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Volumn 132, Issue 3, 2018, Pages E143-E168

ACOG Technology Assessment in Obstetrics and Gynecology No. 14: Modern Genetics in Obstetrics and Gynecology

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ANEUPLOIDY; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE INHERITANCE; CODOMINANCE; CONSANGUINITY; DIAGNOSTIC TEST; DNA SEQUENCING; EPIGENETICS; EXTRACHROMOSOMAL INHERITANCE; GENE DELETION; GENE DUPLICATION; GENETIC HETEROGENEITY; GENETIC POLYMORPHISM; GENETIC SCREENING; GENETIC VARIABILITY; GENETICS; GENOME ANALYSIS; GENOME IMPRINTING; GYNECOLOGIST; GYNECOLOGY; HEALTH CARE PERSONNEL; HUMAN; MEDICAL PRACTICE; MENDELIAN INHERITANCE; MOLECULAR DIAGNOSIS; MONOGENIC DISORDER; MOSAICISM; MULTIFACTORIAL INHERITANCE; OBSTETRICIAN; OBSTETRICS; PATIENT COUNSELING; PENETRANCE; PHENOTYPIC VARIATION; PRENATAL DIAGNOSIS; PREVALENCE; PRIORITY JOURNAL; TECHNOLOGY; TRINUCLEOTIDE REPEAT; UNIPARENTAL DISOMY; WHOLE EXOME SEQUENCING; WHOLE GENOME SEQUENCING; WOMEN'S HEALTH; X CHROMOSOME LINKAGE; HEREDITY;

EID: 85061879214     PISSN: 00297844     EISSN: 1873233X     Source Type: Journal    
DOI: 10.1097/AOG.0000000000002831     Document Type: Article
Times cited : (9)

References (10)
  • 1
    • 84928209346 scopus 로고    scopus 로고
    • Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
    • Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, et al. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med 2015;17:405–24.
    • (2015) Genet Med , vol.17 , pp. 405-424
    • Richards, S1    Aziz, N2    Bale, S3    Bick, D4    Das, S5    Gastier-Foster, J6
  • 2
    • 85026563797 scopus 로고    scopus 로고
    • Carrier screening for genetic conditions. Committee Opinion No. 691. American College of Obstetricians and Gynecologists
    • Carrier screening for genetic conditions. Committee Opinion No. 691. American College of Obstetricians and Gynecologists. Obstet Gynecol 2017;129:e41–55.
    • (2017) Obstet Gynecol , vol.129 , pp. e41-e55
  • 4
    • 77952530338 scopus 로고    scopus 로고
    • Mitochondrial disorders overview
    • Adam MP, Ardinger HH, Pagon RA, Wallace SE, editors. Seattle (WA): University of Washington, Seattle; Retrieved June 1, 2018
    • Chinnery PF. Mitochondrial disorders overview. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, editors. GeneReviewsÒ [Internet]. Seattle (WA): University of Washington, Seattle; 2014. Available at: https://www.ncbi.nlm. nih.gov/books/NBK1224. Retrieved June 1, 2018.
    • (2014) GeneReviewsÒ [Internet]
    • Chinnery, PF.1
  • 5
    • 0013099836 scopus 로고    scopus 로고
    • Genetic counseling and screening of consanguineous couples and their offspring: recommendations of the National Society of Genetic Counselors
    • Bennett RL, Motulsky AG, Bittles A, Hudgins L, Uhrich S, Doyle DL, et al. Genetic counseling and screening of consanguineous couples and their offspring: recommendations of the National Society of Genetic Counselors. J Genet Couns 2002;11:97–119.
    • (2002) J Genet Couns , vol.11 , pp. 97-119
    • Bennett, RL1    Motulsky, AG2    Bittles, A3    Hudgins, L4    Uhrich, S5    Doyle, DL6
  • 6
    • 84922545374 scopus 로고    scopus 로고
    • Application of next-generation sequencing technology in forensic science
    • Yang Y, Xie B, Yan J. Application of next-generation sequencing technology in forensic science. Genomics Proteomics Bioinformatics 2014;12:190–7.
    • (2014) Genomics Proteomics Bioinformatics , vol.12 , pp. 190-197
    • Yang, Y1    Xie, B2    Yan, J.3
  • 7
    • 84892383122 scopus 로고    scopus 로고
    • Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders
    • Cukier HN, Dueker ND, Slifer SH, Lee JM, Whitehead PL, Lalanne E, et al. Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders. Mol Autism 2014;5:1.
    • (2014) Mol Autism , vol.5 , pp. 1
    • Cukier, HN1    Dueker, ND2    Slifer, SH3    Lee, JM4    Whitehead, PL5    Lalanne, E6
  • 8
    • 84943362406 scopus 로고    scopus 로고
    • Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalities. Centre for Translational Genomics
    • Drury S, Williams H, Trump N, Boustred C, Lench N, Scott RH, et al. Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalities. Centre for Translational Genomics. Prenat Diagn 2015;35:1010–7.
    • (2015) Prenat Diagn , vol.35 , pp. 1010-1017
    • Drury, S1    Williams, H2    Trump, N3    Boustred, C4    Lench, N5    Scott, RH6
  • 9
    • 85122619172 scopus 로고    scopus 로고
    • Bethesda (MD): ACMG; Retrieved June 22, 2018
    • American College of Medical Genetics and Genomics. Points to consider in the clinical application of genomic sequencing. Policy Statement. Bethesda (MD): ACMG; 2012. Available at: https://www.acmg.net/staticcontent/ppg/clinical_application_of_genomic_sequencing.pdf. Retrieved June 22, 2018.
    • (2012) Points to consider in the clinical application of genomic sequencing. Policy Statement
  • 10
    • 84996559058 scopus 로고    scopus 로고
    • Microarrays and next-generation sequencing technology: the use of advanced genetic diagnostic tools in obstetrics and gynecology. Committee Opinion No. 682. American College of Obstetricians and Gynecologists
    • Microarrays and next-generation sequencing technology: the use of advanced genetic diagnostic tools in obstetrics and gynecology. Committee Opinion No. 682. American College of Obstetricians and Gynecologists. Obstet Gynecol 2016;128: e262–8.
    • (2016) Obstet Gynecol , vol.128 , pp. e262-e268


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