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Volumn 101, Issue 2, 2003, Pages 103-105

Supernumerary small marker chromosome (SMC) and uniparental disomy 22 in a child with confined placental mosaicism of trisomy 22: Trisomy rescue due to marker chromosome formation

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 14; CHROMOSOME 22; CHROMOSOME SATELLITE ASSOCIATION; CONGENITAL HEART MALFORMATION; DIGESTIVE SYSTEM MALFORMATION; ECHOGRAPHY; EXTRACHROMOSOMAL INHERITANCE; FEMALE; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; FOLLOW UP; HUMAN; MARKER CHROMOSOME; MATERNAL AGE; MEIOSIS; MENTAL DEVELOPMENT; MOLECULAR PROBE; MOTOR DEVELOPMENT; NEWBORN; PHENOTYPE; PLACENTA; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SEX CHROMOSOME MOSAICISM; SUPERNUMERARY CHROMOSOME; TRISOMY; TRISOMY 22; UNIPARENTAL DISOMY; ZYGOTE;

EID: 0345448878     PISSN: 14248581     EISSN: None     Source Type: Journal    
DOI: 10.1159/000074163     Document Type: Article
Times cited : (29)

References (7)
  • 1
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    • A second case of intrauterine growth retardation and primary hypospadias associated with a trisomy 22 placenta but with biparental inheritance of chromosome 22 in the fetus
    • Bryan J, Peters M, Pritchard G, Healey S, Payton D: A second case of intrauterine growth retardation and primary hypospadias associated with a trisomy 22 placenta but with biparental inheritance of chromosome 22 in the fetus. Prenat Diag 22:137-40 (2002).
    • (2002) Prenat Diag , vol.22 , pp. 137-140
    • Bryan, J.1    Peters, M.2    Pritchard, G.3    Healey, S.4    Payton, D.5
  • 2
    • 0023840501 scopus 로고
    • An embryonic model to explain cytogenetic inconsistencies observed in chorionic versus fetal tissues
    • Crane JP, Cheung SW: An embryonic model to explain cytogenetic inconsistencies observed in chorionic versus fetal tissues. Prenat Diag 8:119-129 (1988).
    • (1988) Prenat Diag , vol.8 , pp. 119-129
    • Crane, J.P.1    Cheung, S.W.2
  • 3
    • 0042320679 scopus 로고    scopus 로고
    • A series of supernumerary small ring marker autosomes identified by FISH with chromosome probe arrays and literature review excluding chromosome 15
    • Daniel A, Malafiej P: A series of supernumerary small ring marker autosomes identified by FISH with chromosome probe arrays and literature review excluding chromosome 15. Am J med Genet 117A:212-222 (2003).
    • (2003) Am J Med Genet , vol.117 A , pp. 212-222
    • Daniel, A.1    Malafiej, P.2
  • 4
    • 0036796014 scopus 로고    scopus 로고
    • Supernumerary marker chromosomes (SMC) and uniparental disomy (UPD): Coincidence or consequence?
    • Kotzot D: Supernumerary marker chromosomes (SMC) and uniparental disomy (UPD): coincidence or consequence? J med Genet 39:775-778 (2002).
    • (2002) J Med Genet , vol.39 , pp. 775-778
    • Kotzot, D.1
  • 6
    • 7344254106 scopus 로고    scopus 로고
    • A catalogue of imprinted genes and parent-of-origin effects in humans and animals
    • Morison IM, Reeve AE: A catalogue of imprinted genes and parent-of-origin effects in humans and animals. Hum molec Genet 7:1599-1609 (1998).
    • (1998) Hum Molec Genet , vol.7 , pp. 1599-1609
    • Morison, I.M.1    Reeve, A.E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.