-
1
-
-
0019967273
-
Genetic homology and crossing over in the X and Y chromosomes of mammals
-
Burgoyne, P.S. (1982) Genetic homology and crossing over in the X and Y chromosomes of mammals. Hum. Genet., 61, 85-90.
-
(1982)
Hum. Genet.
, vol.61
, pp. 85-90
-
-
Burgoyne, P.S.1
-
2
-
-
0025248381
-
Deletion of the pseudoautosomal region and lack of sex chromosome pairing at pachytene in two infertile men carrying an X;Y translocation
-
Gabriel-Robez, O., Ratomponirina, C., Dutrillaux, B., Carré-Pigeon, F. and Rumpler, Y. (1990) Deletion of the pseudoautosomal region and lack of sex chromosome pairing at pachytene in two infertile men carrying an X;Y translocation. Cytogenet. Cell Genet., 54, 39-42.
-
(1990)
Cytogenet. Cell Genet.
, vol.54
, pp. 39-42
-
-
Gabriel-Robez, O.1
Ratomponirina, C.2
Dutrillaux, B.3
Carré-Pigeon, F.4
Rumpler, Y.5
-
3
-
-
0026658839
-
Role of the pseudoautosomal region in sex-chromosome pairing during male meiosis: Meiotic studies in a man with deletion of distal Xp
-
Mohandas, T.K., Speed, R.M., Passage, M.B., Yen, P.H., Chandley, A.C. and Shapiro, L.J. (1992) Role of the pseudoautosomal region in sex-chromosome pairing during male meiosis: meiotic studies in a man with deletion of distal Xp. Am. J. Hum. Genet., 51, 526-533.
-
(1992)
Am. J. Hum. Genet.
, vol.51
, pp. 526-533
-
-
Mohandas, T.K.1
Speed, R.M.2
Passage, M.B.3
Yen, P.H.4
Chandley, A.C.5
Shapiro, L.J.6
-
4
-
-
0026456696
-
Fertility in mice requires X-Y pairing and a Y-chromosomal 'spermiogenesis' gene mapping to the long arm
-
Burgoyne, P.S., Mahadevaiah, S.K., Sutcliffe, M.J. and Palmer, S.J. (1992) Fertility in mice requires X-Y pairing and a Y-chromosomal 'spermiogenesis' gene mapping to the long arm. Cell, 71, 391-398.
-
(1992)
Cell
, vol.71
, pp. 391-398
-
-
Burgoyne, P.S.1
Mahadevaiah, S.K.2
Sutcliffe, M.J.3
Palmer, S.J.4
-
5
-
-
0027437257
-
The pseudoautosomal regions of the human sex chromosomes
-
Rappold, G.A. (1993) The pseudoautosomal regions of the human sex chromosomes. Hum. Genet., 92, 315-324.
-
(1993)
Hum. Genet.
, vol.92
, pp. 315-324
-
-
Rappold, G.A.1
-
6
-
-
0023598410
-
Identification of incomplete coding sequences for steroid sulphatase on the human Y chromosome: Evidence for an ancestral pseudoautosomal gene?
-
Fraser, N., Ballabio, A., Zollo, M., Persico, G. and Craig, I.W. (1987) Identification of incomplete coding sequences for steroid sulphatase on the human Y chromosome: evidence for an ancestral pseudoautosomal gene? Development, 101 (suppl.), 127-132.
-
(1987)
Development
, vol.101
, Issue.SUPPL.
, pp. 127-132
-
-
Fraser, N.1
Ballabio, A.2
Zollo, M.3
Persico, G.4
Craig, I.W.5
-
7
-
-
0024208474
-
The human X-linked steroid sulfatase gene and a Y-encoded pseudogene: Evidence for an inversion of the Y chromosome during primate evolution
-
Yen, P.H., Marsh, B., Allen, E., Tsai, S.P., Ellison, J., Connolly, L., Neiswanger, K. and Shapiro, L.J. (1988) The human X-linked steroid sulfatase gene and a Y-encoded pseudogene: evidence for an inversion of the Y chromosome during primate evolution. Cell, 55, 1123-1135.
