메뉴 건너뛰기




Volumn 31, Issue 1, 1996, Pages 71-79

Narrowing the genetic interval and yeast artificial chromosome map in the branchio-oto-renal region on chromosome 8q

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

EID: 0030026159     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0011     Document Type: Article
Times cited : (12)

References (40)
  • 1
    • 0025368589 scopus 로고
    • Construction and characterization of a yeast artificial chromosome library containing seven haploid genome equivalents
    • Albertsen, O. H., Abderrahim, H., Cann, H. M., Dausset, J., Le Paslier, D., and Cohen, D. (1990). Construction and characterization of a yeast artificial chromosome library containing seven haploid genome equivalents. Proc. Natl. Acad. Sci. USA 87: 4256-4260.
    • (1990) Proc. Natl. Acad. Sci. USA , vol.87 , pp. 4256-4260
    • Albertsen, O.H.1    Abderrahim, H.2    Cann, H.M.3    Dausset, J.4    Le Paslier, D.5    Cohen, D.6
  • 2
    • 0015406970 scopus 로고
    • Deafness and familial congenital auricular fistulas
    • Bailleul, J. P., Libersa, C., and Laude, M. (1972). Deafness and familial congenital auricular fistulas. Pediatrie 27: 739-747.
    • (1972) Pediatrie , vol.27 , pp. 739-747
    • Bailleul, J.P.1    Libersa, C.2    Laude, M.3
  • 3
    • 0027723477 scopus 로고
    • A first-generation physical map of the human genome
    • Cohen, D., Chumakov, I., and 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
  • 7
    • 0000914168 scopus 로고
    • Hereditary deafness in a family with ear-pits (fistula auris congenital)
    • Fourman, P., and Fourman, J. (1955). Hereditary deafness in a family with ear-pits (fistula auris congenital). Br. Med. J. 2: 1354-1356.
    • (1955) Br. Med. J. , vol.2 , pp. 1354-1356
    • Fourman, P.1    Fourman, J.2
  • 8
    • 0018254276 scopus 로고
    • Genetic aspects of the BOR syndrome-branchial fistulas, ear pits, hearing loss, and renal anomalies
    • Fraser, F. C., Ling, D., Clogg, D., and Nogrady, B. (1978). Genetic aspects of the BOR syndrome-branchial fistulas, ear pits, hearing loss, and renal anomalies. Am. J. Med. Genet. 2: 241-252.
    • (1978) Am. J. Med. Genet. , vol.2 , pp. 241-252
    • Fraser, F.C.1    Ling, D.2    Clogg, D.3    Nogrady, B.4
  • 9
    • 0019165942 scopus 로고
    • Frequency of the branchio-oto-renal (BOR) syndrome in children with profound hearing loss
    • Fraser, F. C., Sproule, J. R., and Halal, F. (1980). Frequency of the branchio-oto-renal (BOR) syndrome in children with profound hearing loss. Am. J. Med. Genet. 7: 341-349.
    • (1980) Am. J. Med. Genet. , vol.7 , pp. 341-349
    • Fraser, F.C.1    Sproule, J.R.2    Halal, F.3
  • 11
    • 0024403636 scopus 로고
    • Tricho-rhino-phalangeal and branchio-oto-renal syndrome in a family with an inherited rearrangement of chromosome 8q
    • Haan, E. A., Hull, Y. J., White, S., Cockington, P., Charlton, P., and Callen, D. F. (1989). Tricho-rhino-phalangeal and branchio-oto-renal syndrome in a family with an inherited rearrangement of chromosome 8q. Am. J. Med. Genet. 32: 490-494.
    • (1989) Am. J. Med. Genet. , vol.32 , pp. 490-494
    • Haan, E.A.1    Hull, Y.J.2    White, S.3    Cockington, P.4    Charlton, P.5    Callen, D.F.6
  • 12
    • 0022461894 scopus 로고
    • Branchio-oto-renal syndrome: Reduced penetrance and variable expressivity in four generations of a large kindred
