-
1
-
-
0029834510
-
Deletion of chromosome 21 in a girl with congenital hypothyroidism and mild mental retardation
-
Ahlbom B. E., Sidenvall R., Anneren G. Deletion of chromosome 21 in a girl with congenital hypothyroidism and mild mental retardation. Am. J. Med. Genet. 64:1996;501-505.
-
(1996)
Am. J. Med. Genet.
, vol.64
, pp. 501-505
-
-
Ahlbom, B.E.1
Sidenvall, R.2
Anneren, G.3
-
2
-
-
0031010599
-
Molecular origin of the mosaic sequence arrangements of higher primate alpha-globin duplication units
-
Bailey A. D., Shen C. C., Shen C. K. J. Molecular origin of the mosaic sequence arrangements of higher primate alpha-globin duplication units. Proc. Natl. Acad. Sci. USA. 94:1997;5177-5182.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 5177-5182
-
-
Bailey, A.D.1
Shen, C.C.2
Shen, C.K.J.3
-
3
-
-
0027456875
-
Clustered organization of homologous KRAB zinc-finger genes with enhanced expression in human T lymphoid cells
-
Bellefroid E. J., Marine J. C., Ried T., Lecocq P. J., Riviere M., Amemiya C., Poncelet D. A., Coulie P. G., de Jong P., Szpirer C. Clustered organization of homologous KRAB zinc-finger genes with enhanced expression in human T lymphoid cells. EMBO J. 12:1993;1363-1374.
-
(1993)
EMBO J.
, vol.12
, pp. 1363-1374
-
-
Bellefroid, E.J.1
Marine, J.C.2
Ried, T.3
Lecocq, P.J.4
Riviere, M.5
Amemiya, C.6
Poncelet, D.A.7
Coulie, P.G.8
De Jong, P.9
Szpirer, C.10
-
4
-
-
0028940587
-
Gene number, noise reduction and biological complexity
-
Bird A. P. Gene number, noise reduction and biological complexity. Trends Genet. 11:1995;94-100.
-
(1995)
Trends Genet.
, vol.11
, pp. 94-100
-
-
Bird, A.P.1
-
5
-
-
0029071146
-
Characterisation of three microsatellite polymorphisms (D21S1262, D21S1419 and D21S1421) from band 21q22.1
-
Bosch A., Guimera J., Patterson D., Estivill X. Characterisation of three microsatellite polymorphisms (D21S1262, D21S1419 and D21S1421) from band 21q22.1. Hum. Genet. 95:1995;596-598.
-
(1995)
Hum. Genet.
, vol.95
, pp. 596-598
-
-
Bosch, A.1
Guimera, J.2
Patterson, D.3
Estivill, X.4
-
7
-
-
0027470080
-
A 37-kb fragment common to the pericentromeric region of human chromosomes 13 and 21 and to the ancestral inactive centromere of chromosome 2
-
Charlieu J.-P., Laurent A. M., Orti R., Viegas-Pequinot E., Bellis M., Roizes G. A 37-kb fragment common to the pericentromeric region of human chromosomes 13 and 21 and to the ancestral inactive centromere of chromosome 2. Genomics. 15:1993;576-581.
-
(1993)
Genomics
, vol.15
, pp. 576-581
-
-
Charlieu, J.-P.1
Laurent, A.M.2
Orti, R.3
Viegas-Pequinot, E.4
Bellis, M.5
Roizes, G.6
-
8
-
-
0029010791
-
Molecular mapping of 21 features associated with partial monosomy 21: Involvement of the APP-SOD1 region
-
Chettouh Z., Croquette M.-F., Delobel B., Gilgenkrants S., Leonard C., Maunoury C., Prieur M., Rethore M.-O., Sinet P.-M., Chery M., Delabar J.-M. Molecular mapping of 21 features associated with partial monosomy 21: Involvement of the APP-SOD1 region. Am. J. Hum. Genet. 57:1995;62-71.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 62-71
-
-
Chettouh, Z.1
Croquette, M.-F.2
Delobel, B.3
Gilgenkrants, S.4
Leonard, C.5
Maunoury, C.6
Prieur, M.7
Rethore, M.-O.8
Sinet, P.-M.9
Chery, M.10
Delabar, J.-M.11
-
9
-
-
0026738541
-
Continuum of overlapping clones spanning the entire human chromosome 21q
-
Chumakov I., Rigault P., Guillou S., Ougen P., Billaut A., Guascono G., Gervy P., Legall I., Soularue P., Grinas L., Bougueleret L., Bellanne-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., Okhi 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
Guascono, G.6
Gervy, P.7
Legall, I.8
Soularue, P.9
Grinas, L.10
Bougueleret, L.11
Bellanne-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
Okhi, M.32
Le Paslier, D.33
Heilig, R.34
Antonarakis, S.35
Cohen, D.36
more..