-
(1988)
Cell
, vol.55
, pp. 1123-1135
-
-
Yen, P.H.1
Marsh, B.2
Allen, E.3
Tsai, S.P.4
Ellison, J.5
Connolly, L.6
Neiswanger, K.7
Shapiro, L.J.8
-
8
-
-
0024843575
-
The mammalian pseudo-autosomal region
-
Ellis, N.A. and Goodfellow, P.N. (1989) The mammalian pseudo-autosomal region. Trends Genet., 5, 406-410.
-
(1989)
Trends Genet.
, vol.5
, pp. 406-410
-
-
Ellis, N.A.1
Goodfellow, P.N.2
-
9
-
-
0025938481
-
A gene deleted in Kallman's syndrome shares homology with neural cell adhesion and axonal pathfinding molecules
-
Franco, B., Guioli, S., Pragliola, A., Incerti, B., Bardoni, B., Tonlorenzi, R., Carrozzo, R., Maestrini, E., Pieretti, M., Taillon-Miller, P., Brown, C.J., Willard, H.F., Lawrence, C., Persico, M.G., Camerino, G. and Ballabio, A. (1991) A gene deleted in Kallman's syndrome shares homology with neural cell adhesion and axonal pathfinding molecules. Nature, 353, 529-536.
-
(1991)
Nature
, vol.353
, pp. 529-536
-
-
Franco, B.1
Guioli, S.2
Pragliola, A.3
Incerti, B.4
Bardoni, B.5
Tonlorenzi, R.6
Carrozzo, R.7
Maestrini, E.8
Pieretti, M.9
Taillon-Miller, P.10
Brown, C.J.11
Willard, H.F.12
Lawrence, C.13
Persico, M.G.14
Camerino, G.15
Ballabio, A.16
-
10
-
-
0027021440
-
Structure of the X-linked Kallmann syndrome gene and its homologous pseudogene on the Y chromosome
-
del Castillo, J., Cohen-Salmon, M., Blanchard, S., Lutfalla, G. and Petit, C. (1992) Structure of the X-linked Kallmann syndrome gene and its homologous pseudogene on the Y chromosome. Nature Genet., 2, 305-310.
-
(1992)
Nature Genet.
, vol.2
, pp. 305-310
-
-
Del Castillo, J.1
Cohen-Salmon, M.2
Blanchard, S.3
Lutfalla, G.4
Petit, C.5
-
11
-
-
0027021441
-
Kallmann syndrome gene on the X and Y chromosomes: Implications for evolutionary divergence of human sex chromosomes
-
Incerti, B., Guioli, S., Pragliola, A., Zanaria, E., Borsani, G., Tonlorenzi, R., Bardoni, B., Franco, B., Wheeeler, D., Ballabio, A. and Camerino, G. (1992) Kallmann syndrome gene on the X and Y chromosomes: implications for evolutionary divergence of human sex chromosomes. Nature Genet., 2, 311-314.
-
(1992)
Nature Genet.
, vol.2
, pp. 311-314
-
-
Incerti, B.1
Guioli, S.2
Pragliola, A.3
Zanaria, E.4
Borsani, G.5
Tonlorenzi, R.6
Bardoni, B.7
Franco, B.8
Wheeeler, D.9
Ballabio, A.10
Camerino, G.11
-
12
-
-
0029003706
-
The human protein kinase gene PKX1 on Xp22.3 displays Xp/YP homology and is a site of chromosomal instability
-
Klink, A., Schiebel, K., Winkelmann, M., Rao, E., Horthemke, B., Lüdecke, H.J., Claussen, U., Scherer, G. and Rappold, G.A. (1995) The human protein kinase gene PKX1 on Xp22.3 displays Xp/YP homology and is a site of chromosomal instability. Hum. Mol. Genet., 4, 869-878.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 869-878
-
-
Klink, A.1
Schiebel, K.2
Winkelmann, M.3
Rao, E.4
Horthemke, B.5
Lüdecke, H.J.6
Claussen, U.7
Scherer, G.8
Rappold, G.A.9
-
13
-
-
0029987932
-
Characterization of a cluster of sulfatase genes on Xp22.3 suggests gene duplications in an ancestral pseudoautosomal region
-
Meroni, G., Franco, B., Archidiacono, N., Messali, S., Andolfi, G., Rocchi, M. and Ballabio, A. (1996) Characterization of a cluster of sulfatase genes on Xp22.3 suggests gene duplications in an ancestral pseudoautosomal region. Hum. Mol. Genet., 5, 423-431.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 423-431
-
-
Meroni, G.1
Franco, B.2
Archidiacono, N.3
Messali, S.4
Andolfi, G.5
Rocchi, M.6
Ballabio, A.7
-
14
-
-
8544275793
-
Comparative mapping of Xp22 genes in hominoids - Evolutionary linear instability of their Y homologues
-
Gläser, B., Grützner, F., Taylor, K., Schiebel, K., Meroni, G., Tsioupra, K., Pasantes, J., Rietschel, W., Toder, R., Willmann, U., Zeitler, S., Yen, P., Ballabio, A., Rappold, G. and Schempp, W. (1997) Comparative mapping of Xp22 genes in hominoids - evolutionary linear instability of their Y homologues. Chromosome Res., 5, 167-176.
