-
1
-
-
0028942620
-
A 6 Mb YAC contig in Xp22.1-p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, and PHKA2 genes
-
Alitalo T, Francis F, Kere J, Lehrach H, Schlessinger D, Willard HF (1995) A 6 Mb YAC contig in Xp22.1-p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, and PHKA2 genes. Genomics 25:691-700
-
(1995)
Genomics
, vol.25
, pp. 691-700
-
-
Alitalo, T.1
Francis, F.2
Kere, J.3
Lehrach, H.4
Schlessinger, D.5
Willard, H.F.6
-
2
-
-
0025369509
-
A 3.5 genome equivalent multi access YAC library: Construction, characterisation, screening and storage
-
Anand R, Riley JH, Butler R, Smith JC, Markham AF (1990) A 3.5 genome equivalent multi access YAC library: construction, characterisation, screening and storage. Nucleic Acids Res 18: 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
-
3
-
-
0027141519
-
Number of CpG islands and genes in human and mouse
-
Antequera F, Bird A (1993) Number of CpG islands and genes in human and mouse. Proc Natl Acad Sci U.S.A. 90:11995-11999
-
(1993)
Proc Natl Acad Sci U.S.A.
, vol.90
, pp. 11995-11999
-
-
Antequera, F.1
Bird, A.2
-
4
-
-
0028068827
-
Construction of a high-resolution linkage map for Xp22. 1-p22.2 and refinement of the genetic localisation of the Coffin-Lowry syndrome gene
-
Biancalana V, Trivier E, Weber C, Weissenbach J, Rowe PSN, O'Riordan JLH, Partington MW, Heyberger S, Oudet C, Hanauer A (1994) Construction of a high-resolution linkage map for Xp22. 1-p22.2 and refinement of the genetic localisation of the Coffin-Lowry syndrome gene. Genomics 22:617-625
-
(1994)
Genomics
, vol.22
, pp. 617-625
-
-
Biancalana, V.1
Trivier, E.2
Weber, C.3
Weissenbach, J.4
Rowe, P.S.N.5
O'Riordan, J.L.H.6
Partington, M.W.7
Heyberger, S.8
Oudet, C.9
Hanauer, A.10
-
5
-
-
0022540321
-
CpG-rich islands and the function of DNA methylation
-
Bird AP (1986) CpG-rich islands and the function of DNA methylation. Nature 321:209-213
-
(1986)
Nature
, vol.321
, pp. 209-213
-
-
Bird, A.P.1
-
6
-
-
0023472826
-
CpG-rich islands as gene markers in the vertebrate nucleus
-
Bird AP (1987) CpG-rich islands as gene markers in the vertebrate nucleus. Trends Genet 3:342-347
-
(1987)
Trends Genet
, vol.3
, pp. 342-347
-
-
Bird, A.P.1
-
7
-
-
0028804624
-
Cloning of a human insulin-stimulated protein kinase-1 (ISPK-1) gene and analysis of coding regions and mRNA levels of the ISPK-1 gene and the protein phosphatase-1 genes in muscles from NIDDM patients
-
Bjorbaek C, Vik TA, Echwald SM, Yang PY, Vestergaard H, Wang JP, Webb GC, Richmond K, Hansen T, Enkson RL, Gabor-Miklos GL, Cohen PT, Pedeson O (1995) Cloning of a human insulin-stimulated protein kinase-1 (ISPK-1) gene and analysis of coding regions and mRNA levels of the ISPK-1 gene and the protein phosphatase-1 genes in muscles from NIDDM patients. Diabetes 44:90-97
-
(1995)
Diabetes
, vol.44
, pp. 90-97
-
-
Bjorbaek, C.1
Vik, T.A.2
Echwald, S.M.3
Yang, P.Y.4
Vestergaard, H.5
Wang, J.P.6
Webb, G.C.7
Richmond, K.8
Hansen, T.9
Enkson, R.L.10
Gabor-Miklos, G.L.11
Cohen, P.T.12
Pedeson, O.13
-
8
-
-
0024615398
-
X chromosome localisation of the functional gene of the El alpha subunit of the human pyruvate dehydrogenase complex