-
10
-
-
0027345964
-
Cosmid sequencing
-
Craxton M. Cosmid sequencing. Methods Mol. Biol. 23:1993;149-167.
-
(1993)
Methods Mol. Biol.
, vol.23
, pp. 149-167
-
-
Craxton, M.1
-
11
-
-
0025280026
-
Centre d'Etude du Polymorphisme Humain (CEPH): Collaborative genetic mapping of the human genome
-
Dausset J., Cann H., Cohen D., Lathrop M., Lalouel J.-M., White R. Centre d'Etude du Polymorphisme Humain (CEPH): Collaborative genetic mapping of the human genome. Genomics. 6:1990;575-577.
-
(1990)
Genomics
, vol.6
, pp. 575-577
-
-
Dausset, J.1
Cann, H.2
Cohen, D.3
Lathrop, M.4
Lalouel, J.-M.5
White, R.6
-
12
-
-
0025776579
-
A sequence assembly and editing program for efficient management of large projects
-
Dear S., Staden R. A sequence assembly and editing program for efficient management of large projects. Nucleic Acids Res. 19:1991;3907-3911.
-
(1991)
Nucleic Acids Res.
, vol.19
, pp. 3907-3911
-
-
Dear, S.1
Staden, R.2
-
13
-
-
0028145950
-
Cloning and characterization of a 135- To 500-kb region of homology on the long arm of human chromosome 21
-
Dutriaux A., Rossier J., Van Hul W., Nizetic D., Theophille D., Delabar J. M., Van Broeckhoven C., Potier M.-C. Cloning and characterization of a 135- to 500-kb region of homology on the long arm of human chromosome 21. Genomics. 22:1994;472-477.
-
(1994)
Genomics
, vol.22
, pp. 472-477
-
-
Dutriaux, A.1
Rossier, J.2
Van Hul, W.3
Nizetic, D.4
Theophille, D.5
Delabar, J.M.6
Van Broeckhoven, C.7
Potier, M.-C.8
-
14
-
-
0030757906
-
Interchromosomal duplications of the adrenoleukodystrophy locus: A phenomenon of pericentromeric plasticity
-
Eichler E. E., Budarf M. L., Rocchi M., Deaven L. L., Doggett N. A., Baldini A., Nelson D. L., Mohrenweiser H. W. Interchromosomal duplications of the adrenoleukodystrophy locus: A phenomenon of pericentromeric plasticity. Hum. Mol. Genet. 6:1997;991-1002.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 991-1002
-
-
Eichler, E.E.1
Budarf, M.L.2
Rocchi, M.3
Deaven, L.L.4
Doggett, N.A.5
Baldini, A.6
Nelson, D.L.7
Mohrenweiser, H.W.8
-
15
-
-
8944233367
-
Duplication of a gene-rich cluster between 16p11.1 and Xq28: A novel pericentromeric-directed mechanism for paralogous genome evolution
-
Eichler E. E., Lu F., Shen Y., Antonacci R., Jurecic V., Doggett N. A., Moyzis R. K., Baldini A., Gibbs R. A., Nelson D. L. Duplication of a gene-rich cluster between 16p11.1 and Xq28: A novel pericentromeric-directed mechanism for paralogous genome evolution. Hum. Mol. Genet. 5:1996;899-912.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 899-912
-
-
Eichler, E.E.1
Lu, F.2
Shen, Y.3
Antonacci, R.4
Jurecic, V.5
Doggett, N.A.6
Moyzis, R.K.7
Baldini, A.8
Gibbs, R.A.9
Nelson, D.L.10
-
16
-
-
0020793569
-
A technique for radiolabelling DNA restriction fragments to high specific activity
-
Feinberg A. P., Vogelstein B. A technique for radiolabelling DNA restriction fragments to high specific activity. Anal. Biochem. 132:1983;6-13.
