapping in human chromosome 21. Am. J. Med. Genet. (Suppl.). 7:1990;120-124.
-
(1990)
Am. J. Med. Genet. (Suppl.)
, vol.7
, pp. 120-124
-
-
Brahe, C.1
Tassone, F.2
Millington-Ward, A.3
Serra, A.4
Gardiner, K.5
-
10
-
-
0024561587
-
Molecular cloning of human telomeres in yeast
-
Brown W. R. A. Molecular cloning of human telomeres in yeast. Nature. 338:1989;774-776.
-
(1989)
Nature
, vol.338
, pp. 774-776
-
-
Brown, W.R.A.1
-
11
-
-
0030218072
-
Localization of a human homolog of the mouse pericentrin gene (PCNT) to chromosome 21qter
-
Chen H., Gos A., Morris M. A., Antonarakis S. E. Localization of a human homolog of the mouse pericentrin gene (PCNT) to chromosome 21qter. Genomics. 35:1996;620-624.
-
(1996)
Genomics
, vol.35
, pp. 620-624
-
-
Chen, H.1
Gos, A.2
Morris, M.A.3
Antonarakis, S.E.4
-
12
-
-
0028025053
-
Isolation and mapping of human chromosome 21 cDNA: Progress in constructing a chromosome 21 expression map
-
Cheng J. F., Boyartchuk V., Zhu Y. Isolation and mapping of human chromosome 21 cDNA: Progress in constructing a chromosome 21 expression map. Genomics. 23:1994;75-84.
-
(1994)
Genomics
, vol.23
, pp. 75-84
-
-
Cheng, J.F.1
Boyartchuk, V.2
Zhu, Y.3
-
13
-
-
0026738541
-
Continuum of overlapping clones spanning the entire human chromosome 21q
-
Chumakov I., Rigault P., Guillou S., Ougen P., Billaut A., Guasconi G., Gervy P., LeGall I., Soularue P., Grinas L., Bougueleret L., Bellanné-Chantelot C., Lacroix B., Barillot E., Gesnouin P., Pook S., Vaysseix G., Frelat G., Schmitz A., Sambucy J. L., Bosch A., Estivill X., Weissenbach J., Vignal A., Riethman H., Cox D., Patterson D., Gardiner K., Hattori M., Sakaki Y., Ichikawa H., Ohki M., Le Paslier D., Heilig R., Antonarakis S., Cohen D. Continuum of overlapping clones spanning the entire human chromosome 21q. Nature. 359:1992;380-387.
-
(1992)
Nature
, vol.359
, pp. 380-387
-
-
Chumakov, I.1
Rigault, P.2
Guillou, S.3
Ougen, P.4
Billaut, A.5
Guasconi, G.6
Gervy, P.7
LeGall, I.8
Soularue, P.9
Grinas, L.10
Bougueleret, L.11
Bellanné-Chantelot, C.12
Lacroix, B.13
Barillot, E.14
Gesnouin, P.15
Pook, S.16
Vaysseix, G.17
Frelat, G.18
Schmitz, A.19
Sambucy, J.L.20
Bosch, A.21
Estivill, X.22
Weissenbach, J.23
Vignal, A.24
Riethman, H.25
Cox, D.26
Patterson, D.27
Gardiner, K.28
Hattori, M.29
Sakaki, Y.30
Ichikawa, H.31
Ohki, M.32
Le Paslier, D.33
Heilig, R.34
Antonarakis, S.35
Cohen, D.36
more..
-
14
-
-
0028301317
-
The distribution of CpG islands in mammalian chromosomes
-
Craig J. M., Bickmore W. A. The distribution of CpG islands in mammalian chromosomes. Nat. Genet. 7:1994;376-381.
-
(1994)
Nat. Genet.
, vol.7
, pp. 376-381
-
-
Craig, J.M.1
Bickmore, W.A.2
-
15
-
-
0025880778
-
Accurate evaluation of the sizes of DNA fragments (from 30 to 4700 kb) in pulse field electrophoresis
-
Crété N., Delabar J., Sinet P.-M., Créau-Goldberg N. Accurate evaluation of the sizes of DNA fragments (from 30 to 4700 kb) in pulse field electrophoresis. BioTechniques. 11:1991;42-46.
-
(1991)
BioTechniques
, vol.11
, pp. 42-46
-
-
Crété, N.1
Delabar, J.2
Sinet, P.-M.3
Créau-Goldberg, N.4
-
16
-
-
0027310595
-
Partial physical map of human chromosome 21 from fibroblast and lymphocyte DNA
-
Crété N., Delabar J.-M., Rahmani Z., Yaspo M.-L., Kraus J., Marks A., Sinet P.-M., Créau-Goldberg N. Partial physical map of human chromosome 21 from fibroblast and lymphocyte DNA. Hum. Genet. 91:1993a;245-253.
-
(1993)
Hum. Genet.
