Authors : Deng Y; Department of Medical Genetics and Prenatal Diagnosis, Sichuan Provincial Women's and Children's Hospital, The Affiliated Women's and Children's Hospital of Chengdu Medical College, Chengdu, 610031, China.; Zeng L

Subjects: Mosaicism* ; Karyotyping*/Karyotyping*/Karyotyping*/methods ; Prenatal Diagnosis*/Prenatal Diagnosis*/Prenatal Diagnosis*/methods

Source: BMC medical genomics [BMC Med Genomics] 2025 Apr 10; Vol. 18 (1), pp. 70. Date of Electronic Publication: 2025 Apr 10.Publisher: BioMed Central Country of Publication: England NLM ID: 101319628 Publication Model: Electronic Cited Medium: Internet ISSN: 1755-8794

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Academic Journal

Identification of novel cytoskeleton protein involved in spermatogenic cells and sertoli cells of non-obstructive azoospermia based on microarray and bioinformatics analysis

Authors : Danial Hashemi Karoii; Hossein Azizi; Maryam Darvari

Subjects: Male; Sertoli Cells; Research

Source: BMC Med GenomicsBMC Medical Genomics, Vol 18, Iss 1, Pp 1-26 (2025)

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Prenatal diagnosis and molecular cytogenetic analysis of pure chromosome 10p15.3 microdeletion using chromosomal microarray analysis

Authors : Na Zhang; Nan Huang; Yu’e Chen

Subjects: Male; DNA Copy Number Variations; Developmental delay

Source: BMC Med GenomicsBMC Medical Genomics, Vol 17, Iss 1, Pp 1-7 (2024)

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Prenatal diagnosis and genetic etiology analysis of talipes equinovarus by chromosomal microarray analysis

Authors : Xiaorui Xie; Baojia Huang; Linjuan Su

Subjects: Chromosome Aberrations; Single nucleotide polymorphism array; DNA Copy Number Variations

Source: BMC Med GenomicsBMC Medical Genomics, Vol 16, Iss 1, Pp 1-9 (2023)

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Evaluation of genetic variants using chromosomal microarray analysis for fetuses with polyhydramnios

Authors : Xiaoqing Wu; Ying Li; Na Lin

Subjects: Chromosome Aberrations; Polyhydramnios; 0301 basic medicine

Source: BMC Med GenomicsBMC Medical Genomics, Vol 15, Iss 1, Pp 1-7 (2022)

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Identification of key genes and miRNAs related to polycystic ovary syndrome by comprehensive analysis of microarray

Authors : Ziqian Sun; Yang Wang; Tianshu Wei

Subjects: Polycystic ovary syndrome; Differentially expressed genes; Differentially expressed miRNAs

Source: BMC Medical Genomics, Vol 15, Iss 1, Pp 1-8 (2022)

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A novel gene selection algorithm for cancer classification using microarray datasets

Authors : Russul Alanni; Jingyu Hou; Hasseeb Azzawi

Subjects: Gene selection; Gene expression programming; Support vector machine

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

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Chromosomal microarray analysis in developmental delay and intellectual disability with comorbid conditions

Authors : Yanjie Fan; Yanming Wu; Lili Wang

Subjects: Chromosomal microarray; Developmental delay; Intellectual disability

Source: BMC Medical Genomics, Vol 11, Iss 1, Pp 1-8 (2018)

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A meta-analysis of public microarray data identifies gene regulatory pathways deregulated in peripheral blood mononuclear cells from individuals with Systemic Lupus Erythematosus compared to those without

Authors : Wendy Kröger; Darlington Mapiye; Jean-Baka Domelevo Entfellner

Subjects: Lupus; Systemic Lupus Erythematosus (SLE); Microarray

Source: BMC Medical Genomics, Vol 9, Iss 1, Pp 1-11 (2016)

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A combined linkage, microarray and exome analysis suggests MAP3K11 as a candidate gene for left ventricular hypertrophy

Authors : Najaf Amin; Ayse Demirkan; Laura B. Piñeros-Hernández

Subjects: Male; Exome sequencing; 0301 basic medicine

Source: BMC Med GenomicsBMC Medical Genomics, Vol 11, Iss 1, Pp 1-10 (2018)Benjamin, E.J., Levy, D., Why is left ventricular hypertrophy so predictive of morbidity

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نتائج البحث

فلترة النتائج

Effective detection of 148 cases chromosomal mosaicism by karyotyping, chromosomal microarray analysis and QF-PCR in 32,967 prenatal diagnoses.

Identification of novel cytoskeleton protein involved in spermatogenic cells and sertoli cells of non-obstructive azoospermia based on microarray and bioinformatics analysis

Prenatal diagnosis and molecular cytogenetic analysis of pure chromosome 10p15.3 microdeletion using chromosomal microarray analysis

Prenatal diagnosis and genetic etiology analysis of talipes equinovarus by chromosomal microarray analysis

Evaluation of genetic variants using chromosomal microarray analysis for fetuses with polyhydramnios

Identification of key genes and miRNAs related to polycystic ovary syndrome by comprehensive analysis of microarray

A novel gene selection algorithm for cancer classification using microarray datasets

Chromosomal microarray analysis in developmental delay and intellectual disability with comorbid conditions

A meta-analysis of public microarray data identifies gene regulatory pathways deregulated in peripheral blood mononuclear cells from individuals with Systemic Lupus Erythematosus compared to those without

A combined linkage, microarray and exome analysis suggests MAP3K11 as a candidate gene for left ventricular hypertrophy

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