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Volumn 8, Issue 5, 2000, Pages 393-395

Microdissection of chromosome 2 - Between-arm intrachromosomal insertion

Author keywords

Agangliosis; Chromosome region (2) (q21q23); Intrachromosomal insertion; Microdissection

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 2; CHROMOSOME INSERTION; DNA PROBE; FEMALE; FETUS MALFORMATION; HUMAN; PRIORITY JOURNAL; SPONTANEOUS ABORTION;

EID: 0034079829     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200421     Document Type: Article
Times cited : (8)

References (8)
  • 1
    • 0026602851 scopus 로고
    • Intrachromosomal insertions: A case report and a review
    • Madan K, Menko FH: Intrachromosomal insertions: a case report and a review. Hum Genet 1992; 89: 1-9.
    • (1992) Hum Genet , vol.89 , pp. 1-9
    • Madan, K.1    Menko, F.H.2
  • 4
    • 0029798465 scopus 로고    scopus 로고
    • Microdissection and DOP-PCR-based reverse chromosome painting as a fast and reliable strategy in the analysis of various structural chromosome abnormalities
    • Müller-Navia J, Nebel A, Oehler D, Theile U, Zabel B, Schleiermacher E: Microdissection and DOP-PCR-based reverse chromosome painting as a fast and reliable strategy in the analysis of various structural chromosome abnormalities. Prenat Diagn 1996; 16: 915-922.
    • (1996) Prenat Diagn , vol.16 , pp. 915-922
    • Müller-Navia, J.1    Nebel, A.2    Oehler, D.3    Theile, U.4    Zabel, B.5    Schleiermacher, E.6
  • 6
    • 0031853185 scopus 로고    scopus 로고
    • Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: Delineation of a new syndrome and identification of a locus at chromosome 2q22-q23
    • Mowat DR, Croaker GDH, Cass DT et al: Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23. J Med Genet 1998; 35: 617-623.
    • (1998) J Med Genet , vol.35 , pp. 617-623
    • Mowat, D.R.1    Croaker, G.D.H.2    Cass, D.T.3
  • 7
    • 0031578782 scopus 로고    scopus 로고
    • Aortic stenosis in hypoplastic right heart syndrome, associated with interstitial deletion of chromosome 2
    • Sharma J, Friedman D, Schiller M, Flynn P, Alonso ML: Aortic stenosis in hypoplastic right heart syndrome, associated with interstitial deletion of chromosome 2. Int J Cardiology 1997; 62: 199-202.
    • (1997) Int J Cardiology , vol.62 , pp. 199-202
    • Sharma, J.1    Friedman, D.2    Schiller, M.3    Flynn, P.4    Alonso, M.L.5
  • 8
    • 0024494910 scopus 로고
    • Congenital diaphragmatic hernia, coarse facies and acral hypoplasia: Fryns syndrome
    • Bamforth JS, Leonard CO, Chodirker BN et al: Congenital diaphragmatic hernia, coarse facies and acral hypoplasia: Fryns syndrome. Am J Med Genet 1989; 32: 93-99.
    • (1989) Am J Med Genet , vol.32 , pp. 93-99
    • Bamforth, J.S.1    Leonard, C.O.2    Chodirker, B.N.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.