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Volumn 72, Issue 6, 2003, Pages 1578-1584

Definition of a critical region on chromosome 18 for congenital aural atresia by arrayCGH

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BIRTH; CHROMOSOME 18; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL AURAL ATRESIA; EXTERNAL AUDITORY CANAL; EXTERNAL EAR MALFORMATION; GENE AMPLIFICATION; GENE DELETION; GENE MAPPING; GENOME; HUMAN; KARYOTYPING; PRIORITY JOURNAL;

EID: 0037677609     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/375695     Document Type: Article
Times cited : (88)

References (24)
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    • (1988) Adv Otorhinolaryngol , vol.40 , pp. 9-14
    • Cremers, C.W.R.J.1    Teunissen, E.2    Marres, E.H.M.A.3
  • 3
    • 0001441096 scopus 로고
    • Délétion partielle des bras longs du chromosome 18
    • de Grouchy J, Royer P, Salmon CH, Lamy M (1964) Délétion partielle des bras longs du chromosome 18. Pathol Biol 12:579-582
    • (1964) Pathol Biol , vol.12 , pp. 579-582
    • De Grouchy, J.1    Royer, P.2    Salmon, C.H.3    Lamy, M.4
  • 5
    • 0344564142 scopus 로고    scopus 로고
    • Cloning and characterization of ZNF236, a glucose-regulated Kruppel-like zinc-finger gene mapping to human chromosome 18q22-q23
    • Holmes DI, Wahab NA, Mason RM (1999) Cloning and characterization of ZNF236, a glucose-regulated Kruppel-like zinc-finger gene mapping to human chromosome 18q22-q23. Genomics 60:105-109
    • (1999) Genomics , vol.60 , pp. 105-109
    • Holmes, D.I.1    Wahab, N.A.2    Mason, R.M.3
  • 14
    • 0036898231 scopus 로고    scopus 로고
    • Characterizing the physical genome
    • Pollack JR, Iyer VR (2002) Characterizing the physical genome. Nat Genet 32:S515-S521
    • (2002) Nat Genet , vol.32
    • Pollack, J.R.1    Iyer, V.R.2
  • 16
    • 0025827836 scopus 로고
    • Interstitial deletion of the long arm of chromosome 18, del(18) (q12.2q21.1): A report of three cases of an autosomal deletion with a mild phenotype
    • Schinzel A, Binkert F, Lillington DM, Sands M, Stocks RJ, Lindenbaum RH, Matthews H, Sheridan H (1991) Interstitial deletion of the long arm of chromosome 18, del(18) (q12.2q21.1): a report of three cases of an autosomal deletion with a mild phenotype. J Med Genet 28:352-355
    • (1991) J Med Genet , vol.28 , pp. 352-355
    • Schinzel, A.1    Binkert, F.2    Lillington, D.M.3    Sands, M.4    Stocks, R.J.5    Lindenbaum, R.H.6    Matthews, H.7    Sheridan, H.8
  • 20
    • 0026736251 scopus 로고
    • Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer
    • Telenius H, Carter NP, Bebb CE, Nordenskjold M, Ponder BA, Tunnacliffe A (1992) Degenerate oligonucleotide-primed PCR: general amplification of target DNA by a single degenerate primer. Genomics 13:718-725
    • (1992) Genomics , vol.13 , pp. 718-725
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  • 24
    • 0018630218 scopus 로고
    • Syndromes associated with deletion of the long arm of chromosome 18 [del(18q)]
    • Wilson MG, Towner JW, Forsman I, Siris E (1979) Syndromes associated with deletion of the long arm of chromosome 18 [del(18q)]. Am J Med Genet 3:155-174
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.