Identification of Small Regions of Overlap from Copy Number Variable Regions in Patients with Hypospadias

Identification of Small Regions of Overlap from Copy Number Variable Regions in Patients with Hypospadias

Show other versions (1)

Hypospadias is a common form of congenital atypical sex development that is often associated with other congenital comorbidities. Many genes have been associated with the condition, most commonly single sequence variations. Further investigations of recurrent and overlapping copy number variations (...

Full description

Bibliographic Details
Main Authors:	Amarillo, I.E (Author), Scott, C.H (Author)
Format:	Article
Language:	English
Published:	MDPI 2022
Subjects:	CNV map differences of sex development DNA copy number variations hypospadias microarray analysis small regions of overlap
Online Access:	View Fulltext in Publisher

Similar Items

Identification of Small Regions of Overlap from Copy Number Variable Regions in Patients with Hypospadias
by: Amarillo, I.E, et al.
Published: (2022)

A method to assess linkage disequilibrium between CNVs and SNPs inside copy number variable regions
by: Nathan E Wineinger, et al.
Published: (2011-04-01)

A Potential Method to Help Predict Genetic Diseases and Arrange Healthcare: Copy Number Variation Analysis
by: Munis Dündar, et al.
Published: (2019-11-01)

The Role of Number of Copies, Structure, Behavior and Copy Number Variations (CNV) of the Y Chromosome in Male Infertility
by: Fabrizio Signore, et al.
Published: (2019-12-01)

Comparative analyses of copy number variations between Bos taurus and Bos indicus
by: Yan Hu, et al.
Published: (2020-10-01)

A Rapid PCR-Free Next-Generation Sequencing Method for the Detection of Copy Number Variations in Prenatal Samples
by: Xiya Zhou, et al.
Published: (2021-01-01)

Total copy number variation as a prognostic factor in adult astrocytoma subtypes
by: Kanish Mirchia, et al.
Published: (2019-06-01)

Analysis of Genomic Copy Number Variation in Miscarriages During Early and Middle Pregnancy
by: Heming Wu, et al.
Published: (2021-09-01)

Genome-wide copy number variations in a large cohort of bantu African children
by: Feyza Yilmaz, et al.
Published: (2021-05-01)

Establishing a prognostic threshold for total copy number variation within adult IDH-mutant grade II/III astrocytomas
by: Kanish Mirchia, et al.
Published: (2019-07-01)

Population differentiated copy number variation of Bos taurus, Bos indicus and their African hybrids
by: Jisung Jang, et al.
Published: (2021-07-01)

Copy Number Variation Analysis in the Context of Electronic Medical Records & Large-Scale Genomics Consortium Efforts
by: John J Connolly, et al.
Published: (2014-03-01)

Copy Number Studies in Noisy Samples
by: Caspar Grond-Ginsbach, et al.
Published: (2013-11-01)

Copy Number Variation of the PIGY Gene in Sheep and Its Association Analysis with Growth Traits
by: Ziting Feng, et al.
Published: (2020-04-01)

Complement C4 Gene Copy Number Variation Genotyping by High Resolution Melting PCR
by: Claudia P. Jaimes-Bernal, et al.
Published: (2020-08-01)

Detection of copy number variation and selection signatures on the X chromosome in Chinese indigenous sheep with different types of tail
by: Caiye Zhu, et al.
Published: (2020-09-01)

Variation of DNA copies number in etiology of congenital heart defects
by: A. A. Slepukhina, et al.
Published: (2018-11-01)

Copy Number Variation: Methods and Clinical Applications
by: Ondrej Pös, et al.
Published: (2021-01-01)

Influence of validating the parental origin on the clinical interpretation of fetal copy number variations in 141 core family cases
by: Panlai Shi, et al.
Published: (2019-10-01)

Copy Number Variants in Four Italian Turkey Breeds
by: Maria Giuseppina Strillacci, et al.
Published: (2021-02-01)

Copy Number Variation in Monozygotic Twins with NF1
by: Sites, Emily
Published: (2010)

Gene expression patterns of chicken neuregulin 3 in association with copy number variation and frameshift deletion
by: Hideaki Abe, et al.
Published: (2017-07-01)

Copy number variation of Ppd-B1 is the major determinant of heading time in durum wheat
by: Tobias Würschum, et al.
Published: (2019-07-01)

Platform comparison of detecting copy number variants with microarrays and whole-exome sequencing
by: Joep de Ligt, et al.
Published: (2014-12-01)

Copy Number Variation in SOX6 Contributes to Chicken Muscle Development
by: Shudai Lin, et al.
Published: (2018-01-01)

Fine mapping of copy number variations on two cattle genome assemblies using high density SNP array
by: Hou Yali, et al.
Published: (2012-08-01)

Copy Number Variation of the CADM2 Gene and Its Association with Growth Traits in Yak
by: Fei Ge, et al.
Published: (2019-11-01)

Integrated CNV-seq, karyotyping and SNP-array analyses for effective prenatal diagnosis of chromosomal mosaicism
by: Na Ma, et al.
Published: (2021-02-01)

E2F1 copy number variations in germline and breast cancer: a retrospective study of 222 Italian women
by: Maria Santa Rocca, et al.
Published: (2021-03-01)

Copy Number Variation of the <i>SHE</i> Gene in Sheep and Its Association with Economic Traits
by: Rui Jiang, et al.
Published: (2019-08-01)

SRBreak: A read-depth and split-read framework to identify breakpoints of different events inside simple copy-number variable regions
by: HOANG T NGUYEN, et al.
Published: (2016-09-01)

High resolution measurement of DUF1220 domain copy number from whole genome sequence data
by: David P. Astling, et al.
Published: (2017-08-01)

Inferring Variation in Copy Number Using High Throughput Sequencing Data in R
by: Brian J. Knaus, et al.
Published: (2018-04-01)

Copy number variations associated with fetal congenital kidney malformations
by: Meiying Cai, et al.
Published: (2020-03-01)

Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans
by: Rajini R. Haraksingh, et al.
Published: (2017-04-01)

Identification of Copy Number Variants in a Southern Chinese Cohort of Patients with Congenital Scoliosis
by: Wenjing Lai, et al.
Published: (2021-08-01)

Use of the MLPA Assay in the Molecular Diagnosis of Gene Copy Number Alterations in Human Genetic Diseases
by: Valentina Gatta, et al.
Published: (2012-03-01)

Landscape of copy number aberrations in esophageal squamous cell carcinoma from a high endemic region of South Africa
by: Jacqueline Brown, et al.
Published: (2020-04-01)

A survey of analysis software for array-comparative genomic hybridisation studies to detect copy number variation
by: Karimpour-Fard Anis, et al.
Published: (2010-08-01)

Performances of NIPT for copy number variations at different sequencing depths using the semiconductor sequencing platform
by: Jiexia Yang, et al.
Published: (2021-07-01)

Cannot write session to /tmp/vufind_sessions/sess_drlt2erecdlfsj9th82lu1gplj