, vol.91
, pp. 245-253
-
-
Crété, N.1
Delabar, J.-M.2
Rahmani, Z.3
Yaspo, M.-L.4
Kraus, J.5
Marks, A.6
Sinet, P.-M.7
Créau-Goldberg, N.8
-
17
-
-
0027793704
-
Mapping of the Down syndrome chromosome region: Establishment of a YAC contig spanning 1.2 megabases
-
Crété N., Gosset P., Theophile D., Duterque-Coquillaud M., Blouin J. L., Vayssette C., Sinet P.-M., Créau-Goldberg N. Mapping of the Down syndrome chromosome region: Establishment of a YAC contig spanning 1.2 megabases. Eur. J. Hum. Genet. 1:1993b;51-63.
-
(1993)
Eur. J. Hum. Genet.
, vol.1
, pp. 51-63
-
-
Crété, N.1
Gosset, P.2
Theophile, D.3
Duterque-Coquillaud, M.4
Blouin, J.L.5
Vayssette, C.6
Sinet, P.-M.7
Créau-Goldberg, N.8
-
18
-
-
0027874350
-
Molecular mapping of twenty-four features of Down syndrome on chromosome 21
-
Delabar J. M., Theophile D., Rahmani Z., Chettouh Z., Blouin J. L., Prieur M., Noel B., Sinet P. M. Molecular mapping of twenty-four features of Down syndrome on chromosome 21. Eur. J. Hum. Genet. 1:1993;114-124.
-
(1993)
Eur. J. Hum. Genet.
, vol.1
, pp. 114-124
-
-
Delabar, J.M.1
Theophile, D.2
Rahmani, Z.3
Chettouh, Z.4
Blouin, J.L.5
Prieur, M.6
Noel, B.7
Sinet, P.M.8
-
19
-
-
0029885038
-
Affected-sib-pair analyses reveal support of prior evidence for a susceptibility locus for bipolar disorder, on 21q
-
Detera-Wadleigh S. D., Badner J. A., Goldin L. R., Berrettini W. H., Sanders A. R., Rollins D. Y., Turner G., Moses T., Haerian H., Muniec D., Nurnberger J. I. Jr., Gershon E. S. Affected-sib-pair analyses reveal support of prior evidence for a susceptibility locus for bipolar disorder, on 21q. Am. J. Hum. Genet. 58:1996;1279-1285.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 1279-1285
-
-
Detera-Wadleigh, S.D.1
Badner, J.A.2
Goldin, L.R.3
Berrettini, W.H.4
Sanders, A.R.5
Rollins, D.Y.6
Turner, G.7
Moses, T.8
Haerian, H.9
Muniec, D.10
Nurnberger J.I., Jr.11
Gershon, E.S.12
-
20
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5,264 microsatellites
-
Dib C., Fauré S., Fizames C., Samson d., Drouot N., Vignal A., Millasseau P., Marc S., Hazan J., Seboun E., Lathrop M., Gyapay G., Morissette J., Weissenbach J. A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature. 380:1996;152-154.
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Fauré, S.2
Fizames, C.3
Samson, D.4
Drouot, N.5
Vignal, A.6
Millasseau, P.7
Marc, S.8
Hazan, J.9
Seboun, E.10
Lathrop, M.11
Gyapay, G.12
Morissette, J.13
Weissenbach, J.14
-
21
-
-
0028344760
-
3.6 Mb genomic and YAC physical map of the Down syndrome chromosome region on chromosome 21
-
Dufresne-Zacharia M. C., Dahmane N., Theophile D., Orti R., Chettouh Z., Sinet P. M., Delabar J. M. 3.6 Mb genomic and YAC physical map of the Down syndrome chromosome region on chromosome 21. Genomics. 19:1994;462-469.
-
(1994)
Genomics
, vol.19
, pp. 462-469
-
-
Dufresne-Zacharia, M.C.1
Dahmane, N.2
Theophile, D.3
Orti, R.4
Chettouh, Z.5
Sinet, P.M.6
Delabar, J.M.7
-
22
-
-
0030589716
-
Structural organization of multiple alphoid subsets coexisting on human chromosomes 1, 4, 5, 7, 9, 15, 18, and 19
-
Finelli P., Antonacci R., Marzella R., Lonoce A., Archidiacono N., Rocchi M. Structural organization of multiple alphoid subsets coexisting on human chromosomes 1, 4, 5, 7, 9, 15, 18, and 19. Genomics. 38:1996;325-330.
-
(1996)
Genomics
, vol.38
, pp. 325-330
-
-
Finelli, P.1
Antonacci, R.2
Marzella, R.3
Lonoce, A.4
Archidiacono, N.5
Rocchi, M.6
-
23
-
-
0025369193
-
A compositional map of human chromosome 21
-
Gardiner K., Aissani B., Bernardi G. A compositional map of human chromosome 21. EMBO J. 9:1990;1853-1858.
-
(1990)
EMBO J.
, vol.9
, pp. 1853-1858
-
-
Gardiner, K.1
Aissani, B.2
Bernardi, G.3
-
24
-
-
0028848581
-
Localization of cDNAs to a region poorly represented in the CEPH chromosome 21 YAC contig: Candidate genes for genetic diseases mapped to 21q22.3
-
Gardiner K., Ichikawa H., Ohki M., Patterson D., Cheng J. F. Localization of cDNAs to a region poorly represented in the CEPH chromosome 21 YAC contig: Candidate genes for genetic diseases mapped to 21q22.3. Genomics. 30:1995;376-379.