-
Brown RM, Dahl H-HM, Brown GK (1989) X chromosome localisation of the functional gene of the El alpha subunit of the human pyruvate dehydrogenase complex. Genomics 4:174-181
-
(1989)
Genomics
, vol.4
, pp. 174-181
-
-
Brown, R.M.1
Dahl, H.-H.M.2
Brown, G.K.3
-
9
-
-
0026878925
-
Dinucleotide polymorphisms at the DXS365, DXS443 and DXS451 loci
-
Browne D, Barker D, Litt M (1992) Dinucleotide polymorphisms at the DXS365, DXS443 and DXS451 loci. Hum Mol Genet 1:213
-
(1992)
Hum Mol Genet
, vol.1
, pp. 213
-
-
Browne, D.1
Barker, D.2
Litt, M.3
-
10
-
-
0026607209
-
Walking, cloning and mapping with yeast artificial chromosomes: Contig encompassing D21S13 and D21S16
-
Butler R, Ogilvie DJ, Elvin P, Riley JH, Finniear RS, Slynn G, Morten JEN, Markham AF, Anand R (1992) Walking, cloning and mapping with yeast artificial chromosomes: contig encompassing D21S13 and D21S16. Genomics 12:42-51
-
(1992)
Genomics
, vol.12
, pp. 42-51
-
-
Butler, R.1
Ogilvie, D.J.2
Elvin, P.3
Riley, J.H.4
Finniear, R.S.5
Slynn, G.6
Morten, J.E.N.7
Markham, A.F.8
Anand, R.9
-
11
-
-
0141520905
-
An electrophoretic karyotype for yeast
-
Carle GF, Olson MV (1985) An electrophoretic karyotype for yeast. Proc Natl Acad Sci USA 82:3756-3760
-
(1985)
Proc Natl Acad Sci USA
, vol.82
, pp. 3756-3760
-
-
Carle, G.F.1
Olson, M.V.2
-
12
-
-
0027723477
-
A first generation physical map of the human genome
-
Cohen D, Chumakov I, Weissenbach J (1993) A first generation physical map of the human genome. Nature 366:698-701
-
(1993)
Nature
, vol.366
, pp. 698-701
-
-
Cohen, D.1
Chumakov, I.2
Weissenbach, J.3
-
13
-
-
0026849567
-
Positional cloning: Let's not call it reverse any more
-
Collins FS (1992) Positional cloning: let's not call it reverse any more. Nature genet 1:3-6
-
(1992)
Nature Genet
, vol.1
, pp. 3-6
-
-
Collins, F.S.1
-
14
-
-
13344285144
-
Fine mapping of keratosis spinulosa decalvans (KFSD) in Xp22
-
Den Dunnen JT, Van Der Wielen MJR, Voorhoeve E, Bakker E. Van Ommen GJB, Oosterwijk JC (1994) Fine mapping of keratosis spinulosa decalvans (KFSD) in Xp22. Cytogenet Cell Genet 67:336, S24
-
(1994)
Cytogenet Cell Genet
, vol.67
, pp. 336
-
-
Den Dunnen, J.T.1
Van Der Wielen, M.J.R.2
Voorhoeve, E.3
Bakker, E.4
Van Ommen, G.J.B.5
Oosterwijk, J.C.6
-
15
-
-
0027949070
-
Fine structure mapping of the human X-linked hypophosphataemic rickets gene locus
-
Econs MJ, Rowe PSN, Francis F, Barker DF, Speer MC, Norman M, Fain PR. Weissenbach J, Read A, Davies KE, Becker PA, Lehrach H, O'Riordan J. Drezner MK (1994) Fine structure mapping of the human X-linked hypophosphataemic rickets gene locus. J Clin Endocrinol Metab 79:1351-1354
-
(1994)
J Clin Endocrinol Metab
, vol.79
, pp. 1351-1354
-
-
Econs, M.J.1
Rowe, P.S.N.2
Francis, F.3
Barker, D.F.4
Speer, M.C.5
Norman, M.6
Fain, P.R.7
Weissenbach, J.8
Read, A.9
Davies, K.E.10
Becker, P.A.11
Lehrach, H.12
O'Riordan, J.13
Drezner, M.K.14
-
16
-
-
0020793569
-
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
-
Feinberg AP, Vogelstein B (1983) A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal Biochem 132:6-13
-
(1983)
Anal Biochem
, vol.132
, pp. 6-13
-
-
