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Correction: Evaluation of the Genetic Basis of Familial Aggregation of Pacemaker Implantation by a Large Next Generation Sequencing Panel.

PloS one

Celestino-Soper PB, Doytchinova A, Steiner HA, Uradu A, Lynnes TC, Groh WJ, Miller JM, Lin H, Gao H, Wang Z, Liu Y, Chen PS, Vatta M.
PMID: 26771585
PLoS One. 2016 Jan 15;11(1):e0147455. doi: 10.1371/journal.pone.0147455. eCollection 2016.

No abstract available.

Cite
Celestino-Soper PB, Doytchinova A, Steiner HA, et al. Correction: Evaluation of the Genetic Basis of Familial Aggregation of Pacemaker Implantation by a Large Next Generation Sequencing Panel. PLoS One. 2016;11(1):e0147455doi: 10.1371/journal.pone.0147455.
Celestino-Soper, P. B., Doytchinova, A., Steiner, H. A., Uradu, A., Lynnes, T. C., Groh, W. J., Miller, J. M., Lin, H., Gao, H., Wang, Z., Liu, Y., Chen, P. S., & Vatta, M. (2016). Correction: Evaluation of the Genetic Basis of Familial Aggregation of Pacemaker Implantation by a Large Next Generation Sequencing Panel. PloS one, 11(1), e0147455. https://doi.org/10.1371/journal.pone.0147455
Celestino-Soper, Patrícia B S, et al. "Correction: Evaluation of the Genetic Basis of Familial Aggregation of Pacemaker Implantation by a Large Next Generation Sequencing Panel." PloS one vol. 11,1 (2016): e0147455. doi: https://doi.org/10.1371/journal.pone.0147455
Celestino-Soper PB, Doytchinova A, Steiner HA, Uradu A, Lynnes TC, Groh WJ, Miller JM, Lin H, Gao H, Wang Z, Liu Y, Chen PS, Vatta M. Correction: Evaluation of the Genetic Basis of Familial Aggregation of Pacemaker Implantation by a Large Next Generation Sequencing Panel. PLoS One. 2016 Jan 15;11(1):e0147455. doi: 10.1371/journal.pone.0147455. eCollection 2016. PMID: 26771585; PMCID: PMC4714943.
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Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders.

Molecular cytogenetics

Celestino-Soper PB, Skinner C, Schroer R, Eng P, Shenai J, Nowaczyk MM, Terespolsky D, Cushing D, Patel GS, Immken L, Willis A, Wiszniewska J, Matalon R, Rosenfeld JA, Stevenson RE, Kang SH, Cheung SW, Beaudet AL, Stankiewicz P.
PMID: 22480366
Mol Cytogenet. 2012 Apr 05;5:17. doi: 10.1186/1755-8166-5-17.

Interstitial deletions of the short arm of chromosome 6 are rare and have been associated with developmental delay, hypotonia, congenital anomalies, and dysmorphic features. We used array comparative genomic hybridization in a South Carolina Autism Project (SCAP) cohort of...

Cite
Celestino-Soper PB, Skinner C, Schroer R, et al. Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders. Mol Cytogenet. 2012;5:17doi: 10.1186/1755-8166-5-17.
Celestino-Soper, P. B., Skinner, C., Schroer, R., Eng, P., Shenai, J., Nowaczyk, M. M., Terespolsky, D., Cushing, D., Patel, G. S., Immken, L., Willis, A., Wiszniewska, J., Matalon, R., Rosenfeld, J. A., Stevenson, R. E., Kang, S. H., Cheung, S. W., Beaudet, A. L., & Stankiewicz, P. (2012). Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders. Molecular cytogenetics, 517. https://doi.org/10.1186/1755-8166-5-17
Celestino-Soper, Patrícia Bs, et al. "Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders." Molecular cytogenetics vol. 5 (2012): 17. doi: https://doi.org/10.1186/1755-8166-5-17
Celestino-Soper PB, Skinner C, Schroer R, Eng P, Shenai J, Nowaczyk MM, Terespolsky D, Cushing D, Patel GS, Immken L, Willis A, Wiszniewska J, Matalon R, Rosenfeld JA, Stevenson RE, Kang SH, Cheung SW, Beaudet AL, Stankiewicz P. Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders. Mol Cytogenet. 2012 Apr 05;5:17. doi: 10.1186/1755-8166-5-17. PMID: 22480366; PMCID: PMC3351998.
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Validation and Utilization of a Clinical Next-Generation Sequencing Panel for Selected Cardiovascular Disorders.