-
(1995)
Genomics
, vol.30
, pp. 376-379
-
-
Gardiner, K.1
Ichikawa, H.2
Ohki, M.3
Patterson, D.4
Cheng, J.F.5
-
25
-
-
0029240247
-
A high-resolution map of 1.6 Mb in the Down syndrome region: A new map between D21S55 and ETS2
-
Gosset P., Crété N., Ghezala G. A., Théophile D., Van Broeckhoven C., Vayssettes C., Sinet P. M., Créau N. A high-resolution map of 1.6 Mb in the Down syndrome region: A new map between D21S55 and ETS2. Mamm. Genome. 6:1995;127-130.
-
(1995)
Mamm. Genome
, vol.6
, pp. 127-130
-
-
Gosset, P.1
Crété, N.2
Ghezala, G.A.3
Théophile, D.4
Van Broeckhoven, C.5
Vayssettes, C.6
Sinet, P.M.7
Créau, N.8
-
26
-
-
0028803889
-
Head to tail organization of the human COL6A1 and COL6A2 genes by fiber-FISH
-
Heiskanen M., Saitta B., Palotie A., Chu M. L. Head to tail organization of the human COL6A1 and COL6A2 genes by fiber-FISH. Genomics. 29:1995;801-803.
-
(1995)
Genomics
, vol.29
, pp. 801-803
-
-
Heiskanen, M.1
Saitta, B.2
Palotie, A.3
Chu, M.L.4
-
27
-
-
17744416866
-
BAC and PAC contigs covering 3.5 Mb of the Down syndrome congenital heart disease region between D21S55 and MX1 on chromosome 21
-
Hubert R. S., Mitchell S., Chen X. N., Ekmekji K., Gadomski C., Sun Z., Noya D., Kim U. J., Chen C., Shizuya H., Simon M., de Jong P. J., Korenberg J. R. BAC and PAC contigs covering 3.5 Mb of the Down syndrome congenital heart disease region between D21S55 and MX1 on chromosome 21. Genomics. 41:1997;218-266.
-
(1997)
Genomics
, vol.41
, pp. 218-266
-
-
Hubert, R.S.1
Mitchell, S.2
Chen, X.N.3
Ekmekji, K.4
Gadomski, C.5
Sun, Z.6
Noya, D.7
Kim, U.J.8
Chen, C.9
Shizuya, H.10
Simon, M.11
De Jong, P.J.12
Korenberg, J.R.13
-
28
-
-
0027184311
-
-
Ichikawa H., Hosoda F., Arai Y., Shimizu K., Ohira M., Ohki M. ANot. Nat. Genet. 4:1993;361-366.
-
(1993)
ANot. Nat. Genet.
, vol.4
, pp. 361-366
-
-
Ichikawa, H.1
Hosoda, F.2
Arai, Y.3
Shimizu, K.4
Ohira, M.5
Ohki, M.6
-
29
-
-
0028318417
-
A new bacteriophage P1-derived vector for the progagation of large human DNA fragments
-
Ioannou P. A., Amemiya C. T., Garnes J., Kroisel P. M., Chizuya H., Chen C., Batzer M. A., de Jong P. J. A new bacteriophage P1-derived vector for the progagation of large human DNA fragments. Nat. Genet. 6:1994;84-89.
-
(1994)
Nat. Genet.
, vol.6
, pp. 84-89
-
-
Ioannou, P.A.1
Amemiya, C.T.2
Garnes, J.3
Kroisel, P.M.4
Chizuya, H.5
Chen, C.6
Batzer, M.A.7
De Jong, P.J.8
-
30
-
-
0029771617
-
Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contractures
-
Jöbsis G. J., Keizers H., Vreijling J. P., de Visser M., Speer M. C., Wolterman R. A., Baas F., Bolhuis P. A. Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contractures. Nat. Genet. 14:1996;113-115.
-
(1996)
Nat. Genet.
, vol.14
, pp. 113-115
-
-
Jöbsis, G.J.1
Keizers, H.2
Vreijling, J.P.3
De Visser, M.4
Speer, M.C.5
Wolterman, R.A.6
Baas, F.7
Bolhuis, P.A.8
-
31
-
-
0025941471
-
Identification of deletion mutations and three new genes at the familial polyposis locus
-
Joslyn G., Carison M., Thilveria A., Albertsen H., Gelbert L., Samowitz W., Groden J., Stevens J., Spirio L., Robertson M., Sargeant L., Krapcho K., Wolff E., Burt R., Hughes J. P., Warrington J., McPherson J., Wasmuth J., LePaslier D., Abderrahim H., Cohen D., Leppert M., White R. Identification of deletion mutations and three new genes at the familial polyposis locus. Cell. 66:1991;601-613.
-
(1991)
Cell
, vol.66
, pp. 601-613
-
-
Joslyn, G.1
Carison, M.2
Thilveria, A.3
Albertsen, H.4
Gelbert, L.5
Samowitz, W.6
Groden, J.7
Stevens, J.8
Spirio, L.9
Robertson, M.10
Sargeant, L.11
Krapcho, K.12
Wolff, E.13
Burt, R.14
Hughes, J.P.15
Warrington, J.16
McPherson, J.17
Wasmuth, J.18
LePaslier, D.19
Abderrahim, H.20
Cohen, D.21
Leppert, M.22
White, R.23
more..