-
(1983)
Anal. Biochem.
, vol.132
, pp. 6-13
-
-
Feinberg, A.P.1
Vogelstein, B.2
-
17
-
-
0025087560
-
Human sex-chromosome-specific repeats within a region of pseudoautosomal/Yq homology
-
Fisher E. M. C., Alitalo T., Luoh S.-W., de La Chapelle A., Page D. C. Human sex-chromosome-specific repeats within a region of pseudoautosomal/Yq homology. Genomics. 7:1990;625-628.
-
(1990)
Genomics
, vol.7
, pp. 625-628
-
-
Fisher, E.M.C.1
Alitalo, T.2
Luoh, S.-W.3
De La Chapelle, A.4
Page, D.C.5
-
18
-
-
0025092046
-
Analysis of human chromosome 21: Correlation of physical and cytogenetic maps; Gene and CpG islands distribution
-
Gardiner K., Horisberger M., Kraus J., Tantravahi U., Korenberg J., Rao V., Reddy S., Patterson D. Analysis of human chromosome 21: Correlation of physical and cytogenetic maps; gene and CpG islands distribution. EMBO J. 9:1990;25-34.
-
(1990)
EMBO J.
, vol.9
, pp. 25-34
-
-
Gardiner, K.1
Horisberger, M.2
Kraus, J.3
Tantravahi, U.4
Korenberg, J.5
Rao, V.6
Reddy, S.7
Patterson, D.8
-
19
-
-
0028958458
-
When it comes to evolution, humans are in the slow class
-
Gibbons A. When it comes to evolution, humans are in the slow class. Science. 267:1995;1907-1908.
-
(1995)
Science
, vol.267
, pp. 1907-1908
-
-
Gibbons, A.1
-
20
-
-
0031944798
-
Bacterial contig map of the 21q11 region associated with Alzheimer's disease and abnormal myelopoiesis in Down syndrome
-
Groet J., Ives J. H., South A. P., Baptista P. R., Jones T. A., Yaspo M.-L., Lehrach H., Potier M.-C., Van Broeckhoven C., Nizetic D. Bacterial contig map of the 21q11 region associated with Alzheimer's disease and abnormal myelopoiesis in Down syndrome. Genome Res. 8:1998;385-398.
-
(1998)
Genome Res.
, vol.8
, pp. 385-398
-
-
Groet, J.1
Ives, J.H.2
South, A.P.3
Baptista, P.R.4
Jones, T.A.5
Yaspo, M.-L.6
Lehrach, H.7
Potier, M.-C.8
Van Broeckhoven, C.9
Nizetic, D.10
-
21
-
-
0020639078
-
Unusual evolutionary conservation and frequent DNA segment exchange in class I genes of the major histocompatibility complex
-
Hayashida H., Miyata T. Unusual evolutionary conservation and frequent DNA segment exchange in class I genes of the major histocompatibility complex. Proc. Natl. Acad. Sci. USA. 80:1983;2671-2675.
-
(1983)
Proc. Natl. Acad. Sci. USA
, vol.80
, pp. 2671-2675
-
-
Hayashida, H.1
Miyata, T.2
-
22
-
-
0028318417
-
A new bacteriophage P1-derived vector for the propagation of large human DNA fragments
-
Ioannou P. A., Amemiya C. T., Garnes J., Kroisel P. M., Shizuya H., Chen C., Batzer M. A., de Jong P. J. A new bacteriophage P1-derived vector for the propagation 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
Shizuya, H.5
Chen, C.6
Batzer, M.A.7
De Jong, P.J.8
-
23
-
-
0027278118
-
A chromosome 13-specific human satellite I DNA subfamily with minor presence on chromosome 21: Further studies on robertsonian translocations
-
Kalitsis P., Earle E., Vissel B., Shaffer L. G., Cho A. A chromosome 13-specific human satellite I DNA subfamily with minor presence on chromosome 21: Further studies on robertsonian translocations. Genomics. 16:1993;104-112.