    • Heimler, A., and Lieber, E. (1986). Branchio-oto-renal syndrome: Reduced penetrance and variable expressivity in four generations of a large kindred. Am. J. Med. Genet. 25: 15-27.
    • (1986) Am. J. Med. Genet. , vol.25 , pp. 15-27
    • Heimler, A.1    Lieber, E.2
  • 13
    • 34447583132 scopus 로고
    • Hals-Kieman-Fisteln von noch nicht beobachteter form
    • Heusinger, C. F. (1864). Hals-Kieman-Fisteln von noch nicht beobachteter Form. Virchows Arch. Pathol. Anat. Physiol. 29: 358-380.
    • (1864) Virchows Arch. Pathol. Anat. Physiol. , vol.29 , pp. 358-380
    • Heusinger, C.F.1
  • 14
    • 0015979531 scopus 로고
    • Inheritance of branchial sinuses and preauricular fistulae
    • Hunter, A. G. W. (1974). Inheritance of branchial sinuses and preauricular fistulae. Teratology 9: 225-228.
    • (1974) Teratology , vol.9 , pp. 225-228
    • Hunter, A.G.W.1
  • 15
    • 0026941761 scopus 로고
    • Autosomal dominant branchio-oto-renal syndrome - Localization of a disease gene to chromosome 8q by linkage in a Dutch family
    • Kumar, S., Kimberling, W. J., Kenyon, J. B., Smith, R. J. H., Marres, H. A. M., and Cremers, C. W. R. J. (1992). Autosomal dominant branchio-oto-renal syndrome - Localization of a disease gene to chromosome 8q by linkage in a Dutch family. Human Mol. Genet. 7: 491-495.
    • (1992) Human Mol. Genet. , vol.7 , pp. 491-495
    • Kumar, S.1    Kimberling, W.J.2    Kenyon, J.B.3    Smith, R.J.H.4    Marres, H.A.M.5    Cremers, C.W.R.J.6
  • 16
    • 0028062167 scopus 로고
    • Refining the region of branchio-oto-renal syndrome and defining the flanking markers on chromosome 8q by genetic mapping
    • Kumar, S., Kimberling, W. J., Connoly, C. J., Tinley, S., Marres, H. A. M., and Cremers, C. W. R. J. (1994). Refining the region of branchio-oto-renal syndrome and defining the flanking markers on chromosome 8q by genetic mapping. Am. J. Hum. Genet. 55: 1188-1194.
    • (1994) Am. J. Hum. Genet. , vol.55 , pp. 1188-1194
    • Kumar, S.1    Kimberling, W.J.2    Connoly, C.J.3    Tinley, S.4    Marres, H.A.M.5    Cremers, C.W.R.J.6
  • 17
    • 0021850103 scopus 로고
    • Multilocus linkage analysis in humans: Detection of linkage and estimation of recombination
    • Lathrop, G. M., Lalouel, J. M., Julier, C., and Ott, J. (1985). Multilocus linkage analysis in humans: Detection of linkage and estimation of recombination. Am. J. Hum. Genet. 37: 482-498.
    • (1985) Am. J. Hum. Genet. , vol.37 , pp. 482-498
    • Lathrop, G.M.1    Lalouel, J.M.2    Julier, C.3    Ott, J.4
  • 18
    • 84965344209 scopus 로고
    • Lateral cervical and preauricular sinuses: Their transmission as dominant characters
    • Martins, A. G. (1961). Lateral cervical and preauricular sinuses: Their transmission as dominant characters. Br. Med. J. 1: 255-256.
    • (1961) Br. Med. J. , vol.1 , pp. 255-256
    • Martins, A.G.1
  • 20
    • 0343292052 scopus 로고
    • Hereditary branchial anomalies and associated hearing impairment
    • McLaurin, J. W., Kloepfer, H. W., Laguaite, J. K., and Stallcup, T. A. (1966). Hereditary branchial anomalies and associated hearing impairment. Laryngoscope 76: 1277-1288.
    • (1966) Laryngoscope , vol.76 , pp. 1277-1288
    • McLaurin, J.W.1    Kloepfer, H.W.2    Laguaite, J.K.3    Stallcup, T.A.4
  • 21
    • 0016880752 scopus 로고
    • Familial branchio-oto-renal dysplasia: A new addition to the branchial arch syndromes
    • Melnick, M., Bixler, D., Nance, W. E., Silk, K., and Yune, H. (1976). Familial branchio-oto-renal dysplasia: A new addition to the branchial arch syndromes. Clin. Genet. 9: 25-34.