-
32
-
-
0031177791
-
Identification and mapping of a novel human gene, HRMT1L1, homologous to the rat protein arginineN
-
Katsanis N., Yaspo M. L., Fisher E. M. C. Identification and mapping of a novel human gene, HRMT1L1, homologous to the rat protein arginineN. Mamm. Genome. 8:1997;526-529.
-
(1997)
Mamm. Genome
, vol.8
, pp. 526-529
-
-
Katsanis, N.1
Yaspo, M.L.2
Fisher, E.M.C.3
-
33
-
-
0025170497
-
Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype
-
Korenberg J. R., Kawashima H., Pulst S. M., Ikeuchi T., Ogasawara N., Yamamoto K., Schonberg S. A., West R., Allen L., Magenis E., Ikawa K., Taniguchi N., Epstein C. J. Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype. Am. J. Hum. Genet. 47:1990;236-246.
-
(1990)
Am. J. Hum. Genet.
, vol.47
, pp. 236-246
-
-
Korenberg, J.R.1
Kawashima, H.2
Pulst, S.M.3
Ikeuchi, T.4
Ogasawara, N.5
Yamamoto, K.6
Schonberg, S.A.7
West, R.8
Allen, L.9
Magenis, E.10
Ikawa, K.11
Taniguchi, N.12
Epstein, C.J.13
-
34
-
-
0026583894
-
Down syndrome: Molecular mapping of the congenital heart disease and duodenal stenosis
-
Korenberg J. R., Bradley C., Disteche C. M. Down syndrome: Molecular mapping of the congenital heart disease and duodenal stenosis. Am. J. Hum. Genet. 50:1992;294-302.
-
(1992)
Am. J. Hum. Genet.
, vol.50
, pp. 294-302
-
-
Korenberg, J.R.1
Bradley, C.2
Disteche, C.M.3
-
35
-
-
0028341315
-
Down syndrome phenotypes: The consequences of chromosomal imbalance
-
Korenberg J. R., Chen X. N., Schipper R., Sun Z., Gonsky R., Gerwehr S., Carpenter N., Daumer C., Dignan P., Disteche C., Graham J. M. Jr., Hugdins L., McGillivray B., Myiazaki K., Ogasawara N., Park J. M., Pagon R., Pueschel S., Sack G., Say B., Schuffenahuer S., Soukup S., Yamanaka T. Down syndrome phenotypes: The consequences of chromosomal imbalance. Proc. Natl. Acad. Sci. USA. 91:1994;4997-5001.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 4997-5001
-
-
Korenberg, J.R.1
Chen, X.N.2
Schipper, R.3
Sun, Z.4
Gonsky, R.5
Gerwehr, S.6
Carpenter, N.7
Daumer, C.8
Dignan, P.9
Disteche, C.10
Graham J.M., Jr.11
Hugdins, L.12
McGillivray, B.13
Myiazaki, K.14
Ogasawara, N.15
Park, J.M.16
Pagon, R.17
Pueschel, S.18
Sack, G.19
Say, B.20
Schuffenahuer, S.21
Soukup, S.22
Yamanaka, T.23
more..
-
37
-
-
0002018172
-
A high resolution physical map of the distal part of chromosome 21
-
Lapenta V., Vitali T., Blouin J.-L., Créau N., Lalioti M., Antonarakis S. E., Brahe C. A high resolution physical map of the distal part of chromosome 21. Eur. J. Hum. Genet. 4:1996;62.
-
(1996)
Eur. J. Hum. Genet.
, vol.4
, pp. 62
-
-
Lapenta, V.1
Vitali, T.2
Blouin, J.-L.3
Créau, N.4
Lalioti, M.5
Antonarakis, S.E.6
Brahe, C.7
-
38
-
-
0031104910
-
SMT3A, a human homologue of theS. cerevisiae
-
Lapenta V., Chiurazzi P., van der Spek P., Pizzuti A., Hanaoka F., Brahe C. SMT3A, a human homologue of theS. cerevisiae. Genomics. 40:1997;362-366.
-
(1997)
Genomics
, vol.40
, pp. 362-366
-
-
Lapenta, V.1
Chiurazzi, P.2
Van Der Spek, P.3
Pizzuti, A.4
Hanaoka, F.5
Brahe, C.6
-
39
-
-
0025897085
-
Yeast artificial chromosome libraries containing large inserts from mouse and human DNA
-
Larin Z., Monaco A. P., Lehrach H. Yeast artificial chromosome libraries containing large inserts from mouse and human DNA. Proc. Natl. Acad. Sci. USA. 88:1991;4123-4127.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 4123-4127
-
-
Larin, Z.1
Monaco, A.P.2
Lehrach, H.3
-
41
-
-
0024712933
-
Molecular genetic approach to the characterization of the "Down syndrome region" of chromosome 21
-
McCormick M. K., Schinzel A., Petersen M. B., Stetten G., Driscoll D. J., Cantu E. S., Tranebjaerg L., Mikkelsen M., Watkins P. C., Antonarakis S. E. Molecular genetic approach to the characterization of the "Down syndrome region" of chromosome 21. Genomics. 5:1989;325-331.
