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9 results for Karyotyping+-+standards

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Gale Encyclopedia of Science.
Publisher:FARMINGTON HILLS : Cengage Gale, 2021.
Edition:6th ed.
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Subtelomeric aberrations in Thai patients with idiopathic mental retardation and autism detected by multiplex ligation-dependent probe amplification
Author / Creator:Rujirabanjerd, Sinitdhorn ; Plong-on, Oradawan ; Sripo, Thanya ; Limprasert, Pornprot
Publisher:Bangkok: De Gruyter Poland
Journal title:Asian biomedicine, 2015-01, Vol.9 (4), p.501-509
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In-house genetic counseling increases the detection of abnormal karyotypes—a 26-year experience in prenatal diagnosis in a single tertiary referral hospital in Poland
Author / Creator:Bijok, Julia ; Kucińska–Chahwan, Anna ; Massalska, Diana ; Ilnicka, Alicja ; Panek, Grzegorz ; Roszkowski, Tomasz
Publisher:New York: Springer US
Journal title:Journal of assisted reproduction and genetics, 2020-08, Vol.37 (8), p.1999-2006
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Replacing the Combined Test by Cell-Free DNA Testing in Screening for Trisomies 21, 18 and 13: Impact on the Diagnosis of Other Chromosomal Abnormalities
Author / Creator:Syngelaki, Argyro ; Pergament, Eugene ; Homfray, Tessa ; Akolekar, Ranjit ; Nicolaides, Kypros H.
Publisher:Basel, Switzerland: S. Karger AG
Journal title:Fetal diagnosis and therapy, 2014-06, Vol.35 (3), p.174-184
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Efficiency of noninvasive prenatal testing for the detection of fetal microdeletions and microduplications in autosomal chromosomes
Author / Creator:Pei, Yuanyuan ; Hu, Liang ; Liu, Jinxing ; Wen, Lijuan ; Luo, Xiaojin ; Lu, Jian ; Wei, Fengxiang
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2020-08, Vol.8 (8), p.e1339-n/a
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Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotype
Author / Creator:Su, Linjuan ; Huang, Hailong ; An, Gang ; Cai, Meiying ; Wu, Xiaoqing ; Li, Ying ; Xie, Xiaorui ; Lin, Yuan ; Wang, Meiying ; Xu, Liangpu
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2019-08, Vol.7 (8), p.e811-n/a
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Rescue karyotyping: a case series of array-based comparative genomic hybridization evaluation of archival conceptual tissue
Author / Creator:Kudesia, Rashmi ; Li, Marilyn ; Smith, Janice ; Patel, Ankita ; Williams, Zev
Publisher:England: BioMed Central Ltd
Journal title:Reproductive biology and endocrinology, 2014-03, Vol.12 (1), p.19-19, Article 19
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A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21
Author / Creator:Li, Jin ; Xie, Mingshui ; Wang, Fang ; Ma, Jianhong ; Li, Jiafu ; Chen, Chen ; Li, Zhimin ; Wang, Juan ; Zhang, Yuanzhen ; Li, Yirong
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2020-08, Vol.8 (8), p.e1279-n/a
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Clinical validity of karyotyping for the diagnosis of chromosomal imbalance following array comparative genomic hybridisation
Author / Creator:Gekas, Jean ; Vallée, Maud ; Castonguay, Lysanne ; Laframboise, Rachel ; Maranda, Bruno ; Piedboeuf, Bruno ; Rousseau, François
Publisher:London: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2011-12, Vol.48 (12), p.851-855
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Gale Encyclopedia of Science.

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Subtelomeric aberrations in Thai patients with idiopathic mental retardation and autism detected by multiplex ligation-dependent probe amplification

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In-house genetic counseling increases the detection of abnormal karyotypes—a 26-year experience in prenatal diagnosis in a single tertiary referral hospital in Poland

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Replacing the Combined Test by Cell-Free DNA Testing in Screening for Trisomies 21, 18 and 13: Impact on the Diagnosis of Other Chromosomal Abnormalities

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Efficiency of noninvasive prenatal testing for the detection of fetal microdeletions and microduplications in autosomal chromosomes

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Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotype

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Rescue karyotyping: a case series of array-based comparative genomic hybridization evaluation of archival conceptual tissue

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A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21

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Clinical validity of karyotyping for the diagnosis of chromosomal imbalance following array comparative genomic hybridisation

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