-
(1993)
Genomics
, vol.16
, pp. 104-112
-
-
Kalitsis, P.1
Earle, E.2
Vissel, B.3
Shaffer, L.G.4
Cho, A.5
-
24
-
-
0025780858
-
Deletion of chromosome 21 and normal intelligence: Molecular definition of the lesion
-
Korenberg J. R., Kalousek D. K., Anneren G., Pulst S. M., Hall J. G., Epstein C. J., Cox D. R. Deletion of chromosome 21 and normal intelligence: Molecular definition of the lesion. Hum. Genet. 87:1991;112-118.
-
(1991)
Hum. Genet.
, vol.87
, pp. 112-118
-
-
Korenberg, J.R.1
Kalousek, D.K.2
Anneren, G.3
Pulst, S.M.4
Hall, J.G.5
Epstein, C.J.6
Cox, D.R.7
-
26
-
-
0030906761
-
Clone-contig and STS maps of the hereditary hemochromatosis region on human chromosome 6p21.3-p22
-
Lauer P., Meyer N. C., Prass C. E., Starnes S. M., Wolff R. K., Gnirke A. Clone-contig and STS maps of the hereditary hemochromatosis region on human chromosome 6p21.3-p22. Genome Res. 7:1997;457-470.
-
(1997)
Genome Res.
, vol.7
, pp. 457-470
-
-
Lauer, P.1
Meyer, N.C.2
Prass, C.E.3
Starnes, S.M.4
Wolff, R.K.5
Gnirke, A.6
-
27
-
-
0027284770
-
Evolution of the vertebrate genome as reflected in paralogous chromosomal regions in man and the house mouse
-
Lundin L. G. Evolution of the vertebrate genome as reflected in paralogous chromosomal regions in man and the house mouse. Genomics. 16:1993;1-19.
-
(1993)
Genomics
, vol.16
, pp. 1-19
-
-
Lundin, L.G.1
-
28
-
-
0028979816
-
Structure of the human CRFB4 gene: Comparison with its IFNAR neighbor
-
Lutfalla G., McInnis M. G., Antonarakis S. E., Uze G. Structure of the human CRFB4 gene: Comparison with its IFNAR neighbor. J. Mol. Evol. 41:1995;338-344.
-
(1995)
J. Mol. Evol.
, vol.41
, pp. 338-344
-
-
Lutfalla, G.1
McInnis, M.G.2
Antonarakis, S.E.3
Uze, G.4
-
29
-
-
0026345290
-
Construction, arraying and high-density screening of large insert libraries from human chromosome X and 21: Their potential use as reference libraries
-
Nizetic D., Zehetner G., Monaco A. P., Gellen L., Young B. D., Lehrach H. Construction, arraying and high-density screening of large insert libraries from human chromosome X and 21: Their potential use as reference libraries. Proc. Natl. Acad. Sci. USA. 88:1991;3233-3237.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 3233-3237
-
-
Nizetic, D.1
Zehetner, G.2
Monaco, A.P.3
Gellen, L.4
Young, B.D.5
Lehrach, H.6
-
30
-
-
0028231476
-
An integrated YAC-overlap and "cosmid-pocket" of the human chromosome 21
-
Nizetic D., Gellen L., Hamvas R., Mott R., Grigoriev A., Vatcheva R., Zehetner G., Yaspo M.-L., Dutriaux A., Lopes C., Delabar J. M., Van Broeckhoven C., Potier M-C., Lehrach H. An integrated YAC-overlap and "cosmid-pocket" of the human chromosome 21. Hum. Mol. Genet. 3:1994;759-770.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 759-770
-
-
Nizetic, D.1
Gellen, L.2
Hamvas, R.3
Mott, R.4
Grigoriev, A.5
Vatcheva, R.6
Zehetner, G.7
Yaspo, M.-L.8
Dutriaux, A.9
Lopes, C.10
Delabar, J.M.11
Van Broeckhoven, C.12
Potier, M-C.13
Lehrach, H.14
-
31
-
-