-
(1989)
Genomics
, vol.5
, pp. 325-331
-
-
McCormick, M.K.1
Schinzel, A.2
Petersen, M.B.3
Stetten, G.4
Driscoll, D.J.5
Cantu, E.S.6
Tranebjaerg, L.7
Mikkelsen, M.8
Watkins, P.C.9
Antonarakis, S.E.10
-
42
-
-
0031569889
-
Cloning of a human RNA editing deaminase (ADARB1) of glutamate receptors that maps to chromosome 21q22.3
-
Mittaz L., Scott H. S., Rossier C., Seeburg P. H., Higuchi M., Antonarakis S. E. Cloning of a human RNA editing deaminase (ADARB1) of glutamate receptors that maps to chromosome 21q22.3. Genomics. 41:1997;210-217.
-
(1997)
Genomics
, vol.41
, pp. 210-217
-
-
Mittaz, L.1
Scott, H.S.2
Rossier, C.3
Seeburg, P.H.4
Higuchi, M.5
Antonarakis, S.E.6
-
43
-
-
0028787577
-
Physical mapping of the holoprosencephaly critical region in 21q22.3, exclusion of SIM2 as a candidate gene for holoprosencephaly, and mapping of SIM2 to a region of chromosome 21 important for Down syndrome
-
Muenke M., Bone L. J., Mitchell H. F., Hart I., Walton K., Hall-Johnson K., Ippel E. F., Dietz-Band J., Kvaløy K., Fan C-M., Tessier-Lavigne M., Patterson D. Physical mapping of the holoprosencephaly critical region in 21q22.3, exclusion of SIM2 as a candidate gene for holoprosencephaly, and mapping of SIM2 to a region of chromosome 21 important for Down syndrome. Am. J. Hum. Genet. 57:1995;1074-1079.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 1074-1079
-
-
Muenke, M.1
Bone, L.J.2
Mitchell, H.F.3
Hart, I.4
Walton, K.5
Hall-Johnson, K.6
Ippel, E.F.7
Dietz-Band, J.8
Kvaløy, K.9
Fan, C.-M.10
Tessier-Lavigne, M.11
Patterson, D.12
-
44
-
-
0028210848
-
Cloning of cDNA and genomic DNA encoding human type XVII collagen and localization of the α1(XVIII) collagen gene to mouse chromosome 10 and human chromosome 21
-
Oh S. P., Warman M. L., Seldin M. F., Cheng S.-D., Knoll J. H. M., Timmons S., Olson B. R. Cloning of cDNA and genomic DNA encoding human type XVII collagen and localization of the α1(XVIII) collagen gene to mouse chromosome 10 and human chromosome 21. Genomics. 19:1994;494-499.
-
(1994)
Genomics
, vol.19
, pp. 494-499
-
-
Oh, S.P.1
Warman, M.L.2
Seldin, M.F.3
Cheng, S.-D.4
Knoll, J.H.M.5
Timmons, S.6
Olson, B.R.7
-
45
-
-
17644430449
-
A 1.6-Mb P1-based physical map of the Down syndrome region of the chromosome 21
-
Ohira M., Ichikawa H., Suzuki E., Iwaki M., Suzuki K., Saito-Ohara F., Ikeuchi T., Chumakov I., Tanahashi H., Tashiro K., Sakaki Y., Ohki M. A 1.6-Mb P1-based physical map of the Down syndrome region of the chromosome 21. Genomics. 33:1996;65-74.
-
(1996)
Genomics
, vol.33
, pp. 65-74
-
-
Ohira, M.1
Ichikawa, H.2
Suzuki, E.3
Iwaki, M.4
Suzuki, K.5
Saito-Ohara, F.6
Ikeuchi, T.7
Chumakov, I.8
Tanahashi, H.9
Tashiro, K.10
Sakaki, Y.11
Ohki, M.12
-
46
-
-
0029913925
-
An integrated map with cosmid/PAC contigs of a 4-Mb Down syndrome critical region
-
Osoegawa K., Susukida R., Okano S., Kudoh J., Minoshima S., Shimizu N., De Jong P. J., Groet J., Ives J., Lehrach H., Nizetic D., Soeda E. An integrated map with cosmid/PAC contigs of a 4-Mb Down syndrome critical region. Genomics. 32:1996;375-387.
-
(1996)
Genomics
, vol.32
, pp. 375-387
-
-
Osoegawa, K.1
Susukida, R.2
Okano, S.3
Kudoh, J.4
Minoshima, S.5
Shimizu, N.6
De Jong, P.J.7
Groet, J.8
Ives, J.9
Lehrach, H.10
Nizetic, D.11
Soeda, E.12
-
47
-
-
0028076769
-
A high resolution physical map of 2.5 Mbp of the Down syndrome region on chromosome 21
-
Patil N., Peterson A., Rothman A., de Jong P. J., Myers R. M., Cox D. R. A high resolution physical map of 2.5 Mbp of the Down syndrome region on chromosome 21. Hum. Mol. Genet. 3:1994;1811-1817.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1811-1817
-
-
Patil, N.1
Peterson, A.2
Rothman, A.3
De Jong, P.J.4
Myers, R.M.5
Cox, D.R.6
-
48
-
-
13344269666
-
Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1)
-
Pennacchio L. A., Lehesjoki A.-E., Stone N. E., Willour V. L., Virtaneva K., Miao J., D'Amato E., Ramirez L., Faham M., Koskiniemi M., Warrington J. A., Norio R., de la Chapelle A., Cox D. R., Myers R. M. Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1). Science. 271:1996;1731-1733.
