Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia
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S. Mundlos | F. Westermann | N. Laing | M. Cunningham | P. Nürnberg | S. Tinschert | C. Mischung | H. Thiele | K. Uhlmann | H. Ritter | W. Höhne | D. Chandler | G. Leschik | K. Harrop | J. Goldblatt | Z. Borochowitz | D. Kotzot | H. Braun | Heide Ritter
[1] M. Passos-Bueno,et al. Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia. , 2000, American journal of medical genetics.
[2] D. Kingsley,et al. Role of the mouse ank gene in control of tissue calcification and arthritis. , 2000, Science.
[3] S. Tinschert,et al. Craniometaphyseal dysplasia in six generations of a German kindred. , 1998, American journal of medical genetics.
[4] J. Hampe,et al. The gene for autosomal dominant craniometaphyseal dysplasia maps to chromosome 5p and is distinct from the growth hormone-receptor gene. , 1997, American journal of human genetics.
[5] E. Schönau,et al. Autosomal-dominante kraniometaphysäre Dysplasie , 1996, Monatsschrift Kinderheilkunde.
[6] Cécile Fizames,et al. A comprehensive genetic map of the human genome based on 5,264 microsatellites , 1996, Nature.
[7] M. Doherty,et al. Localisation of a gene for chondrocalcinosis to chromosome 5p. , 1995, Human molecular genetics.
[8] P. Beighton. Craniometaphyseal dysplasia (CMD), autosomal dominant form. , 1995, Journal of medical genetics.
[9] J. Thompson,et al. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. , 1994, Nucleic acids research.
[10] J. Wasmuth,et al. Molecular and phenotypic mapping of the short arm of chromosome 5: sublocalization of the critical region for the cri-du-chat syndrome. , 1994, Human molecular genetics.
[11] D. B. Taylor,et al. Dominant craniometaphyseal dysplasia--a family study over five generations. , 1989, Australasian radiology.
[12] David Eisenberg,et al. The helical hydrophobic moment: a measure of the amphiphilicity of a helix , 1982, Nature.
[13] F. Albright,et al. Metaphyseal dysplasia, epiphyseal dysplasia, diaphyseal dysplasia, and related conditions. III. Progressive diaphyseal dysplasia. , 1954, A.M.A. archives of internal medicine.
[14] M. Devoto,et al. Refinement of the chromosome 5p locus for familial calcium pyrophosphate dihydrate deposition disease. , 1999, American journal of human genetics.
[15] Kay Hofmann,et al. Tmbase-A database of membrane spanning protein segments , 1993 .
[16] H. Fleisch. Diphosphonates: history and mechanisms of action. , 1981, Metabolic bone disease & related research.