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X-linked genetic homologies between mouse and man.
Genomics. 1987 Nov;1(3):213-27
PMID: 3328737
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Report of the committee on the genetic constitution of the X and Y chromosomes.
Cytogenet Cell Genet. 1987;46(1-4):277-315
PMID: 3507278
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Transforming growth factor beta modulates the expression of collagenase and metalloproteinase inhibitor.
EMBO J. 1987 Jul;6(7):1899-904
PMID: 2820711
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Human X chromosome markers and Duchenne muscular dystrophy.
Nucleic Acids Res. 1985 May 24;13(10):3419-26
PMID: 3859837
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Lysyl oxidase deficiency in Ehlers-Danlos syndrome type V.
Connect Tissue Res. 1975;3(1):49-53
PMID: 240645
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Human beta-hexosaminidase alpha chain: coding sequence and homology with the beta chain.
Proc Natl Acad Sci U S A. 1985 Dec;82(23):7830-4
PMID: 2933746
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Duchenne muscular dystrophy involving translocation of the dmd gene next to ribosomal RNA genes.
Science. 1984 Jun 29;224(4656):1447-9
PMID: 6729462
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The genetic linkage map of the human X chromosome.
Science. 1985 Nov 15;230(4727):753-8
PMID: 4059909
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Regional mapping panel for human chromosome 17: application to neurofibromatosis type 1.
Genomics. 1987 Dec;1(4):374-81
PMID: 3130306
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A primary genetic map of the pericentromeric region of the human X chromosome.
Genomics. 1988 May;2(4):294-301
PMID: 2906040
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Alterations in copper and collagen metabolism in the Menkes syndrome and a new subtype of the Ehlers-Danlos syndrome.
Biochemistry. 1983 Dec 20;22(26):6156-63
PMID: 6140952
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Genes for synapsin I, a neuronal phosphoprotein, map to conserved regions of human and murine X chromosomes.
Proc Natl Acad Sci U S A. 1986 Nov;83(22):8679-83
PMID: 3095840
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Multilocus molecular mapping of the mouse X chromosome.
Genomics. 1988 Oct;3(3):187-94
PMID: 2906327
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Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy families.
Hum Genet. 1985;71(2):103-7
PMID: 2995231
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Actively transcribed genes in the raf oncogene group, located on the X chromosome in mouse and human.
Proc Natl Acad Sci U S A. 1986 Jun;83(11):3934-8
PMID: 3520560
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Conservation and reorganization of loci on the mammalian X chromosome: a molecular framework for the identification of homologous subchromosomal regions in man and mouse.
Genomics. 1988 Apr;2(3):220-30
PMID: 2899541
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Sequence of human tissue inhibitor of metalloproteinases and its identity to erythroid-potentiating activity.
Nature. 1985 Nov 7-13;318(6041):66-9
PMID: 3903517
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Menkes syndrome in a girl with X-autosome translocation.
Am J Med Genet. 1987 Feb;26(2):503-10
PMID: 3812600
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A sex-linked defect in the cross-linking of collagen and elastin associated with the mottled locus in mice.
J Exp Med. 1974 Jan 1;139(1):180-92
PMID: 4808708
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MspI RFLP detected with chromosome-walk clone pXUT23-SE3.2L from DXS16 in Xp22.1-22.3.
Nucleic Acids Res. 1987 Nov 25;15(22):9614
PMID: 2446265
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Human ornithine transcarbamylase locus mapped to band Xp21.1 near the Duchenne muscular dystrophy locus.
Science. 1984 Nov 9;226(4675):698-700
PMID: 6494904
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Comparative gene mapping: order of loci on the X chromosome is different in mice and humans.
Proc Natl Acad Sci U S A. 1980 Jun;77(6):3595-9
PMID: 6251472
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Assignment of the gene for myelin proteolipid protein to the X chromosome: implications for X-linked myelin disorders.
Science. 1985 Nov 22;230(4728):940-2
PMID: 3840606
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Report of the Committee on the Genetic Constitution of the X and Y Chromosomes.
Cytogenet Cell Genet. 1985;40(1-4):296-352
PMID: 3864598
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Linkage studies in Menkes' disease. The Xg blood group system and C-banding of the X chromosome.
Ann Hum Genet. 1984 May;48(Pt 2):161-72
PMID: 6742777
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Chromosomal assignment of the gene encoding the human tissue inhibitor of metalloproteinases to Xp11.1-p11.4.
Ann Hum Genet. 1987 Jul;51(Pt 3):189-94
PMID: 3688834
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RFLP detected by an X-linked cDNA encoding erythroid-potentiating activity/tissue inhibitor of metalloproteinase (EPA/TIMP).
Nucleic Acids Res. 1986 Nov 25;14(22):9226
PMID: 2878423
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The William Allan memorial award address: X-chromosome inactivation and the location and expression of X-linked genes.
Am J Hum Genet. 1988 Jan;42(1):8-16
PMID: 3276178
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Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus.
Am J Hum Genet. 1985 Mar;37(2):235-49
PMID: 2984924
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X-linked cutis laxa: defective cross-link formation in collagen due to decreased lysyl oxidase activity.
N Engl J Med. 1980 Jul 10;303(2):61-5
PMID: 6104292
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Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation.
Am J Hum Genet. 1985 May;37(3):451-62
PMID: 2988331
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Localization of the gene encoding human erythroid-potentiating activity to chromosome region Xp11.1----Xp11.4.
Am J Hum Genet. 1986 Jun;38(6):819-26
PMID: 3460333
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Assignment of the TIMP gene to the murine X-chromosome using an inter-species cross.
Nucleic Acids Res. 1987 May 26;15(10):4357
PMID: 3588297
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Evidence that the Menkes locus maps on proximal Xp.
Hum Genet. 1983;65(1):72-3
PMID: 6580259
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Molecular characterization and expression of the gene encoding human erythroid-potentiating activity.
Nature. 1985 Jun 27-Jul 3;315(6022):768-71
PMID: 3839290
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Genomic organization of alpha satellite DNA on human chromosome 7: evidence for two distinct alphoid domains on a single chromosome.
Mol Cell Biol. 1987 Jan;7(1):349-56
PMID: 3561394