-
(1996)
Science
, vol.271
, pp. 1731-1733
-
-
Pennacchio, L.A.1
Lehesjoki, A.-E.2
Stone, N.E.3
Willour, V.L.4
Virtaneva, K.5
Miao, J.6
D'Amato, E.7
Ramirez, L.8
Faham, M.9
Koskiniemi, M.10
Warrington, J.A.11
Norio, R.12
De La Chapelle, A.13
Cox, D.R.14
Myers, R.M.15
-
49
-
-
0012083187
-
Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome
-
Rahmani Z., Blouin J. L., Créau-Goldberg N., Watkins P. C., Mattei J. F., Poissonnier M., Prieur M., Chettouh Z., Nicole A., Aurias A., Sinet P. M., Delabar J. M. Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome. Proc. Natl. Acad. Sci. USA. 86:1989;5958-5962.
-
(1989)
Proc. Natl. Acad. Sci. USA
, vol.86
, pp. 5958-5962
-
-
Rahmani, Z.1
Blouin, J.L.2
Créau-Goldberg, N.3
Watkins, P.C.4
Mattei, J.F.5
Poissonnier, M.6
Prieur, M.7
Chettouh, Z.8
Nicole, A.9
Aurias, A.10
Sinet, P.M.11
Delabar, J.M.12
-
50
-
-
0028920996
-
Structure of the terminal 300 kb of DNA from human chromsome 21q
-
Reston J. T., Hu X.-L., Macina R., Spais C., Riethman H. C. Structure of the terminal 300 kb of DNA from human chromsome 21q. Genomics. 26:1995;31-38.
-
(1995)
Genomics
, vol.26
, pp. 31-38
-
-
Reston, J.T.1
Hu, X.-L.2
Macina, R.3
Spais, C.4
Riethman, H.C.5
-
51
-
-
0025339588
-
A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones
-
Riley J., Butler R., Ogilvie D., Finniear R., Jenner D., Powell S., Anand R., Smith J. C., Markham A. F. A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones. Nucleic Acids Res. 18:1990;2887-2890.
-
(1990)
Nucleic Acids Res.
, vol.18
, pp. 2887-2890
-
-
Riley, J.1
Butler, R.2
Ogilvie, D.3
Finniear, R.4
Jenner, D.5
Powell, S.6
Anand, R.7
Smith, J.C.8
Markham, A.F.9
-
52
-
-
0032521176
-
Identification and characterization of two putative human arginine methyltransferases (HRMT1L1 and HRMT1L2)
-
Scott H. S., Antonarakis S. E., Lalioti M. D., Rossier C., Silver P. A., Henry M. F. Identification and characterization of two putative human arginine methyltransferases (HRMT1L1 and HRMT1L2). Genomics. 1998.
-
(1998)
Genomics
-
-
Scott, H.S.1
Antonarakis, S.E.2
Lalioti, M.D.3
Rossier, C.4
Silver, P.A.5
Henry, M.F.6
-
53
-
-
0031915061
-
Characterization of a novel gene, C21orf2, on human chromosome 21q22.3 and its exclusion as the APECED gene by mutation analysis
-
Scott H. S., Kyriakou D. S., Peterson P., Heino M., Tähtinen M., Krohn K., Chen H., Rossier C., Lalioti M. D., Antonarakis S. E. Characterization of a novel gene, C21orf2, on human chromosome 21q22.3 and its exclusion as the APECED gene by mutation analysis. Genomics. 47:1998;64-70.
-
(1998)
Genomics
, vol.47
, pp. 64-70
-
-
Scott, H.S.1
Kyriakou, D.S.2
Peterson, P.3
Heino, M.4
Tähtinen, M.5
Krohn, K.6
Chen, H.7
Rossier, C.8
Lalioti, M.D.9
Antonarakis, S.E.10
-
54
-
-
0029977272
-
A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3
-
Sertié A. L., Quimby M., Moreira E. S., Murray J., Zatz M., Antonarakis S. E., Passos-Bueno M. R. A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3. Hum. Mol. Genet. 5:1996;843-847.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 843-847
-
-
Sertié, A.L.1
Quimby, M.2
Moreira, E.S.3
Murray, J.4
Zatz, M.5
Antonarakis, S.E.6
Passos-Bueno, M.R.7
-
55
-
-
0029057946
-
Report of the Fifth International Workshop on Human Chromosome 21 Mapping 1994
-
Shimizu N., Antonarakis S. E., Van Broeckhoven C., Patterson D., Gardiner K., Nizetic D., Créau N., Delabar J.-M., Korenberg R., Reeves R., Doering A., Chakravarti A., Minoshima S., Ritter O., Cutichia J. Report of the Fifth International Workshop on Human Chromosome 21 Mapping 1994. Cytogenet. Cell Genet. 70:1995;148-164.
-
(1995)
Cytogenet. Cell Genet.
