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Refinado por: Base de dados/Biblioteca: AUC Wiley Frozen Package in 2012 remover assunto: Karyotyping remover xxx: xxx remover
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1
Coamplification of Myc/Pvt1 and homozygous deletion of Nlrp1 locus are frequent genetics changes in mouse osteosarcoma
Coamplification of Myc/Pvt1 and homozygous deletion of Nlrp1 locus are frequent genetics changes in mouse osteosarcoma
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Coamplification of Myc/Pvt1 and homozygous deletion of Nlrp1 locus are frequent genetics changes in mouse osteosarcoma

Rao, Pulivarthi H. ; Zhao, Shuying ; Zhao, Yi-Jue ; Yu, Alexander ; Rainusso, Nino ; Trucco, Matteo ; Allen-Rhoades, Wendy ; Satterfield, Laura ; Fuja, Daniel ; Borra, Vishnupriya J. ; Man, Tsz-Kwong ; Donehower, Lawrence A. ; Yustein, Jason T.

Genes chromosomes & cancer, 2015-12, Vol.54 (12), p.796-808 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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2
Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray‐based analysis
Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray‐based analysis
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Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray‐based analysis

Mademont‐Soler, I. ; Morales, C. ; Soler, A. ; MartÍnez‐Crespo, J. M. ; Shen, Y. ; Margarit, E. ; Clusellas, N. ; Obón, M. ; Wu, B.‐L. ; Sánchez, A.

Ultrasound in obstetrics & gynecology, 2013-04, Vol.41 (4), p.375-382 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

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3
Two genetic pathways, t(1;10) and amplification of 3p11-12, in myxoinflammatory fibroblastic sarcoma, haemosiderotic fibrolipomatous tumour, and morphologically similar lesions
Two genetic pathways, t(1;10) and amplification of 3p11-12, in myxoinflammatory fibroblastic sarcoma, haemosiderotic fibrolipomatous tumour, and morphologically similar lesions
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Two genetic pathways, t(1;10) and amplification of 3p11-12, in myxoinflammatory fibroblastic sarcoma, haemosiderotic fibrolipomatous tumour, and morphologically similar lesions

Hallor, Karolin H ; Sciot, Raf ; Staaf, Johan ; Heidenblad, Markus ; Rydholm, Anders ; Bauer, Henrik CF ; Åström, Kristina ; Domanski, Henryk A ; Meis, Jeanne M ; Kindblom, Lars-Gunnar ; Panagopoulos, Ioannis ; Mandahl, Nils ; Mertens, Fredrik

The Journal of pathology, 2009-04, Vol.217 (5), p.716-727 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

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4
Rapid aneusomy detection in products of conception using the KaryoLite™ BACs-on-Beads™ assay
Rapid aneusomy detection in products of conception using the KaryoLite™ BACs-on-Beads™ assay
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Rapid aneusomy detection in products of conception using the KaryoLite™ BACs-on-Beads™ assay

Paxton, Christian N. ; Brothman, Arthur R. ; Geiersbach, Katherine B.

Prenatal diagnosis, 2013-01, Vol.33 (1), p.25-31 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

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5
Prevalence of mosaicism in uncultured chorionic villus samples after chromosomal microarray and clinical outcome in pregnancies affected by confined placental mosaicism
Prevalence of mosaicism in uncultured chorionic villus samples after chromosomal microarray and clinical outcome in pregnancies affected by confined placental mosaicism
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Prevalence of mosaicism in uncultured chorionic villus samples after chromosomal microarray and clinical outcome in pregnancies affected by confined placental mosaicism

Lund, Ida C. B. ; Becher, Naja ; Christensen, Rikke ; Petersen, Olav B. ; Steffensen, Ellen H. ; Vestergaard, Else M. ; Vogel, Ida

Prenatal diagnosis, 2020-01, Vol.40 (2), p.244-259 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

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6
Chromosomal abnormalities detected by karyotyping and microarray analysis in twins with structural anomalies
Chromosomal abnormalities detected by karyotyping and microarray analysis in twins with structural anomalies
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Chromosomal abnormalities detected by karyotyping and microarray analysis in twins with structural anomalies

Li, L. ; He, Z. ; Huang, X. ; Lin, S. ; Wu, J. ; Huang, L. ; Wan, Y. ; Fang, Q.

Ultrasound in obstetrics & gynecology, 2020-04, Vol.55 (4), p.502-509 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

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7
International Society for Prenatal Diagnosis Updated Position Statement on the use of genome‐wide sequencing for prenatal diagnosis
International Society for Prenatal Diagnosis Updated Position Statement on the use of genome‐wide sequencing for prenatal diagnosis
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International Society for Prenatal Diagnosis Updated Position Statement on the use of genome‐wide sequencing for prenatal diagnosis

Van den Veyver, Ignatia B. ; Chandler, Natalie ; Wilkins‐Haug, Louise E. ; Wapner, Ronald J. ; Chitty, Lyn S.

Prenatal diagnosis, 2022-05, Vol.42 (6), p.796-803 [Periódico revisado por pares]

England: Wiley Subscription Services, Inc

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8
Chromosomal microarray analysis for pregnancies with or without ultrasound abnormalities in women of advanced maternal age
Chromosomal microarray analysis for pregnancies with or without ultrasound abnormalities in women of advanced maternal age
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Chromosomal microarray analysis for pregnancies with or without ultrasound abnormalities in women of advanced maternal age

Wu, Xiaoqing ; An, Gang ; Xie, Xiaorui ; Su, Linjuan ; Cai, Meiying ; Chen, Xuemei ; Li, Ying ; Lin, Na ; He, Deqin ; Wang, Meiying ; Huang, Hailong ; Xu, Liangpu

Journal of clinical laboratory analysis, 2020-04, Vol.34 (4), p.e23117-n/a [Periódico revisado por pares]

United States: John Wiley & Sons, Inc

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9
Cytogenomic array detects a subset of myelodysplastic syndrome with increased risk that is invisible to conventional karyotype
Cytogenomic array detects a subset of myelodysplastic syndrome with increased risk that is invisible to conventional karyotype
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Cytogenomic array detects a subset of myelodysplastic syndrome with increased risk that is invisible to conventional karyotype

Choi, Sarah M. ; Van Norman, Steven B. ; Bixby, Dale L. ; Shao, Lina

Genes chromosomes & cancer, 2019-11, Vol.58 (11), p.756-774 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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10
Detection of partial deletion and mosaicism using quantitative fluorescent polymerase chain reaction: Case reports and a review of the literature
Detection of partial deletion and mosaicism using quantitative fluorescent polymerase chain reaction: Case reports and a review of the literature
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Detection of partial deletion and mosaicism using quantitative fluorescent polymerase chain reaction: Case reports and a review of the literature

Xu, Chenxia ; Peng, Jianming ; Zhang, Yanfang ; Liang, Shaoxia ; Wang, Degang

Journal of clinical laboratory analysis, 2022-08, Vol.36 (8), p.e24574-n/a [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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