    • (1976) Clin. Genet. , vol.9 , pp. 25-34
    • Melnick, M.1    Bixler, D.2    Nance, W.E.3    Silk, K.4    Yune, H.5
  • 24
    • 0026774858 scopus 로고
    • A comprehensive genetic linkage map of the human genome
    • NIH/CEPH collaborative mapping group (1992). A comprehensive genetic linkage map of the human genome. Science 258: 67-86.
    • (1992) Science , vol.258 , pp. 67-86
  • 26
    • 0026589638 scopus 로고
    • Shoulder abnormalities in association with branchio-oto-renal dysplasia in a patient who also has familial joint laxity
    • Pennie, B. H., and Marres, H. A. M. (1992). Shoulder abnormalities in association with branchio-oto-renal dysplasia in a patient who also has familial joint laxity. Int. J. Pediat. Otorhinolaryngol. 23: 269-273.
    • (1992) Int. J. Pediat. Otorhinolaryngol. , vol.23 , pp. 269-273
    • Pennie, B.H.1    Marres, H.A.M.2
  • 28
    • 0014631799 scopus 로고
    • Familial hearing loss associated with branchial fistulas
    • Rowley, P. T. (1969). Familial hearing loss associated with branchial fistulas. Pediatrics 44: 978-985.
    • (1969) Pediatrics , vol.44 , pp. 978-985
    • Rowley, P.T.1
  • 30
    • 0023504973 scopus 로고
    • Purification, specific fragmentation, and separation of large DNA molecules
    • Smith, C. L., and Cantor, C. R. (1987). Purification, specific fragmentation, and separation of large DNA molecules. Methods Enzymol. 155: 449-467.
    • (1987) Methods Enzymol. , vol.155 , pp. 449-467
    • Smith, C.L.1    Cantor, C.R.2
  • 33
    • 0025744677 scopus 로고
    • Mapping of the MYC gene to band 8q24.12 > q24.13 by R-banding and distal to fra(8)(q24.11), FRA8E, by fluorescence in situ hybridization
    • Takashi, E., Hori, T., O'Connel, P. O., Leppert, M., and White, R. (1991). Mapping of the MYC gene to band 8q24.12 > q24.13 by R-banding and distal to fra(8)(q24.11), FRA8E, by fluorescence in situ hybridization. Cytogenet. Cell Genet. 57: 109-111.
    • (1991) Cytogenet. Cell Genet. , vol.57 , pp. 109-111
    • Takashi, E.1    Hori, T.2    O'Connel, P.O.3    Leppert, M.4    White, R.5
  • 35
    • 0026017360 scopus 로고
    • Mapping of human chromosome Xq28 by two color fluorescence in situ hybridization of DNA sequences to interphase cell nuclei
    • Trask, B. J., Massa, H., Kenwrick, S., and Gitschier, J. (1991). Mapping of human chromosome Xq28 by two color fluorescence in situ hybridization of DNA sequences to interphase cell nuclei. Am. J. Hum. Genet. 48: 1-15.
    • (1991) Am. J. Hum. Genet. , vol.48 , pp. 1-15
    • Trask, B.J.1    Massa, H.2    Kenwrick, S.3    Gitschier, J.4
  • 36
    • 0027940062 scopus 로고
    • A proposed new contiguous gene syndrome on 8q consists of branchio-oto-renal (BOR) syndrome. Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR gene
    • Vincent, C., Kalatzis, V., Compain, S., Levilliers, J., Slim, R., Graia, F., Pereira, M. L., Nivelon, A., Croquette, M. F., Lacombe, D., et al. (1994). A proposed new contiguous gene syndrome on 8q consists of branchio-oto-renal (BOR) syndrome. Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR gene. Hum. Mol. Genet. 3: 1859-1866.
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 1859-1866
    • Vincent, C.1    Kalatzis, V.2    Compain, S.3    Levilliers, J.4    Slim, R.5    Graia, F.6    Pereira, M.L.7    Nivelon, A.8    Croquette, M.F.9    Lacombe, D.10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.