, vol.70
, pp. 148-164
-
-
Shimizu, N.1
Antonarakis, S.E.2
Van Broeckhoven, C.3
Patterson, D.4
Gardiner, K.5
Nizetic, D.6
Créau, N.7
Delabar, J.-M.8
Korenberg, R.9
Reeves, R.10
Doering, A.11
Chakravarti, A.12
Minoshima, S.13
Ritter, O.14
Cutichia, J.15
-
56
-
-
0026703169
-
Cloning and stable maintenance of 300-kilobase-pair fragments of human DNA inEscherichia coli
-
Shizuya H., Birren B., Kim U.-J., Mancino V., Slepak T., Tachiri Y., Simon M. Cloning and stable maintenance of 300-kilobase-pair fragments of human DNA inEscherichia coli. Proc. Natl. Acad. Sci. USA. 89:1992;9794-8797.
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 9794-8797
-
-
Shizuya, H.1
Birren, B.2
Kim, U.-J.3
Mancino, V.4
Slepak, T.5
Tachiri, Y.6
Simon, M.7
-
57
-
-
0031081694
-
Two-locus admixture linkage analysis of bipolar and unipolar affective disorder supports the presence of susceptibility loci on chromosome 11p15 and 21q22
-
Smyth C., Kalsi G., Curtis D., Brynjolfsson J., O'Neill J., Rifkin L., Moloney E., Murphy P., Petursson H., Gurling H. Two-locus admixture linkage analysis of bipolar and unipolar affective disorder supports the presence of susceptibility loci on chromosome 11p15 and 21q22. Genomics. 39:1997;271-278.
-
(1997)
Genomics
, vol.39
, pp. 271-278
-
-
Smyth, C.1
Kalsi, G.2
Curtis, D.3
Brynjolfsson, J.4
O'Neill, J.5
Rifkin, L.6
Moloney, E.7
Murphy, P.8
Petursson, H.9
Gurling, H.10
-
58
-
-
0028909271
-
Cosmid assembly and anchoring to human chromosome 21
-
Soeda E., Hou D-X., Osoegawa K., Atsuchi Y., Yamagata T., Shimokawa T., Kishida H., Soeda E., Okano S., Chumakov I., Cohen D., Raff M., Gardiner K., Graw S. L., Patterson D., De Jong P., Ashworth L. K., Slezak T., Carrano A. V. Cosmid assembly and anchoring to human chromosome 21. Genomics. 25:1995;73-84.
-
(1995)
Genomics
, vol.25
, pp. 73-84
-
-
Soeda, E.1
Hou, D.-X.2
Osoegawa, K.3
Atsuchi, Y.4
Yamagata, T.5
Shimokawa, T.6
Kishida, H.7
Soeda, E.8
Okano, S.9
Chumakov, I.10
Cohen, D.11
Raff, M.12
Gardiner, K.13
Graw, S.L.14
Patterson, D.15
De Jong, P.16
Ashworth, L.K.17
Slezak, T.18
Carrano, A.V.19
-
59
-
-
19144369837
-
Construction of a 750-kb bacterial contig and restriction map in the region of human chromosome 21 containing the progressive myoclonus epilepsy gene
-
Stone N. E., Fan J.-B., Willour V., Pennacchio L. A., Warrington J. A., Hu A., de la Chapelle A., Lehesjoki A.-E., Cox D. R., Myers M. R. Construction of a 750-kb bacterial contig and restriction map in the region of human chromosome 21 containing the progressive myoclonus epilepsy gene. Genome Res. 6:1996;218-225.
-
(1996)
Genome Res.
, vol.6
, pp. 218-225
-
-
Stone, N.E.1
Fan, J.-B.2
Willour, V.3
Pennacchio, L.A.4
Warrington, J.A.5
Hu, A.6
De La Chapelle, A.7
Lehesjoki, A.-E.8
Cox, D.R.9
Myers, M.R.10
-
60
-
-
0027987228
-
A possible vulnerability locus for bipolar affective disorder on chromosome 21q22.3
-
Straub R. E., Lehner T., Luo Y., Loth J. E., Shao W., Sharpe L., Alexander J. R., Das K., Simon R., Fieve R. R., Lerer B., Endicott J., Ott J., Gilliam T. C., Baron M. A possible vulnerability locus for bipolar affective disorder on chromosome 21q22.3. Nat. Genet. 8:1994;291-296.
-
(1994)
Nat. Genet.
, vol.8
, pp. 291-296
-
-
Straub, R.E.1
Lehner, T.2
Luo, Y.3
Loth, J.E.4
Shao, W.5
Sharpe, L.6
Alexander, J.R.7
Das, K.8
Simon, R.9
Fieve, R.R.10
Lerer, B.11
Endicott, J.12
Ott, J.13
Gilliam, T.C.14
Baron, M.15
-
61
-
-
0028716950
-
Sixty new STSs (sequence-tagged sites) of human chromosome 21
-
Tanahashi H., Ito T., Hattori M., Ohira M., Ohki M., Tashiro K., Sakaki Y. Sixty new STSs (sequence-tagged sites) of human chromosome 21. DNA Res. 1:1994;85-89.
-
(1994)
DNA Res.