-
(1997)
Chromosome Res.
, vol.5
, pp. 167-176
-
-
Gläser, B.1
Grützner, F.2
Taylor, K.3
Schiebel, K.4
Meroni, G.5
Tsioupra, K.6
Pasantes, J.7
Rietschel, W.8
Toder, R.9
Willmann, U.10
Zeitler, S.11
Yen, P.12
Ballabio, A.13
Rappold, G.14
Schempp, W.15
-
15
-
-
15644383347
-
Simian Y chromosomes: Species-specific rearrangements of DAZ, RBM, and TSPY versus contiguity of PAR and SRY
-
Gläser, B., Grützner, F., Willmann, U., Stanyon, R., Arnold, N., Taylor, K., Rietschel, W., Zeitler, S., Toder, R. and Schempp, W. (1998) Simian Y chromosomes: species-specific rearrangements of DAZ, RBM, and TSPY versus contiguity of PAR and SRY. Mamm. Genome, 9, 226-231.
-
(1998)
Mamm. Genome
, vol.9
, pp. 226-231
-
-
Gläser, B.1
Grützner, F.2
Willmann, U.3
Stanyon, R.4
Arnold, N.5
Taylor, K.6
Rietschel, W.7
Zeitler, S.8
Toder, R.9
Schempp, W.10
-
16
-
-
0031695696
-
Evolution of chromosome Y in primates
-
Archidiacono, N., Storlazzi, C.T., Spalluto, C., Ricco, A.S., Marzella, R. and Rocchi, M. (1998) Evolution of chromosome Y in primates. Chromosoma, 107, 241-246.
-
(1998)
Chromosoma
, vol.107
, pp. 241-246
-
-
Archidiacono, N.1
Storlazzi, C.T.2
Spalluto, C.3
Ricco, A.S.4
Marzella, R.5
Rocchi, M.6
-
17
-
-
0030793893
-
Genes located in and near the human pseudoautosomal region are located in the X-Y pairing region in dog and sheep
-
Toder, R., Gläser, B., Schiebel, K., Wilcox, S.A., Rappold, G., Graves, J.A.M. and Schempp, W. (1997) Genes located in and near the human pseudoautosomal region are located in the X-Y pairing region in dog and sheep. Chromosome Res., 5, 301-306.
-
(1997)
Chromosome Res.
, vol.5
, pp. 301-306
-
-
Toder, R.1
Gläser, B.2
Schiebel, K.3
Wilcox, S.A.4
Rappold, G.5
Graves, J.A.M.6
Schempp, W.7
-
18
-
-
0033000596
-
Localization and characterization of nucleotide sequences from the canine Y chromosome
-
Olivier, M., Breen, M., Binns, M.M. and Lust, G. (1999) Localization and characterization of nucleotide sequences from the canine Y chromosome. Chromosome Res., 7, 223-233.
-
(1999)
Chromosome Res.
, vol.7
, pp. 223-233
-
-
Olivier, M.1
Breen, M.2
Binns, M.M.3
Lust, G.4
-
19
-
-
0009104892
-
Mapping of the sheep and goat Sry genes to the long arms of the Y chromosomes by the FISH method
-
Cui, X., Kato, Y., Sato, S. and Sutou, S. (1996) Mapping of the sheep and goat Sry genes to the long arms of the Y chromosomes by the FISH method. Anim. Sci. Technol. (Jpn), 67, 333-337.