19144363132
-
Isolation of a cosmid clone corresponding to an inv(21) breakpoint of a patient with transient abnormal myelopoiesis
-
Ohta T., Nakano M., Tsujita T., Abe K., Osoegawa K., Yamagata T., Yoshiura K., Jinno Y., Soeda E., Nakamura Y., Niikawa N. Isolation of a cosmid clone corresponding to an inv(21) breakpoint of a patient with transient abnormal myelopoiesis. Am. J. Hum. Genet. 58:1996;544-550.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 544-550
-
-
Ohta, T.1
Nakano, M.2
Tsujita, T.3
Abe, K.4
Osoegawa, K.5
Yamagata, T.6
Yoshiura, K.7
Jinno, Y.8
Soeda, E.9
Nakamura, Y.10
Niikawa, N.11
-
32
-
-
0031194665
-
High-resolution physical mapping of a 6.7-Mb YAC contig spanning a region critical for the monosomy 21 phenotype in 21q21.3-q22.1
-
Orti R., Mégarbane A., Maunoury C., Van Broeckhoven C., Sinet P.-M., Delabar J. M. High-resolution physical mapping of a 6.7-Mb YAC contig spanning a region critical for the monosomy 21 phenotype in 21q21.3-q22.1. Genomics. 43:1997;25-33.
-
(1997)
Genomics
, vol.43
, pp. 25-33
-
-
Orti, R.1
Mégarbane, A.2
Maunoury, C.3
Van Broeckhoven, C.4
Sinet, P.-M.5
Delabar, J.M.6
-
33
-
-
0025425540
-
Linkage analysis of the human HGM14 gene on chromosome 21 using a dinucleotide repeat as polymorphic marker
-
Petersen M. B., Economou E. P., Slaugenhaupt S. A., Chakravarti A., Antonarakis S. E. Linkage analysis of the human HGM14 gene on chromosome 21 using a dinucleotide repeat as polymorphic marker. Genomics. 7:1990;136-138.
-
(1990)
Genomics
, vol.7
, pp. 136-138
-
-
Petersen, M.B.1
Economou, E.P.2
Slaugenhaupt, S.A.3
Chakravarti, A.4
Antonarakis, S.E.5
-
34
-
-
0026460307
-
Construction and characterization of a yeast artificial chromosome library containing 1.5 equivalents of human chromosome 21
-
Potier M.-C., Kuo W. L., Dutriaux A., Gray J., Goedert M. Construction and characterization of a yeast artificial chromosome library containing 1.5 equivalents of human chromosome 21. Genomics. 14:1992;481-483.
-
(1992)
Genomics
, vol.14
, pp. 481-483
-
-
Potier, M.-C.1
Kuo, W.L.2
Dutriaux, A.3
Gray, J.4
Goedert, M.5
-
35
-
-
0029678618
-
Use of YAC fragmentation to delimit a duplicated region on human chromosome 21
-
Potier M.-C., Dutriaux A., Reeves R. Use of YAC fragmentation to delimit a duplicated region on human chromosome 21. Mamm. Genome. 7:1996;85-88.
-
(1996)
Mamm. Genome.
, vol.7
, pp. 85-88
-
-
Potier, M.-C.1
Dutriaux, A.2
Reeves, R.3
-
36
-
-
0031022190
-
Emergence and scattering of multiple neurofibromatosis (NF1)-related sequences during hominoid evolution suggest a process of pericentromeric interchromosomal transposition
-
Régnier V., Meddeb M., Lecointre G., Richard F., Duverger A., Nguyen V. C., Dutrillaux B., Bernheim A., Danglot G. Emergence and scattering of multiple neurofibromatosis (NF1)-related sequences during hominoid evolution suggest a process of pericentromeric interchromosomal transposition. Hum. Mol Genet. 6:1997;9-16.
-
(1997)
Hum. Mol Genet.