Feinberg, A.P.1
Vogelstein, B.2
-
17
-
-
0028361036
-
A YAC contig spanning the hypophosphataemic rickets disease gene (HYP) candidate region
-
Francis F, Rowe PSN, Econs MJ, Gee See C, Benham F, O'Riordan JLH, Drezner MK, Hamvas RMJ, Lehrach H (1993) A YAC contig spanning the hypophosphataemic rickets disease gene (HYP) candidate region. Genomics 21:229-237
-
(1993)
Genomics
, vol.21
, pp. 229-237
-
-
Francis, F.1
Rowe, P.S.N.2
Econs, M.J.3
Gee See, C.4
Benham, F.5
O'Riordan, J.L.H.6
Drezner, M.K.7
Hamvas, R.M.J.8
Lehrach, H.9
-
18
-
-
0028231090
-
The 1993-1994 Genethon human genetic linkage map
-
Gyapay G, Morissette J, Vignal A, Dib C, Fizames C, Millasseau P, Marc S, Bemardi G, Lathrop M, Weissenbach J (1994) The 1993-1994 Genethon human genetic linkage map. Nature Genet 7:246-339
-
(1994)
Nature Genet
, vol.7
, pp. 246-339
-
-
Gyapay, G.1
Morissette, J.2
Vignal, A.3
Dib, C.4
Fizames, C.5
Millasseau, P.6
Marc, S.7
Bemardi, G.8
Lathrop, M.9
Weissenbach, J.10
-
19
-
-
18744437089
-
Localisation of a new type of X-linked liver glycogenosis to the chromosomal region Xp22 containing the liver alpha-subunit of phosphorylase kinase (PHKA2)
-
Hendrickx J, Coucke P, Hors-Cayla M-C. Smit GPA, Shin YS, Deutsch J, Smeitink J, Berger R, Lee P, Fernandes J, Willems PJ (1994) Localisation of a new type of X-linked liver glycogenosis to the chromosomal region Xp22 containing the liver alpha-subunit of phosphorylase kinase (PHKA2). Genomics 21:620-625
-
(1994)
Genomics
, vol.21
, pp. 620-625
-
-
Hendrickx, J.1
Coucke, P.2
Hors-Cayla, M.-C.3
Smit, G.P.A.4
Shin, Y.S.5
Deutsch, J.6
Smeitink, J.7
Berger, R.8
Lee, P.9
Fernandes, J.10
Willems, P.J.11
-
20
-
-
0011187199
-
Mapping of the Xp22 region surrounding the gene responsible for spondyloepiphyseal dysplasia
-
Heuertz E, Smahi A, Hors-Cayla MC (1994) Mapping of the Xp22 region surrounding the gene responsible for spondyloepiphyseal dysplasia. Cytogenet Cell Genet 67:340, S38
-
(1994)
Cytogenet Cell Genet
, vol.67
, pp. 340
-
-
Heuertz, E.1
Smahi, A.2
Hors-Cayla, M.C.3
-
21
-
-
0025163052
-
Second generation approach to the construction of yeast artificial-chromosome libraries
-
Imai T, Olson MV (1990) Second generation approach to the construction of yeast artificial-chromosome libraries. Genomics 8: 297-303
-
(1990)
Genomics
, vol.8
, pp. 297-303
-
-
Imai, T.1
Olson, M.V.2
-
22
-
-
0021816507
-
Mapping DNA sequences in a human X chromosome deletion which exlends across the region of the Duchenne muscular dystrophy mutation
-
Ingle C, Williamson R, Chapelle A de la, Herva RR, Haapala K. Bates G, Willard HF, Pearson P. Davies KE (1985) Mapping DNA sequences in a human X chromosome deletion which exlends across the region of the Duchenne muscular dystrophy mutation. Am J Hum Genet 37:451-462
-
(1985)
Am J Hum Genet
, vol.37
, pp. 451-462
-
-
Ingle, C.1
Williamson, R.2
De La Chapelle, A.3
Herva, R.R.4
Haapala, K.5
Bates, G.6
Willard, H.F.7
Pearson, P.8
Davies, K.E.9
-
23
-
-
0026440240
-
Mapping human chromosomes by walking with sequence-tagged sites from end fragments of yeast artificial chromosome inserts
-