-
(1996)
Anim. Sci. Technol. (Jpn)
, vol.67
, pp. 333-337
-
-
Cui, X.1
Kato, Y.2
Sato, S.3
Sutou, S.4
-
20
-
-
0028890217
-
ANT3 and STS are autosomal in prosimian lemurs: Implications for the evolution of the pseudoautosomal region
-
Toder, R., Rappold, G.A., Schiebel, K. and Schempp, W. (1995) ANT3 and STS are autosomal in prosimian lemurs: implications for the evolution of the pseudoautosomal region. Hum. Genet., 95, 22-28.
-
(1995)
Hum. Genet.
, vol.95
, pp. 22-28
-
-
Toder, R.1
Rappold, G.A.2
Schiebel, K.3
Schempp, W.4
-
21
-
-
0026907357
-
The human GM-CSF receptor subunit gene is autosomal in mouse
-
Distèche, M.C., Brannan, C.J., Larsen, A., Adler, A., Schorderet, D.F., Gearing, D., Copeland, N.G., Jenkins, N.A. and Park, L.S. (1992) The human GM-CSF receptor subunit gene is autosomal in mouse. Nature Genet., 1, 333-336.
-
(1992)
Nature Genet.
, vol.1
, pp. 333-336
-
-
Distèche, M.C.1
Brannan, C.J.2
Larsen, A.3
Adler, A.4
Schorderet, D.F.5
Gearing, D.6
Copeland, N.G.7
Jenkins, N.A.8
Park, L.S.9
-
22
-
-
0027332386
-
Gene for the alpha-subunit of the human interleukin-3 receptor (IL3RA) localized to the X-Y pseudoautosomal region
-
Milatovich, A., Kitamura, T., Miyajima, A. and Francke, U. (1993) Gene for the alpha-subunit of the human interleukin-3 receptor (IL3RA) localized to the X-Y pseudoautosomal region. Am. J. Hum. Genet., 53, 1146-1153.
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 1146-1153
-
-
Milatovich, A.1
Kitamura, T.2
Miyajima, A.3
Francke, U.4
-
23
-
-
0031788775
-
The origin and evolution of the pseudoautosomal regions of human sex chromosomes
-
Graves, J.A.M., Wakefield, M.J. and Toder, R. (1998) The origin and evolution of the pseudoautosomal regions of human sex chromosomes. Hum. Mol. Genet., 7, 1991-1996.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1991-1996
-
-
Graves, J.A.M.1
Wakefield, M.J.2
Toder, R.3
-
24
-
-
0030801002
-
Gapped BLAST and PSI-BLAST: A new generation of protein database search programs
-
Altschul, S.F., Madden, T.L., Schäffer, A.A., Zhang, J., Zhan, Z., Miller, W. and Lipman, D.F. (1997) Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res., 25, 3389-3402.
-
(1997)
Nucleic Acids Res.
, vol.25
, pp. 3389-3402
-
-
Altschul, S.F.1
Madden, T.L.2
Schäffer, A.A.3
Zhang, J.4
Zhan, Z.5
Miller, W.6
Lipman, D.F.7
-
25
-
-
0018350528
-
Synaptonemal complex analysis of heteromorphic bivalents in Lemur hybrids
-
Moses, M.J., Karatsis, P.A. and Hamilton, A.E. (1979) Synaptonemal complex analysis of heteromorphic bivalents in Lemur hybrids. Chromosoma, 70, 141-160.
-
(1979)
Chromosoma
, vol.70
, pp. 141-160
-
-
Moses, M.J.1
Karatsis, P.A.2
Hamilton, A.E.3
-
26
-
-
0018427309
-
Chromosomal evolution in primates: Tentative phylogeny from Microcebus murinus (Prosimian) to man
-
Dutrillaux, B. (1979) Chromosomal evolution in primates: tentative phylogeny from Microcebus murinus (Prosimian) to man. Hum. Genet., 48, 251-314.
-
(1979)
Hum. Genet.
, vol.48
, pp. 251-314
-
-
Dutrillaux, B.1
-
27
-
-
0024394342
-
Mammalian sex-chromosome evolution: A conserved homologous segment on X and Y chromosomes in primates
-
Schempp, W., Weber, B. and Müller, G. (1989) Mammalian sex-chromosome evolution: a conserved homologous segment on X and Y chromosomes in primates. Cytogenet. Cell Genet., 50, 201-205.
-
(1989)
Cytogenet. Cell Genet.
