Consensus Statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies (2010)
- Authors:
- Miller, David T.
- Adam, Margaret P.
- Aradhya, Swaroop
- Biesecker, Leslie G. - National Institutes of Health (NIH)
- Brothman, Arthur R.
- Carter, Nigel P
- Church, Deanna M.
- Crolla, John, A
- Eichler, E.
- Epstein, Charles J
- Faucett, W. Andrew
- Feuk, Lars
- Friedman, Jan M
- Hamosh, Ada
- Jackson, Laird
- Kaminsky, Erin B.
- Kok, Klaas
- Krantz, Ian D. - University of Pennsylvania (UP)
- Kuhn, Robert H
- Lee, Charles
- Ostell, James M.
- Rosenberg, Carla

- Scherer, Stephen W
- Spinner, Nancy B. - University of Pennsylvania (UP)
- Stavropoulos, Dimitri J.
- Tepperberg, James H.
- Thorland, Erik C.
- Vermeesch, Joris R
- Waggoner, Darrel J. - University of Chicago (UC)
- Watson, Michael S.
- Martin, Christa Lese
- Ledbetter, David H.
- Autor USP: ROSENBERG, CARLA - IB
- Unidade: IB
- DOI: 10.1016/j.ajhg.2010.04.006
- Subjects: DOENÇAS GENÉTICAS; DIAGNÓSTICO CLÍNICO
- Language: Inglês
- Imprenta:
- Source:
- Título: The American Journal of Human Genetics
- ISSN: 0002-9297
- Volume/Número/Paginação/Ano: v. 86 n. 5, p. 749-764, may 2010
- Status:
- Artigo possui acesso gratuito no site do editor (Bronze Open Access)
- Versão do Documento:
- Versão publicada (Published version)
- Acessar versão aberta:
-
ABNT
MILLER, David T. et al. Consensus Statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. The American Journal of Human Genetics, v. 86 n. 5, p. 749-764, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.ajhg.2010.04.006. Acesso em: 12 maio 2026. -
APA
Miller, D. T., Adam, M. P., Aradhya, S., Biesecker, L. G., Brothman, A. R., Carter, N. P., et al. (2010). Consensus Statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. The American Journal of Human Genetics, 86 n. 5, 749-764. doi:10.1016/j.ajhg.2010.04.006 -
NLM
Miller DT, Adam MP, Aradhya S, Biesecker LG, Brothman AR, Carter NP, Church DM, Crolla J, Eichler E, Epstein CJ, Faucett WA, Feuk L, Friedman JM, Hamosh A, Jackson L, Kaminsky EB, Kok K, Krantz ID, Kuhn RH, Lee C, Ostell JM, Rosenberg C, Scherer SW, Spinner NB, Stavropoulos DJ, Tepperberg JH, Thorland EC, Vermeesch JR, Waggoner DJ, Watson MS, Martin CL, Ledbetter DH. Consensus Statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies [Internet]. The American Journal of Human Genetics. 2010 ; 86 n. 5 749-764.[citado 2026 maio 12 ] Available from: https://doi.org/10.1016/j.ajhg.2010.04.006 -
Vancouver
Miller DT, Adam MP, Aradhya S, Biesecker LG, Brothman AR, Carter NP, Church DM, Crolla J, Eichler E, Epstein CJ, Faucett WA, Feuk L, Friedman JM, Hamosh A, Jackson L, Kaminsky EB, Kok K, Krantz ID, Kuhn RH, Lee C, Ostell JM, Rosenberg C, Scherer SW, Spinner NB, Stavropoulos DJ, Tepperberg JH, Thorland EC, Vermeesch JR, Waggoner DJ, Watson MS, Martin CL, Ledbetter DH. Consensus Statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies [Internet]. The American Journal of Human Genetics. 2010 ; 86 n. 5 749-764.[citado 2026 maio 12 ] Available from: https://doi.org/10.1016/j.ajhg.2010.04.006 - Array-CGH analysis in patients with Goldenhar Syndrome
- Dosage Changes of a Segment at 17p13.1 Lead to Intellectual Disability and Microcephaly as a Result of Complex Genetic Interaction of Multiple Genes
- Germline BAX deletion in a patient with melanoma and gastrointestinal stromal tumor. [Carta para o editor]
- TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia
- Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridization
- Desvendado mecanismo de mutação genética ligada à deficiência intelectual. [Depoimento]
- High frequency of submicroscopic chromosomal deletions and duplications in dysmorphic patients born small for gestational age
- Number of rare germline CNVs and TP53 mutation types
- A familial case with interstitial 2q36 deletion: variable phenotypic expression in full and mosaic state
- Li-Fraumeni-like syndrome associated with a large BRCA1 intragenic deletion
Informações sobre a disponibilidade de versões do artigo em acesso aberto coletadas automaticamente via oaDOI API (Unpaywall).
Por se tratar de integração com serviço externo, podem existir diferentes versões do trabalho (como preprints ou postprints), que podem diferir da versão publicada.
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
