High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers

[1]  A. Michael,et al.  Gene mapping in Alport families with different basement membrane antigenic phenotypes. , 1990, Kidney international.

[2]  M. Skolnick,et al.  Identification of mutations in the COL4A5 collagen gene in Alport syndrome. , 1990, Science.

[3]  D. Sheer,et al.  Molecular cloning of alpha 5(IV) collagen and assignment of the gene to the region of the X chromosome containing the Alport syndrome locus. , 1990, American journal of human genetics.

[4]  S P Kwan,et al.  Identification of a closely linked DNA marker, DXS178, to further refine the X-linked agammaglobulinemia locus. , 1990, Genomics.

[5]  R. Eddy,et al.  Identification of a distinct type IV collagen alpha chain with restricted kidney distribution and assignment of its gene to the locus of X chromosome-linked Alport syndrome. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[6]  A. Michael,et al.  Identification of variant Alport phenotypes using an Alport-specific antibody probe. , 1989, Kidney international.

[7]  M. Bobrow,et al.  Localization of the gene for classic Alport syndrome. , 1989, Genomics.

[8]  C. Julier,et al.  Linkage studies in X-linked Alport's syndrome , 1988, Human Genetics.

[9]  H. Brunner,et al.  Localization of the gene for X-linked Alport's syndrome. , 1988, Kidney international.

[10]  Y. Nakamura,et al.  Isolation and mapping of a polymorphic DNA sequence (pYNH3) on chromosome X [DXS287]. , 1988, Nucleic acids research.

[11]  M. Skolnick,et al.  Mapping of Alport syndrome to the long arm of the X chromosome. , 1988, American journal of human genetics.

[12]  P. Szabo,et al.  An anonymous single copy X-chromosome clone DXS94 from Xq11-q21 identifies a common RFLP. , 1987, Nucleic acids research.

[13]  A. Clarke,et al.  X-linked hypohidrotic ectodermal dysplasia: DNA probe linkage analysis and gene localization , 1987, Human Genetics.

[14]  E. Lander,et al.  Construction of multilocus genetic linkage maps in humans. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[15]  K. Kidd,et al.  MSP RFLP for X-linked proteolipid protein gene (PLP) identified with either rat or human PLP cDNA clone. , 1987, Nucleic acids research.

[16]  M. Wapenaar,et al.  The X chromosome shows less genetic variation at restriction sites than the autosomes. , 1986, American journal of human genetics.

[17]  C. Atkin,et al.  Genetic heterogeneity among kindreds with Alport syndrome. , 1986, American journal of human genetics.

[18]  L. Tsui,et al.  Cystic Fibrosis Locus Defined by a Genetically Linked Polymorphic Dna Marker Author(s): Lap , 2022 .

[19]  J. Ott,et al.  Multilocus linkage analysis in humans: detection of linkage and estimation of recombination. , 1985, American journal of human genetics.

[20]  T. Holm,et al.  A locus on chromosome 11p with multiple restriction site polymorphisms. , 1984, American journal of human genetics.

[21]  J. Aldridge,et al.  A strategy to reveal high-frequency RFLPs along the human X chromosome. , 1984, American journal of human genetics.

[22]  K. Davies,et al.  Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[23]  C. Atkin,et al.  Early pathologic features of hereditary nephritis: a clinicopathologic correlation. , 1980, Pathology, research and practice.

[24]  C. Atkin,et al.  Hereditary nephritis: a re-examination of its clinical and genetic features. , 1978, Annals of internal medicine.

[25]  K. Grzeschik,et al.  Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome , 2004, Human Genetics.

[26]  M. Gregory,et al.  Single base mutation in alpha 5(IV) collagen chain gene converting a conserved cysteine to serine in Alport syndrome. , 1991, Genomics.

[27]  L. Chow,et al.  Characterization of the 3' half of the human type IV collagen alpha 5 gene that is affected in the Alport syndrome. , 1991, Genomics.

[28]  H. Willard,et al.  Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markers. , 1990, Cytogenetics and cell genetics.

[29]  J. Frézal,et al.  Report of the committee on clinical disorders and chromosomal deletion syndromes. , 1990, Cytogenetics and cell genetics.

[30]  R. Nussbaum,et al.  Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromes. , 1989, Genomics.

[31]  M. Ferguson-Smith,et al.  Report of the committee on clinical disorders and chromosomal deletion syndromes. , 1988, Cytogenetics and cell genetics.

[32]  H. Cooke,et al.  PREPARATION OF X-CHROMOSOME SPECIFIC PROBES FROM A FLOW SORTED LIBRARY , 1985 .