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Volumn 29, Issue 9, 2009, Pages 884-888

Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array-CGH

Author keywords

Array CGH; Congenital diaphragmatic hernia; Deletion 15q; Prenatal diagnosis; Ring chromosome 15

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHILD; CHORION VILLUS SAMPLING; CHROMOSOME 15; CHROMOSOME ABERRATION; COMPARATIVE GENOMIC HYBRIDIZATION; DNA DETERMINATION; DNA SEQUENCE; DOWN SYNDROME; FEMALE; FETUS; FETUS ECHOGRAPHY; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN TISSUE; MONOSOMY; MOSAICISM; NUCHAL TRANSLUCENCY MEASUREMENT; POLYACRYLAMIDE GEL ELECTROPHORESIS; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; PRESCHOOL CHILD; PRIORITY JOURNAL; RING CHROMOSOME;

EID: 69749125262     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.2295     Document Type: Article
Times cited : (8)

References (11)
  • 1
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  • 5
    • 34347225551 scopus 로고    scopus 로고
    • Molecular characterization of a ring chromosome 15 in a fetus with intra uterine growth retardation and diaphragmatic hernia
    • DOI 10.1002/pd.1707
    • Hatem E, Meriam BR, Walid D, Adenen M, Moez G, Ali S. 2007. Molecular characterization of a ring chromosome 15 in a fetus with intra uterine growth retardation and diaphragmatic hernia. Prenat Diagn 27: 471-474. (Pubitemid 47164348)
    • (2007) Prenatal Diagnosis , vol.27 , Issue.5 , pp. 471-474
    • Hatem, E.1    Meriam, B.R.2    Walid, D.3    Adenen, M.4    Moez, G.5    Ali, S.6
  • 7
    • 0023153582 scopus 로고
    • Does 'ring syndrome' exist? An analysis of 207 case reports on patients with a ring autosome
    • DOI 10.1007/BF00591082
    • Kosztolanyi G. 1987. Does "ring syndrome" exist? An analysis of 207 case reports on patients with a ring autosome. Hum Genet 75: 174-179. (Pubitemid 17017714)
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    • Kosztolanyi, G.1
  • 8
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    • Increased fetal nuchal fold leading to prenatal diagnosis of ring chromosome 15
    • Liu YH, Chang SD, Chen FP. 2001. Increased fetal nuchal fold leading to prenatal diagnosis of ring chromosome 15. Prenat Diagn 21: 1031-1033.
    • (2001) Prenat Diagn , vol.21 , pp. 1031-1033
    • Liu, Y.H.1    Chang, S.D.2    Chen, F.P.3
  • 9
    • 0141532992 scopus 로고    scopus 로고
    • A girl with cutaneous hyperpigmentation, cafe au lait spots and ring chromosome 15 without significant deletion
    • Morava E, Bartsch O, Czako M, Frensel A, Karteszi J, Kosztolanyi GY. 2003. A girl with cutaneous hyperpigmentation, cafe au lait spots and ring chromosome 15 without significant deletion. Genet Couns 14: 337-342. (Pubitemid 37210412)
    • (2003) Genetic Counseling , vol.14 , Issue.3 , pp. 337-342
    • Morava, E.1    Bartsch, O.2    Czako, M.3    Frensel, A.4    Karteszi, J.5    Kosztolanyt, G.Y.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.