, vol.50
, pp. 201-205
-
-
Schempp, W.1
Weber, B.2
Müller, G.3
-
28
-
-
0027306801
-
Rapid sequence evolution of the mammalian sex-determining gene SRY
-
Whitfield, L.S., Lovell-Badge, R. and Goodfellow, P.N. (1993) Rapid sequence evolution of the mammalian sex-determining gene SRY. Nature, 364, 713-715.
-
(1993)
Nature
, vol.364
, pp. 713-715
-
-
Whitfield, L.S.1
Lovell-Badge, R.2
Goodfellow, P.N.3
-
29
-
-
0023506818
-
DNA hybridization evidence of hominoid phylogeny: Results from an expanded data set
-
Sibley, C.G. and Ahlquist, J.E. (1987) DNA hybridization evidence of hominoid phylogeny: results from an expanded data set. J. Mol. Evol., 26, 99-121.
-
(1987)
J. Mol. Evol.
, vol.26
, pp. 99-121
-
-
Sibley, C.G.1
Ahlquist, J.E.2
-
30
-
-
0027340263
-
Primate origins: Plugging the gaps
-
Martin, R.D. (1993) Primate origins: plugging the gaps. Nature, 363, 223-234.
-
(1993)
Nature
, vol.363
, pp. 223-234
-
-
Martin, R.D.1
-
32
-
-
0029278906
-
The origin and function of the mammalian Y chromosomes and Y-borne genes - An evolving understanding
-
Graves, J.A.M. (1995) The origin and function of the mammalian Y chromosomes and Y-borne genes - an evolving understanding. Bioessays, 17, 311-321.
-
(1995)
Bioessays
, vol.17
, pp. 311-321
-
-
Graves, J.A.M.1
-
33
-
-
0029678404
-
Rapid evolution of human pseudoautosomal genes and their mouse homologs
-
Ellison, J.W., Li, X., Francke, U. and Shapiro, L.J. (1996) Rapid evolution of human pseudoautosomal genes and their mouse homologs. Mamm. Genome, 7, 25-30.
-
(1996)
Mamm. Genome
, vol.7
, pp. 25-30
-
-
Ellison, J.W.1
Li, X.2
Francke, U.3
Shapiro, L.J.4
-
34
-
-
0031435290
-
Man to mouse - Lessons learned from the distal end of the human X chromosome
-
Blaschke, R.J. and Rappold, G.A. (1997) Man to mouse - lessons learned from the distal end of the human X chromosome. Genome Res., 7, 1114-1117.
-
(1997)
Genome Res.
, vol.7
, pp. 1114-1117
-
-
Blaschke, R.J.1
Rappold, G.A.2
-
35
-
-
0026557719
-
Mammalian phylogeny: Shaking the tree
-
Novacek, M.J. (1992) Mammalian phylogeny: shaking the tree. Nature, 356, 121-125.
-
(1992)
Nature
, vol.356
, pp. 121-125
-
-
Novacek, M.J.1
-
36
-
-
0025651769
-
Evolution of the pseudoautosomal boundary in old world monkeys and great apes
-
Ellis, N., Yen, P., Neiswanger, K., Shapiro, L.J. and Goodfellow, P.N. (1990) Evolution of the pseudoautosomal boundary in old world monkeys and great apes. Cell, 63, 977-986.
-
(1990)
Cell
, vol.63
, pp. 977-986
-
-
Ellis, N.1
Yen, P.2
Neiswanger, K.3
Shapiro, L.J.4
Goodfellow, P.N.5
-
37
-
-
0028343234
-
Cloning of PBDX, a MIC2-related gene that spans the pseudoautosomal boundary on chromosome Xp
-
Ellis, N.A., Ye, T.Z., German, J., Goodfellow, P.N. and Weller, P. (1994) Cloning of PBDX, a MIC2-related gene that spans the pseudoautosomal boundary on chromosome Xp. Nature Genet., 6, 394-400.
-
(1994)
Nature Genet.
, vol.6
, pp. 394-400
-
-
Ellis, N.A.1
Ye, T.Z.2
German, J.3
Goodfellow, P.N.4
Weller, P.5
-
38
-
-
0345437765
-
The human Y chromosome homologue of XG: Transcription of a naturally truncated gene
-
Weller, P.A., Critcher, R., Goodfellow, P.N., German, J. and Ellis, N.A. (1995) The human Y chromosome homologue of XG: transcription of a naturally truncated gene. Hum. Mol. Genet., 1, 587-591.