Kere J, Nagaraja R, Mumm S, Ciccodicolo A, D'Urso M. Sclessinger D (1992). Mapping human chromosomes by walking with sequence-tagged sites from end fragments of yeast artificial chromosome inserts. Genomics 14:241-248
-
(1992)
Genomics
, vol.14
, pp. 241-248
-
-
Kere, J.1
Nagaraja, R.2
Mumm, S.3
Ciccodicolo, A.4
D'Urso, M.5
Sclessinger, D.6
-
24
-
-
0027939214
-
The role of recombination and RAD52 in mutations of chromosomal DNA transformed into yeast
-
Larionov V, Graves J, Kouprina N, Resnick MA (1994a) The role of recombination and RAD52 in mutations of chromosomal DNA transformed into yeast. Nucleic Acids Res 22:4234-4241
-
(1994)
Nucleic Acids Res
, vol.22
, pp. 4234-4241
-
-
Larionov, V.1
Graves, J.2
Kouprina, N.3
Resnick, M.A.4
-
25
-
-
0028004127
-
Recombination during transformation as a source of chimeric mammalian artificial chromosomes in yeast (YACs)
-
Larionov V, Kouprina N, Nikolaishvili N, Resnick MA (1994b) Recombination during transformation as a source of chimeric mammalian artificial chromosomes in yeast (YACs). Nucleic Acids Res 22:4154-4162
-
(1994)
Nucleic Acids Res
, vol.22
, pp. 4154-4162
-
-
Larionov, V.1
Kouprina, N.2
Nikolaishvili, N.3
Resnick, M.A.4
-
26
-
-
0026553755
-
Construction and characterisation of a YAC library for Xpter-Xq27.3: A systematic determination of the cocloning rate and X chromosome representation
-
Lee JT, Murgai A, Sosnoski DM, Olivos IM, Nussbaum RL (1992) Construction and characterisation of a YAC library for Xpter-Xq27.3: a systematic determination of the cocloning rate and X chromosome representation. Genomics 12:526-533
-
(1992)
Genomics
, vol.12
, pp. 526-533
-
-
Lee, J.T.1
Murgai, A.2
Sosnoski, D.M.3
Olivos, I.M.4
Nussbaum, R.L.5
-
27
-
-
0019272411
-
Expression of an X-linked gene from an inactive human X-chromosome in mouse-human hybrid cells: Further evidence for the non-inactivation of the steroid sulphatase locus in man
-
Mohandas T, Sparkes RS, Hellkuhl K, Grzeschik KH, Shapiro LJ (1980) Expression of an X-linked gene from an inactive human X-chromosome in mouse-human hybrid cells: further evidence for the non-inactivation of the steroid sulphatase locus in man. Proc Natl Acad Sci USA 77:6759-6763
-
(1980)
Proc Natl Acad Sci USA
, vol.77
, pp. 6759-6763
-
-
Mohandas, T.1
Sparkes, R.S.2
Hellkuhl, K.3
Grzeschik, K.H.4
Shapiro, L.J.5
-
28
-
-
0028114080
-
Characterisation of four human YAC libraries for clone size, chimerism, and X chromosome sequence representation
-
Nagaraja R, Kere J, MacMillan S, Masisi MWJ, Johnson D, Molini BJ, Halley GR, Wein K, Trusnich M, Eble B, Railey B, Brownstein BH, Schlessinger D (1994) Characterisation of four human YAC libraries for clone size, chimerism, and X chromosome sequence representation. Nucleic Acids Res 22: 3406-3411
-
(1994)
Nucleic Acids Res
, vol.22
, pp. 3406-3411
-
-
Nagaraja, R.1
Kere, J.2
MacMillan, S.3
Mwj, M.4
Johnson, D.5
Molini, B.J.6
Halley, G.R.7
Wein, K.8
Trusnich, M.9
Eble, B.10
Railey, B.11
Brownstein, B.H.12
Schlessinger, D.13
-
30
-
-
0026865130
-
A donor splice site mutation in the parathyroid hormone gene is associated with autosomal recessive hypoparathyroidism
-