, vol.1
, pp. 85-89
-
-
Tanahashi, H.1
Ito, T.2
Hattori, M.3
Ohira, M.4
Ohki, M.5
Tashiro, K.6
Sakaki, Y.7
-
62
-
-
0026621632
-
Analysis of chromosome 21 yeast artificial chromosome (YAC) clones
-
Tassone F., Cheng S., Gardiner K. Analysis of chromosome 21 yeast artificial chromosome (YAC) clones. Am. J. Hum. Genet. 51:1992;1251-1264.
-
(1992)
Am. J. Hum. Genet.
, vol.51
, pp. 1251-1264
-
-
Tassone, F.1
Cheng, S.2
Gardiner, K.3
-
63
-
-
0031133949
-
Human COL6A1: Genomic characterization of the globular domains, structural and evolutionary comparison with COL6A2
-
Trikka D., Davis T., Lapenta V., Brahe C., Kessling A. M. Human COL6A1: Genomic characterization of the globular domains, structural and evolutionary comparison with COL6A2. Mamm. Genome. 8:1997;342-345.
-
(1997)
Mamm. Genome
, vol.8
, pp. 342-345
-
-
Trikka, D.1
Davis, T.2
Lapenta, V.3
Brahe, C.4
Kessling, A.M.5
-
64
-
-
0029037112
-
A provisional transcript map of the spinal muscular atrophy (SMA) critical region
-
Van der Steege G., Draaijers T. G., Grootscholten P. M., Osinga J., Anzevino R., Velonà I., Den Dunnen J-T., Scheffer H., Brahe C., van Ommen G.-J. B., Buys C. H. C. M. A provisional transcript map of the spinal muscular atrophy (SMA) critical region. Eur. J. Hum. Genet. 3:1995;87-95.
-
(1995)
Eur. J. Hum. Genet.
, vol.3
, pp. 87-95
-
-
Van Der Steege, G.1
Draaijers, T.G.2
Grootscholten, P.M.3
Osinga, J.4
Anzevino, R.5
Velonà, I.6
Den Dunnen, J.-T.7
Scheffer, H.8
Brahe, C.9
Van Ommen, G.-J.B.10
Buys, C.H.C.M.11
-
65
-
-
0030070163
-
Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from Pakistan
-
Veske A., Oehlmann R., Younus F., Mohyuddin A., Müller-Myhsok B., Mehdi S. Q., Gal A. Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from Pakistan. Hum. Mol. Genet. 5:1996;165-168.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 165-168
-
-
Veske, A.1
Oehlmann, R.2
Younus, F.3
Mohyuddin, A.4
Müller-Myhsok, B.5
Mehdi, S.Q.6
Gal, A.7
-
66
-
-
0028880529
-
Quantitative DNA fiber mapping
-
Weier H.-U. G., Wang M., Mullikin J. C., Zhu Y., Cheng J.-F., Greulich K. M., Bensimon A., Gray J. W. Quantitative DNA fiber mapping. Hum. Mol. Genet. 4:1995;1903-1910.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1903-1910
-
-
Weier, H.-U.G.1
Wang, M.2
Mullikin, J.C.3
Zhu, Y.4
Cheng, J.-F.5
Greulich, K.M.6
Bensimon, A.7
Gray, J.W.8
-
67
-
-
0023913292
-
Cloning and chromosomal localization of human genes encoding the three chains of type VI collagen
-
Weil D., Mattei M.-G., Passage E., Cong N. V., Pribula-Conway D., Mann K., Deutzman R., Timpl R., Chu M. L. Cloning and chromosomal localization of human genes encoding the three chains of type VI collagen. Am. J. Hum. Genet. 42:1988;435-445.
-
(1988)
Am. J. Hum. Genet.
, vol.42
, pp. 435-445
-
-
Weil, D.1
Mattei, M.-G.2
Passage, E.3
Cong, N.V.4
Pribula-Conway, D.5
Mann, K.6
Deutzman, R.7
Timpl, R.8
Chu, M.L.9
-
68
-
-
0029089831
-
Assignment of the human folate transporter gene to chromosome 21q22.3 by somatic cell hybrid analysis and in situ hybridization
-
Yang-Feng T. L., Ma Y. Y., Liang R., Prasad P. D., Leibach F. H., Ganapathy V. Assignment of the human folate transporter gene to chromosome 21q22.3 by somatic cell hybrid analysis and in situ hybridization. Biochem. Biophys. Res. Commun. 210:1995;874-879.
-
(1995)
Biochem. Biophys. Res. Commun.
, vol.210
, pp. 874-879
-
-
Yang-Feng, T.L.1
Ma, Y.Y.2
Liang, R.3
Prasad, P.D.4
Leibach, F.H.5
Ganapathy, V.6
-
69
-
-
0030007314
-
The human lanosterol synthase gene maps to chromosome 21q22.3
-
Young M., Chen H., Lalioti M. D., Antonarakis S. E. The human lanosterol synthase gene maps to chromosome 21q22.3. Hum. Genet. 97:1996;620-624.
-
(1996)
Hum. Genet.
, vol.97
, pp. 620-624
-
-
Young, M.1
Chen, H.2
Lalioti, M.D.3
Antonarakis, S.E.4
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