نتائج البحث

The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay.

• Authors : Wayhelova M; Institute of Experimental Biology, Faculty of Science, Masaryk University, Kotlarska 267/2, Brno, Czech Republic. .; Department of Medical Genetics, University Hospital Brno, Cernopolni 212/9, Brno, Czech Republic. .

Subjects: Comparative Genomic Hybridization* ; DNA Copy Number Variations* ; Oligonucleotide Array Sequence Analysis*

• Source: BMC medical genomics [BMC Med Genomics] 2019 Jul 23; Vol. 12 (1), pp. 111. Date of Electronic Publication: 2019 Jul 23.Publisher: BioMed Central Country of Publication: England NLM ID: 101319628 Publication Model: Electronic Cited Medium: Internet ISSN: 1755-8794

تفاصيل العنوان

Randomized comparison of next-generation sequencing and array comparative genomic hybridization for preimplantation genetic screening: a pilot study.

• Authors : Zhihong Yang^1,2,3 ; James Lin²; Zhang, John⁴

• Source: BMC Medical Genomics. 2015, Vol. 8 Issue 1, p1-13. 13p.

تفاصيل العنوان

The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay

• Authors : Marketa Wayhelova; Jan Smetana; Vladimira Vallova

Subjects: Intellectual disability; Developmental delay; Microdeletion

• Source: BMC Medical Genomics, Vol 12, Iss 1, Pp 1-11 (2019)

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Clinicopathological investigation of secretory carcinoma cases including a successful treatment outcome using entrectinib for high-grade transformation: a case report.

• Authors : Suzuki, Kensuke¹ (AUTHOR) ; Harada, Hiroshi² (AUTHOR); Takeda, Masayuki³ (AUTHOR)

• Source: BMC Medical Genomics. 1/6/2022, Vol. 15 Issue 1, p1-13. 13p.

تفاصيل العنوان

Randomized comparison of next-generation sequencing and array comparative genomic hybridization for preimplantation genetic screening: a pilot study.

• Authors : Yang Z; ZytoGen Global Genetics Institute, Timonium, MD, USA. .; Reproductive Fertility Center, Irvine, CA, USA. .

Subjects: Aneuploidy* ; Comparative Genomic Hybridization* ; High-Throughput Nucleotide Sequencing*

• Source: BMC medical genomics [BMC Med Genomics] 2015 Jun 23; Vol. 8, pp. 30. Date of Electronic Publication: 2015 Jun 23.Publisher: BioMed Central Country of Publication: England NLM ID: 101319628 Publication Model: Electronic Cited Medium: Internet ISSN: 1755-8794

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12q14 microduplication: a new clinical entity reciprocal to the microdeletion syndrome?

• Authors : Dória, Sofia^1,2 (AUTHOR) ; Alves, Daniela³ (AUTHOR); Pinho, Maria João^1,2 (AUTHOR)

• Source: BMC Medical Genomics. 1/3/2020, Vol. 13 Issue 1, p1-6. 6p.

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A new family with spastic paraplegia type 51 and novel mutations in AP4E1.

• Authors : Winkler, Izabela^1,2 (AUTHOR) ; Miotła, Paweł² (AUTHOR); Lejman, Monika³ (AUTHOR)

• Source: BMC Medical Genomics. 5/18/2021, Vol. 14 Issue 1, p1-6. 6p.

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Error-corrected sequencing strategies enable comprehensive detection of leukemic mutations relevant for diagnosis and minimal residual disease monitoring.

• Authors : Crowgey, Erin L.¹ (AUTHOR); Mahajan, Nitin^2,3 (AUTHOR); Wong, Wing Hing^2,3 (AUTHOR)

• Source: BMC Medical Genomics. 3/4/2020, Vol. 13 Issue 1, p1-11. 11p.

تفاصيل العنوان

Hybridization and amplification rate correction for affymetrix SNP arrays.

• Authors : Wang, Quan¹; Peng, Peichao²; Qian, Minping^1,2

• Source: BMC Medical Genomics. 2012, Vol. 5 Issue 1, p24-32. 9p. 4 Diagrams, 1 Chart.

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Correlating genomic copy number alterations with clinicopathologic findings in 75 cases of hepatocellular carcinoma.

• Authors : Peng, Gang^1,2 (AUTHOR); Chai, Hongyan² (AUTHOR); Ji, Weizhen² (AUTHOR)

• Source: BMC Medical Genomics. 6/8/2021, Vol. 14 Issue 1, p1-9. 9p.

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