, vol.6
, pp. 9-16
-
-
Régnier, V.1
Meddeb, M.2
Lecointre, G.3
Richard, F.4
Duverger, A.5
Nguyen, V.C.6
Dutrillaux, B.7
Bernheim, A.8
Danglot, G.9
-
37
-
-
0025339588
-
A novel, rapid method for the isolation of terminal sequence 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 sequence 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
-
38
-
-
0025280887
-
A familial interstitial deletion of the long arm of chromosome 21
-
Roland B., Cox D. M., Fowlow S. B., Robertson A. S. A familial interstitial deletion of the long arm of chromosome 21. Clin. Genet. 37:1990;423-428.
-
(1990)
Clin. Genet.
, vol.37
, pp. 423-428
-
-
Roland, B.1
Cox, D.M.2
Fowlow, S.B.3
Robertson, A.S.4
-
39
-
-
0011104563
-
Isolation of chromosome 21 encoded expressed sequences
-
Stuyver L., Van Camp G., Van De Voorde A., Van Broeckhoven C., Van Heuverswyn H. Isolation of chromosome 21 encoded expressed sequences. Cytogenet. Cell. Genet. 58:1991;2039-2040.
-
(1991)
Cytogenet. Cell. Genet.
, vol.58
, pp. 2039-2040
-
-
Stuyver, L.1
Van Camp, G.2
Van De Voorde, A.3
Van Broeckhoven, C.4
Van Heuverswyn, H.5
-
40
-
-
0026589929
-
Unique sequence homology in the pericentromeric regions of the long arm of chromosome 13 and 21 DNA
-
Van Camp G., Cruts M., Backhovens H., Wehnert A., Stinissen P., Van Broeckhoven C. Unique sequence homology in the pericentromeric regions of the long arm of chromosome 13 and 21 DNA. Genomics. 12:1992;158-160.
-
(1992)
Genomics
, vol.12
, pp. 158-160
-
-
Van Camp, G.1
Cruts, M.2
Backhovens, H.3
Wehnert, A.4
Stinissen, P.5
Van Broeckhoven, C.6
-
41
-
-
0027506362
-
A contiguous physical map of the pericentromeric region of chromosome 21 between D21Z1 and D21S13E
-
Van Hul W., Van Camp G., Stuyver L., Delabar J. M., McInnis M. G., Warren C. A., Antonarakis S. E., Van Broeckhoven C. A contiguous physical map of the pericentromeric region of chromosome 21 between D21Z1 and D21S13E. Genomics. 15:1993;626-630.
-
(1993)
Genomics
, vol.15
, pp. 626-630
-
-
Van Hul, W.1
Van Camp, G.2
Stuyver, L.3
Delabar, J.M.4
McInnis, M.G.5
Warren, C.A.6
Antonarakis, S.E.7
Van Broeckhoven, C.8
-
42
-
-
0029931203
-
DOP-vector PCR: A method for rapid isolation and sequencing of insert termini from PAC clones
-
Wu C., Zhu S., Simpson S., de Jong P. J. DOP-vector PCR: A method for rapid isolation and sequencing of insert termini from PAC clones. Nucleic Acids Res. 24:1996;2614-2615.
-
(1996)
Nucleic Acids Res
, vol.24
, pp. 2614-2615
-
-
Wu, C.1
Zhu, S.2
Simpson, S.3
De Jong, P.J.4
-
43
-
-
0025231729
-
Transposition of human immunoglobulin V&kappa: Genes within the same chromosome and the mechanism of their amplification
-
Zimmer F.-J., Hameister H., Schek H., Zachau H. G. Transposition of human immunoglobulin V&kappa: Genes within the same chromosome and the mechanism of their amplification. EMBO J. 9:1990;1535-1542.
-
(1990)
EMBO J.
, vol.9
, pp. 1535-1542
-
-
Zimmer, F.-J.1
Hameister, H.2
Schek, H.3
Zachau, H.G.4
-
44
-
-
0030589502
-
Identification of new members of the Gas2 and Ras families in the 22q12 chromosome region
-
Zucman-Rossi J., Legoix P., Thomas G. Identification of new members of the Gas2 and Ras families in the 22q12 chromosome region. Genomics. 38:1996;247-254.
-
(1996)
Genomics
, vol.38
, pp. 247-254
-
-
Zucman-Rossi, J.1
Legoix, P.2
Thomas, G.3
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