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Volumn 22, Issue 4, 2013, Pages 172-174

An infant with trisomy 15 mosaicism

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BRAIN MALFORMATION; CASE REPORT; CESAREAN SECTION; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CLINICAL FEATURE; DISEASE SEVERITY; ECHOCARDIOGRAPHY; ECHOGRAPHY; EPICANTHUS; FEMALE; FOREHEAD; HEAD CIRCUMFERENCE; HUMAN; INFANT; KARYOTYPE 46,XX; LABORATORY TEST; MICROGNATHIA; MOSAICISM; MUSCLE TONE; NEUROIMAGING; NEUROLOGIC EXAMINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PALPEBRAL FISSURE; PES EQUINOVARUS; PHYSICAL EXAMINATION; PRIORITY JOURNAL; TENDON REFLEX; THYROID FUNCTION TEST; TRIGONOCEPHALY; TRISOMY; TRISOMY 15;

EID: 84888243273     PISSN: 09628827     EISSN: 14735717     Source Type: Journal    
DOI: 10.1097/MCD.0000000000000012     Document Type: Article
Times cited : (8)

References (11)
  • 1
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  • 4
    • 0025961506 scopus 로고
    • Trisomy 15 associated with nonimmune hydrops
    • Kuller JA, Laifer SA (1991). Trisomy 15 associated with nonimmune hydrops. Am J Perinatol 8:39-40.
    • (1991) Am J Perinatol , vol.8 , pp. 39-40
    • Kuller, J.A.1    Laifer, S.A.2
  • 5
    • 0026638252 scopus 로고
    • Mosaic trisomy found at amniocentesis
    • Lahdetie J, Lakkala T (1992). Mosaic trisomy found at amniocentesis. Prenat Diagn 12:551-552.
    • (1992) Prenat Diagn , vol.12 , pp. 551-552
    • Lahdetie, J.1    Lakkala, T.2
  • 7
    • 0034640677 scopus 로고    scopus 로고
    • Third Prader-Willi syndrome phenotype due to maternal uniparental disomy 15 with trisomy 15
    • Olander E, Stamnerg J, Steinberg L, Wulfsberg EA (2000). Third Prader-Willi syndrome phenotype due to maternal uniparental disomy 15 with trisomy 15. Am J Med Genet 93:215-218.
    • (2000) Am J Med Genet , vol.93 , pp. 215-218
    • Olander, E.1    Stamnerg, J.2    Steinberg, L.3    Wulfsberg, E.A.4
  • 8
    • 33745632137 scopus 로고    scopus 로고
    • Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): Implication for prenatal diagnosis
    • Prontera P, Buldini B, Aiello V, Gruppioni R, Bonfatti A, Venti G, Ferlini A, et al. (2006). Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): implication for prenatal diagnosis. Prenat Diagn 26:571-576.
    • (2006) Prenat Diagn , vol.26 , pp. 571-576
    • Prontera, P.1    Buldini, B.2    Aiello, V.3    Gruppioni, R.4    Bonfatti, A.5    Venti, G.6    Ferlini, A.7
  • 9
    • 0002722022 scopus 로고
    • Trisomy 15 in a mosaic, doubly aneuploid two year old
    • Stallard R, Sommer A (1989). Trisomy 15 in a mosaic, doubly aneuploid two year old. Am J Hum Genet 45 (Suppl):A92.
    • (1989) Am J Hum Genet , vol.45 , Issue.SUPPL.
    • Stallard, R.1    Sommer, A.2
  • 10
    • 0027937004 scopus 로고
    • Nondisjunction of human acrocentric chromosomes: Studies of 432 trisomic fetuses and liveborns
    • Zaragoza MV, Jacobs PA, James RS, Rogan P, Sherman S, Hassold T (1994). Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and liveborns. Hum Genet 94:411-417.
    • (1994) Hum Genet , vol.94 , pp. 411-417
    • Zaragoza, M.V.1    Jacobs, P.A.2    James, R.S.3    Rogan, P.4    Sherman, S.5    Hassold, T.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.