-
(1995)
Hum. Mol. Genet.
, vol.1
, pp. 587-591
-
-
Weller, P.A.1
Critcher, R.2
Goodfellow, P.N.3
German, J.4
Ellis, N.A.5
-
39
-
-
0023241709
-
Genetic heterogeneity of steroid sulfatase deficiency revealed with cDNA for human steroid sulfatase
-
Conary, J.T., Lorkowski, G., Schmidt, B., Pohlmann, R., Nagel, G., Meyer, H.E., Krentler, C., Cully, J., Hasilik, A. and von Figura, K. (1987) Genetic heterogeneity of steroid sulfatase deficiency revealed with cDNA for human steroid sulfatase. Biochem. Biophys. Res. Commun., 144, 1010-1017.
-
(1987)
Biochem. Biophys. Res. Commun.
, vol.144
, pp. 1010-1017
-
-
Conary, J.T.1
Lorkowski, G.2
Schmidt, B.3
Pohlmann, R.4
Nagel, G.5
Meyer, H.E.6
Krentler, C.7
Cully, J.8
Hasilik, A.9
Von Figura, K.10
-
40
-
-
0026600244
-
Specific metaphase and interphase detection of the breakpoint region in 8q24 of Burkitt lymphoma cells by triple-color fluorescent in situ hybridization
-
Ried, T., Lengauer, C., Cremer, T., Wiegant, J., Raap, A., van der Ploeg, M., Groitl, P. and Lipp, M. (1992) Specific metaphase and interphase detection of the breakpoint region in 8q24 of Burkitt lymphoma cells by triple-color fluorescent in situ hybridization. Genes Chromosomes Cancer, 4, 69-74.
-
(1992)
Genes Chromosomes Cancer
, vol.4
, pp. 69-74
-
-
Ried, T.1
Lengauer, C.2
Cremer, T.3
Wiegant, J.4
Raap, A.5
Van Der Ploeg, M.6
Groitl, P.7
Lipp, M.8
-
41
-
-
0030940217
-
Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and turner syndrome
-
Rao, E., Weiss, B., Fukami, M., Rump, A., Niesler, B., Mertz, A., Muroya, K., Binder, G., Kirsch, S., Winkelmann, M., Nordsiek, G., Heinrich, U., Breuning, M.H., Ranke, M.B., Rosenthal, A., Ogata, T. and Rappold, G.A. (1997) Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome. Nature Genet., 16, 54-63.
-
(1997)
Nature Genet.
, vol.16
, pp. 54-63
-
-
Rao, E.1
Weiss, B.2
Fukami, M.3
Rump, A.4
Niesler, B.5
Mertz, A.6
Muroya, K.7
Binder, G.8
Kirsch, S.9
Winkelmann, M.10
Nordsiek, G.11
Heinrich, U.12
Breuning, M.H.13
Ranke, M.B.14
Rosenthal, A.15
Ogata, T.16
Rappold, G.A.17
-
42
-
-
0027509067
-
A human pseudoautosomal gene, ADP/ATP translocase, escapes X-inactivation whereas a homologue on Xq is subject to X-inactivation
-
Schiebel, K., Weiss, B., Wöhrle, D. and Rappold, G.A. (1993) A human pseudoautosomal gene, ADP/ATP translocase, escapes X-inactivation whereas a homologue on Xq is subject to X-inactivation. Nature Genet., 3, 82-87.
-
(1993)
Nature Genet.
, vol.3
, pp. 82-87
-
-
Schiebel, K.1
Weiss, B.2
Wöhrle, D.3
Rappold, G.A.4
-
43
-
-
0029032452
-
Comparative mapping of YRRM-and TSPY-related cosmids in man and hominoid apes
-
Schempp, W., Binkele, A., Arnemann, J., Gläser, B., Ma, K., Taylor, K., Toder, R., Wolfe, J., Zeitler, S. and Chandley, A.C. (1995) Comparative mapping of YRRM-and TSPY-related cosmids in man and hominoid apes. Chromosome Res., 3, 227-234.
-
(1995)
Chromosome Res.
, vol.3
, pp. 227-234
-
-
Schempp, W.1
Binkele, A.2
Arnemann, J.3
Gläser, B.4
Ma, K.5
Taylor, K.6
Toder, R.7
Wolfe, J.8
Zeitler, S.9
Chandley, A.C.10
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