Parkinson DB, Thakker RV (1992) A donor splice site mutation in the parathyroid hormone gene is associated with autosomal recessive hypoparathyroidism. Nature Genet 1:149-152
-
(1992)
Nature Genet
, vol.1
, pp. 149-152
-
-
Parkinson, D.B.1
Thakker, R.V.2
-
31
-
-
0023749255
-
X-linked mental retardation with dystonic movements of the hands
-
Partington MW, Mulley JC, Sutherland GR, Hockey A, Thode A, Turner G (1988) X-linked mental retardation with dystonic movements of the hands. Am J Med Genet 30:251-262
-
(1988)
Am J Med Genet
, vol.30
, pp. 251-262
-
-
Partington, M.W.1
Mulley, J.C.2
Sutherland, G.R.3
Hockey, A.4
Thode, A.5
Turner, G.6
-
32
-
-
0022730336
-
Molecular and physical arrangements of human DNA in HRASI-selected chromosome-mediated transfectants
-
Porteous DJ, Morten JEN, Cranston G, Fletcher JM, Mitchell A, Van Heyningen V, Fantes JA, Boyd PA, Hastie ND (1986) Molecular and physical arrangements of human DNA in HRASI-selected chromosome-mediated transfectants. Mol Cell Biol 6: 2223-2232
-
(1986)
Mol Cell Biol
, vol.6
, pp. 2223-2232
-
-
Porteous, D.J.1
Morten, J.E.N.2
Cranston, G.3
Fletcher, J.M.4
Mitchell, A.5
Van Heyningen, V.6
Fantes, J.A.7
Boyd, P.A.8
Hastie, N.D.9
-
33
-
-
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 JC, Markham AF (1990) A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones. Nucleic Acids Res 18:2887-2890
-
(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
-
34
-
-
0027219492
-
New markers for linkage analysis of X linked hypophosphataemic rickets
-
Rowe PSN, Gouldins J, Read A, Mountford R, Hanauer A, Oudet C. Whyte MP, Meier Ewert S, Lehrach H, Davies KE. O'Riordan JLH (1993) New markers for linkage analysis of X linked hypophosphataemic rickets. Hum Genet 91:571-575
-
(1993)
Hum Genet
, vol.91
, pp. 571-575
-
-
Psn, R.1
Gouldins, J.2
Read, A.3
Mountford, R.4
Hanauer, A.5
Oudet, C.6
Whyte, M.P.7
Meier Ewert, S.8
Lehrach, H.9
Davies, K.E.10
O'Riordan, J.L.H.11
-
35
-
-
0028091087
-
Refining the genetic map for the region flanking the X-linked hypophosphataemic rickets locus (Xp22.1-22.2)
-
Rowe PSN, Goulding J, Read A, Lehrach H, Francis F, Hanauer A, Oudet C, Biancalana V, Kooh SW, Davies KE, O'Riordan JLH (1994) Refining the genetic map for the region flanking the X-linked hypophosphataemic rickets locus (Xp22.1-22.2). Hum Genet 93:291-294
-
(1994)
Hum Genet
, vol.93
, pp. 291-294
-
-
Rowe, P.S.N.1
Goulding, J.2
Read, A.3
Lehrach, H.4
Francis, F.5
Hanauer, A.6
Oudet, C.7
Biancalana, V.8
Kooh, S.W.9
Davies, K.E.10
O'Riordan, J.L.H.11
-
36
-
-
0027177179
-
Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies
-
Scheinman SJ, Pook MA, Wooding C, Pang JT, Frymoyer PA. Thakker RV (1993) Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies. J Clin Invest 91:2351-2357
-
(1993)
J Clin Invest
, vol.91
, pp. 2351-2357
-
-
Scheinman, S.J.1
Pook, M.A.2
Wooding, C.3
Pang, J.T.4
Frymoyer, P.A.5
Thakker, R.V.6
-
37
-
-
0002062060
-
Pulsed-field gel electrophoresis and the technology of large DNA molecules
-
Davies KE (ed) IRL, Oxford
-
Smith CL, Klco SR, Cantor CR (1988) Pulsed-field gel electrophoresis and the technology of large DNA molecules. In: Davies KE (ed) Genome analysis: a practical approach. IRL, Oxford, pp 41-72
