60k oligo array (BlueGnome Limited)
90
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BlueGnome Limited
60k oligo array
60k Oligo Array, supplied by BlueGnome Limited, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/oligo+array/60k+oligo+array/pm22052739-81-8-14
Average 90 stars, based on 1 article reviews
60k Oligo Array, supplied by BlueGnome Limited, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/oligo+array/60k+oligo+array/pm22052739-81-8-14
Average 90 stars, based on 1 article reviews
60k oligo array - by Bioz Stars,
2026-10
90/100 stars
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Microarray:Article Title: Should we offer prenatal testing for 17q12 microdeletion syndrome to all cases with prenatally diagnosed echogenic kidneys? Prenatal findings in two families with 17q12 microdeletion syndrome and review of the literature. Article Snippet: Objective The objective of this study is to report the prenatal ultrasound scan findings in four fetuses from two families postnatally diagnosed with 17q12 microdeletion syndrome on microarray CGH and review the literature.. Methods We report two families presenting with prenatally detected hyperechogenic kidneys.. In family 1, the mother had three pregnancies complicated by anhydramnios with bilateral hyperechogenic kidneys, hyperechogenic enlarged cystic kidneys, and bilateral hyperechogenic kidneys with polyhydramnios respectively. Article Title: Poster Abstracts of the ISPD 17th International Conference on Prenatal Diagnosis and Therapy Article Snippet: .. These samples were examined by microarray-based comparative genomic hybridization (aCGH) using a 60 K Article Title: 17q12 microdeletion syndrome: three patients illustrating the phenotypic spectrum. Article Snippet: 17q12 Microdeletion Syndrome: Three Patients Illustrating the Phenotypic Spectrum Abhijit Dixit, Chirag Patel, Rachel Harrison, Joanna Jarvis, Sally Hulton, Nigel Smith, Katherine Yates, Lee Silcock, Dominic J. McMullan, and Mohnish Suri* Department of Clinical Genetics, Nottingham City Hospital, Nottingham, UK West Midlands Regional Genetics Service, Birmingham Women’s Hospital, Birmingham, UK Department of Paediatric Nephrology, Birmingham Children’s Hospital, Birmingham, UK Department of Cytogenetics, Nottingham City Hospital, Nottingham, UK Department of Molecular Cytogenetics, Birmingham Women’s Hospital, Birmingham, UK Article Title: Genomic profiling of plasma cell disorders in a clinical setting: integration of microarray and FISH, after CD138 selection of bone marrow Article Snippet: .. Whole genome microarray was performed using an Hybridization:Article Title: Should we offer prenatal testing for 17q12 microdeletion syndrome to all cases with prenatally diagnosed echogenic kidneys? Prenatal findings in two families with 17q12 microdeletion syndrome and review of the literature. Article Snippet: Objective The objective of this study is to report the prenatal ultrasound scan findings in four fetuses from two families postnatally diagnosed with 17q12 microdeletion syndrome on microarray CGH and review the literature.. Methods We report two families presenting with prenatally detected hyperechogenic kidneys.. In family 1, the mother had three pregnancies complicated by anhydramnios with bilateral hyperechogenic kidneys, hyperechogenic enlarged cystic kidneys, and bilateral hyperechogenic kidneys with polyhydramnios respectively. Article Title: Poster Abstracts of the ISPD 17th International Conference on Prenatal Diagnosis and Therapy Article Snippet: .. These samples were examined by microarray-based comparative genomic hybridization (aCGH) using a 60 K Article Title: 17q12 microdeletion syndrome: three patients illustrating the phenotypic spectrum. Article Snippet: 17q12 Microdeletion Syndrome: Three Patients Illustrating the Phenotypic Spectrum Abhijit Dixit, Chirag Patel, Rachel Harrison, Joanna Jarvis, Sally Hulton, Nigel Smith, Katherine Yates, Lee Silcock, Dominic J. McMullan, and Mohnish Suri* Department of Clinical Genetics, Nottingham City Hospital, Nottingham, UK West Midlands Regional Genetics Service, Birmingham Women’s Hospital, Birmingham, UK Department of Paediatric Nephrology, Birmingham Children’s Hospital, Birmingham, UK Department of Cytogenetics, Nottingham City Hospital, Nottingham, UK Department of Molecular Cytogenetics, Birmingham Women’s Hospital, Birmingham, UK other:Article Title: Reassessment of the 12q15 deletion syndrome critical region. Article Snippet: Interstitial deletions of the long arm of chromosome 12 are rare and only few cases have been reported in literature so far, with different phenotypic features related to size and gene content of deleted regions.. Five patients reported a 12q15-q21 deletion, sharing a 1.3 Mb small region of overlap (SRO) and presenting with developmental delay, nasal speech and mild dysmorphic features.. We identified by microarray analysis a new case of 12q15 deletion. Article Title: Constitutional chromothripsis involving chromosome 19 in a child with subtle dysmorphic features. Article Snippet: There is no conflict of interest to be reported.. Hamilton Health Sciences consider this study to be in the realm of routine clinical care instead of research on human subjects.. Correspondence to: Dr. Jia-Chi Wang, Cytogenetics Laboratory, Quest Diagnostics Nichols Institute, 33608 Ortega Highway, San Juan Capistrano, CA, 92690. Article Title: De novo unbalanced translocation leading to monosomy 9p24.3p24.1 and trisomy 19q13.42q13.43 characterized by microarray-based comparative genomic hybridization in a child with partial cortical dysplasia and craniofacial dysmorphisms without trigonocephaly. Article Snippet: De Novo Unbalanced Translocation Leading to Monosomy 9p24.3p24.1 and Trisomy 19q13.42q13.43 Characterized by Microarray-Based Comparative Genomic Hybridization in a Child With Partial Cortical Dysplasia and Craniofacial Dysmorphisms Without Trigonocephaly Nicoletta Resta,* Lucrezia De Cosmo, Francesco Claudio Susca, Donatella Capodiferro, Anna Maria Nardone, Diana Pastorivo, Marta Bertoli, Carmela Serlenga, MariaGabriella Burattini, Federico Schettini, and Nicola Laforgia Sez. di Genetica Medica, Dipartimento di Scienze Biomediche ed Oncologia Umana, Universit a degli Studi di Bari ‘‘A.. Moro’’, Bari, Italy Sez.Neonatologia e Terapia Intensiva Neonatale, Dipartimento di Ginecologia Ostetricia e Neonatologia, Universit a degli Studi di Bari ‘‘A.. Moro’’, Bari, Italy Department of Medical Genetics, Tor Vergata University of Rome, Rome, Italy Research Center and Medical Genetics Center, S. Pietro Fatebenefratelli Hospital, Rome, Italy Article Title: Carbimazole/methimazole embryopathy in siblings: a possible genetic susceptibility. Article Snippet: Her molecular karyotype using the Construct:Article Title: Poster Abstracts of the ISPD 17th International Conference on Prenatal Diagnosis and Therapy Article Snippet: .. These samples were examined by microarray-based comparative genomic hybridization (aCGH) using a 60 K |