Frontiers in cardiovascular medicine

Celestino-Soper PB, Gao H, Lynnes TC, Lin H, Liu Y, Spoonamore KG, Chen PS, Vatta M.
PMID: 28361054
Front Cardiovasc Med. 2017 Mar 15;4:11. doi: 10.3389/fcvm.2017.00011. eCollection 2017.

The development of high-throughput technologies such as next-generation sequencing (NGS) has allowed for thousands of DNA loci to be interrogated simultaneously in a fast and economical method for the detection of clinically deleterious variants. Whenever a clinical diagnosis is...

Cite
Celestino-Soper PB, Gao H, Lynnes TC, et al. Validation and Utilization of a Clinical Next-Generation Sequencing Panel for Selected Cardiovascular Disorders. Front Cardiovasc Med. 2017;4:11doi: 10.3389/fcvm.2017.00011.
Celestino-Soper, P. B., Gao, H., Lynnes, T. C., Lin, H., Liu, Y., Spoonamore, K. G., Chen, P. S., & Vatta, M. (2017). Validation and Utilization of a Clinical Next-Generation Sequencing Panel for Selected Cardiovascular Disorders. Frontiers in cardiovascular medicine, 411. https://doi.org/10.3389/fcvm.2017.00011
Celestino-Soper, Patrícia B S, et al. "Validation and Utilization of a Clinical Next-Generation Sequencing Panel for Selected Cardiovascular Disorders." Frontiers in cardiovascular medicine vol. 4 (2017): 11. doi: https://doi.org/10.3389/fcvm.2017.00011
Celestino-Soper PB, Gao H, Lynnes TC, Lin H, Liu Y, Spoonamore KG, Chen PS, Vatta M. Validation and Utilization of a Clinical Next-Generation Sequencing Panel for Selected Cardiovascular Disorders. Front Cardiovasc Med. 2017 Mar 15;4:11. doi: 10.3389/fcvm.2017.00011. eCollection 2017. PMID: 28361054; PMCID: PMC5350117.
Copy Download .nbib Format: NLM
Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders.

Molecular cytogenetics

Celestino-Soper PB, Skinner C, Schroer R, Eng P, Shenai J, Nowaczyk MM, Terespolsky D, Cushing D, Patel GS, Immken L, Willis A, Wiszniewska J, Matalon R, Rosenfeld JA, Stevenson RE, Kang SH, Cheung SW, Beaudet AL, Stankiewicz P.
PMID: 22480366
Mol Cytogenet. 2012 Apr 05;5:17. doi: 10.1186/1755-8166-5-17.

Interstitial deletions of the short arm of chromosome 6 are rare and have been associated with developmental delay, hypotonia, congenital anomalies, and dysmorphic features. We used array comparative genomic hybridization in a South Carolina Autism Project (SCAP) cohort of...

Cite
Celestino-Soper PB, Skinner C, Schroer R, et al. Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders. Mol Cytogenet. 2012;5:17doi: 10.1186/1755-8166-5-17.
Celestino-Soper, P. B., Skinner, C., Schroer, R., Eng, P., Shenai, J., Nowaczyk, M. M., Terespolsky, D., Cushing, D., Patel, G. S., Immken, L., Willis, A., Wiszniewska, J., Matalon, R., Rosenfeld, J. A., Stevenson, R. E., Kang, S. H., Cheung, S. W., Beaudet, A. L., & Stankiewicz, P. (2012). Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders. Molecular cytogenetics, 517. https://doi.org/10.1186/1755-8166-5-17
Celestino-Soper, Patrícia Bs, et al. "Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders." Molecular cytogenetics vol. 5 (2012): 17. doi: https://doi.org/10.1186/1755-8166-5-17
Celestino-Soper PB, Skinner C, Schroer R, Eng P, Shenai J, Nowaczyk MM, Terespolsky D, Cushing D, Patel GS, Immken L, Willis A, Wiszniewska J, Matalon R, Rosenfeld JA, Stevenson RE, Kang SH, Cheung SW, Beaudet AL, Stankiewicz P. Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders. Mol Cytogenet. 2012 Apr 05;5:17. doi: 10.1186/1755-8166-5-17. PMID: 22480366; PMCID: PMC3351998.
Copy Download .nbib Format: NLM
Showing 1 to 4 of 4 entries