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Volumn 45, Issue 1, 2015, Pages 4-9

Prenatal exome sequencing for fetuses with structural abnormalities: The next step

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME ABERRATION; EXOME; FEMALE; GENETIC COUNSELING; HUMAN; NUCLEOTIDE SEQUENCE; PILOT STUDY; PREGNANCY; PRENATAL DIAGNOSIS; PROGNOSIS; TRENDS;

EID: 84920878583     PISSN: 09607692     EISSN: 14690705     Source Type: Journal    
DOI: 10.1002/uog.14653     Document Type: Editorial
Times cited : (57)

References (27)
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    • (2014) J Child Neurol
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  • 9
    • 2942575149 scopus 로고    scopus 로고
    • A cytogeneticist's perspective on genomic microarrays
    • Shaffer LG, Bejjani BA. A cytogeneticist's perspective on genomic microarrays. Hum Reprod Update 2004; 10: 221-226.
    • (2004) Hum Reprod Update , vol.10 , pp. 221-226
    • Shaffer, L.G.1    Bejjani, B.A.2
  • 11
    • 0033048717 scopus 로고    scopus 로고
    • A case of recurrent congenital fetal anomalies associated with a familial subtelomeric translocation
    • Brackley KJ, Kilby MD, Morton J, Whittle MJ, Knight SJ, Flint J. A case of recurrent congenital fetal anomalies associated with a familial subtelomeric translocation. Prenat Diagn 1999; 19: 570-574.
    • (1999) Prenat Diagn , vol.19 , pp. 570-574
    • Brackley, K.J.1    Kilby, M.D.2    Morton, J.3    Whittle, M.J.4    Knight, S.J.5    Flint, J.6
  • 14
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    • The Human Gene Mutation Database: Providing a comprehensive central mutation database for molecular diagnostics and personalized genomics
    • Stenson PD, Ball EV, Howells K, Phillips AD, Mort M, Cooper DN. The Human Gene Mutation Database: providing a comprehensive central mutation database for molecular diagnostics and personalized genomics. Hum Genomics 2009; 4: 69-72.
    • (2009) Hum Genomics , vol.4 , pp. 69-72
    • Stenson, P.D.1    Ball, E.V.2    Howells, K.3    Phillips, A.D.4    Mort, M.5    Cooper, D.N.6
  • 16
    • 84891855440 scopus 로고    scopus 로고
    • The role and challenges of exome sequencing in studies of human diseases
    • Wang Z, Liu X, Yang BZ, Gelernter J. The role and challenges of exome sequencing in studies of human diseases. Front Genet 2013; 4: 160.
    • (2013) Front Genet , vol.4 , pp. 160
    • Wang, Z.1    Liu, X.2    Yang, B.Z.3    Gelernter, J.4
  • 18
    • 77953936166 scopus 로고    scopus 로고
    • The human phenotype ontology
    • Robinson PN, Mundlos S. The human phenotype ontology. Clin Genet 2010; 77: 525-534.
    • (2010) Clin Genet , vol.77 , pp. 525-534
    • Robinson, P.N.1    Mundlos, S.2
  • 21
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    • Cardiac malformation in two infants with hypochondrogenesis
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.