-
(1988)
Genome Analysis: A Practical Approach
, pp. 41-72
-
-
Smith, C.L.1
Klco, S.R.2
Cantor, C.R.3
-
38
-
-
0016700864
-
Detection of specific sequences among DNA fragments separated by gel electrophoresis
-
Southern EM (1975) Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol 98: 503-517
-
(1975)
J Mol Biol
, vol.98
, pp. 503-517
-
-
Southern, E.M.1
-
39
-
-
0025173321
-
Linkage analysis of two cloned DNA sequences, DXS197 and DXS207. in hypophosphataemic rickets families
-
Thakker RV, Davies KE, Read AP, Tippett P, Wooding C, Flint T, Wood S, Kruse TA, Whyte MP, O'Riordan JLH (1990) Linkage analysis of two cloned DNA sequences, DXS197 and DXS207. in hypophosphataemic rickets families. Genomics 8: 189-193
-
(1990)
Genomics
, vol.8
, pp. 189-193
-
-
Thakker, R.V.1
Davies, K.E.2
Read, A.P.3
Tippett, P.4
Wooding, C.5
Flint, T.6
Wood, S.7
Kruse, T.A.8
Whyte, M.P.9
O'Riordan, J.L.H.10
-
40
-
-
13344285863
-
Construction of a YAC contig in the human Xp22.1 region
-
Van Den Vosse E, Meerchoek EJ, Van Ommen GJB, Den Dunnen JT (1994) Construction of a YAC contig in the human Xp22.1 region. Cytogenet Cell Genet 67:336, S25
-
(1994)
Cytogenet Cell Genet
, vol.67
, pp. 336
-
-
Van Den Vosse, E.1
Meerchoek, E.J.2
Van Ommen, G.J.B.3
Den Dunnen, J.T.4
-
41
-
-
0021354895
-
Towards a complete linkage map of the human X chromosome: Regional assignment of 17 cloned single copy DNA sequences employing a panel of somatic cell hybrids
-
Wieacker P, Davies KE, Cooke HJ, Pearson PL, Williamson R, Bhattacharya S, Zimmer J, Ropers HH (1984) Towards a complete linkage map of the human X chromosome: regional assignment of 17 cloned single copy DNA sequences employing a panel of somatic cell hybrids. Am J Hum Genet 36:265-276
-
(1984)
Am J Hum Genet
, vol.36
, pp. 265-276
-
-
Wieacker, P.1
Davies, K.E.2
Cooke, H.J.3
Pearson, P.L.4
Williamson, R.5
Bhattacharya, S.6
Zimmer, J.7
Ropers, H.H.8
-
42
-
-
0027936475
-
Report of the 5th International Workshop on Human X Chromosome Mapping 1994
-
Willard HF, Cremers F, Mandel JL, Monaco AP, Nelson DL, Schlessinger D (1994) Report of the 5th International Workshop on Human X Chromosome Mapping 1994. Cytogenet Cell Genet 67:295-358
-
(1994)
Cytogenet Cell Genet
, vol.67
, pp. 295-358
-
-
Willard, H.F.1
Cremers, F.2
Mandel, J.L.3
Monaco, A.P.4
Nelson, D.L.5
Schlessinger, D.6
-
43
-
-
0025974894
-
Mapping of the gene for X-linked liver glycogenosis due to phophorylase kinase deficiency to human chromosome region Xp22
-
Willems PJ, Hendrickx J, Van Der Auwera BJ, Vits L, Raeymackers P, Coucke PJ, Van Der Bergh I, Berger R, Smit GPA, Van Broeckhoven C, Kilimann MW, Van Elson AF, Fernandes JF (1991) Mapping of the gene for X-linked liver glycogenosis due to phophorylase kinase deficiency to human chromosome region Xp22. Genomics 9:565-569
-
(1991)
Genomics
, vol.9
, pp. 565-569
-
-
Willems, P.J.1
Hendrickx, J.2
Van Der Auwera, B.J.3
Vits, L.4
Raeymackers, P.5
Coucke, P.J.6
Van Der Bergh, I.7
Berger, R.8
Smit, G.P.A.9
Van Broeckhoven, C.10
Kilimann, M.W.11
Van Elson, A.F.12
Fernandes, J.F.13
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