Correction: Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes
Sadikovic, Bekim, Wang, Jing, El-Hattab, Ayman W, Landsverk, Megan, Douglas, Ganka, Brundage, Ellen K, Craigen, William J, Schmitt, Eric S, Wong, Lee-Jun C
Published in PloS one (20.11.2017)
Published in PloS one (20.11.2017)
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Sequence homology at the breakpoint and clinical phenotype of mitochondrial DNA deletion syndromes
Sadikovic, Bekim, Wang, Jing, El-Hattab, Ayman W, Landsverk, Megan, Douglas, Ganka, Brundage, Ellen K, Craigen, William J, Schmitt, Eric S, Wong, Lee-Jun C
Published in PloS one (20.12.2010)
Published in PloS one (20.12.2010)
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Utility of Oligonucleotide Array-Based Comparative Genomic Hybridization for Detection of Target Gene Deletions
Wong, Lee-Jun C, Dimmock, David, Geraghty, Michael T, Quan, Richard, Lichter-Konecki, Uta, Wang, Jing, Brundage, Ellen K, Scaglia, Fernando, Chinault, A. Craig
Published in Clinical chemistry (Baltimore, Md.) (01.07.2008)
Published in Clinical chemistry (Baltimore, Md.) (01.07.2008)
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Application of dual-genome oligonucleotide array-based comparative genomic hybridization to the molecular diagnosis of mitochondrial DNA deletion and depletion syndromes
Chinault, A Craig, Shaw, Chad A, Brundage, Ellen K, Tang, Lin-Ya, Wong, Lee-Jun C
Published in Genetics in medicine (01.07.2009)
Published in Genetics in medicine (01.07.2009)
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HERV‐mediated genomic rearrangement of EYA1 in an individual with branchio‐oto‐renal syndrome
Sanchez‐Valle, Amarilis, Wang, Xueqing, Potocki, Lorraine, Xia, Zhilian, Kang, Sung‐Hae L., Carlin, Mary E., Michel, Donnice, Williams, Patricia, Cabrera‐Meza, Gerardo, Brundage, Ellen K., Eifert, Anna L., Stankiewicz, Pawel, Cheung, Sau Wai, Lalani, Seema R.
Published in American journal of medical genetics. Part A (01.11.2010)
Published in American journal of medical genetics. Part A (01.11.2010)
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HERV-Mediated Genomic Rearrangement of εYA1 in an individual With Branchio-oto-renal Syndrome
SANCHEZ-VALLE, Amarilis, XUEQING WANG, EIFERT, Anna L, STANKIEWICZ, Pawel, SAU WAI CHEUNG, LALANI, Seema R, POTOCKI, Lorraine, ZHILIAN XIA, KANG, Sung-Hae L, CARLIN, Mary E, MICHEL, Donnice, WILLIAMS, Patricia, CABRERA-MEZA, Gerardo, BRUNDAGE, Ellen K
Published in American journal of medical genetics. Part A (01.11.2010)
Published in American journal of medical genetics. Part A (01.11.2010)
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Cornelia de Lange syndrome case due to genomic rearrangements including NIPBL
Ratajska, Magdalena, Wierzba, Jolanta, Pehlivan, Davut, Xia, Zhilian, Brundage, Ellen K, Cheung, Sau Wai, Stankiewicz, Pawel, Lupski, James R, Limon, Janusz
Published in European journal of medical genetics (01.11.2010)
Published in European journal of medical genetics (01.11.2010)
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A novel chromosome 19p13.12 deletion in a child with multiple congenital anomalies
Jensen, Daniel R., Martin, Donna M., Gebarski, Stephen, Sahoo, Trilochan, Brundage, Ellen K., Chinault, A. Craig, Otto, Edgar A., Chaki, Moumita, Hildebrandt, Friedhelm, Cheung, Sau Wai, Lesperance, Marci M.
Published in American journal of medical genetics. Part A (01.03.2009)
Published in American journal of medical genetics. Part A (01.03.2009)
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Molecular characterization of CPS1 deletions by array CGH
Wang, Jing, Shchelochkov, Oleg A., Zhan, Hongli, Li, Fangyuan, Chen, Li-Chieh, Brundage, Ellen K., Pursley, Amber N., Schmitt, Eric S., Häberle, Johannes, Wong, Lee-Jun C.
Published in Molecular genetics and metabolism (01.01.2011)
Published in Molecular genetics and metabolism (01.01.2011)
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Application of oligonucleotide array CGH to the simultaneous detection of a deletion in the nuclear TK2 gene and mtDNA depletion
Zhang, Shulin, Li, Fang-yuan, Bass, Harold N., Pursley, Amber, Schmitt, Eric S., Brown, Blaire L., Brundage, Ellen K., Mardach, Rebecca, Wong, Lee-Jun
Published in Molecular genetics and metabolism (2010)
Published in Molecular genetics and metabolism (2010)
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Application of oligonucleotide array CGH in the detection of a large intragenic deletion in POLG associated with Alpers Syndrome
Compton, Alison G, Troedson, Christopher, Wilson, Meredith, Procopis, Peter G, Li, Fang-Yuan, Brundage, Ellen K, Yamazaki, Taro, Thorburn, David R, Wong, Lee-Jun C
Published in Mitochondrion (01.01.2011)
Published in Mitochondrion (01.01.2011)
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Journal Article
Application of dual-genome oligonucleotidearray-based comparative genomic hybridization to the molecular diagnosis of mitochondrial DNA deletion and depletion syndromes
Chinault, A. Craig, Shaw, Chad A., Brundage, Ellen K., Tang, Lin-Ya, Wong, Lee-Jun C.
Published in Genetics in medicine (01.07.2009)
Published in Genetics in medicine (01.07.2009)
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20p12.3 microdeletion predisposes to Wolff–Parkinson–White syndrome with variable neurocognitive deficits
Lalani, S R, Thakuria, J V, Cox, G F, Wang, X, Bi, W, Bray, M S, Shaw, C, Cheung, S W, Chinault, A C, Boggs, B A, Ou, Z, Brundage, E K, Lupski, J R, Gentile, J, Waisbren, S, Pursley, A, Ma, L, Khajavi, M, Zapata, G, Friedman, R, Kim, J J, Towbin, J A, Stankiewicz, P, Schnittger, S, Hansmann, I, Ai, T, Sood, S, Wehrens, X H, Martin, J F, Belmont, J W, Potocki, L
Published in Journal of medical genetics (01.03.2009)
Published in Journal of medical genetics (01.03.2009)
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Journal Article
HERV-mediated genomic rearrangement of EYA1 in an individual with branchio-oto-renal syndrome
Sanchez-Valle, Amarilis, Wang, Xueqing, Potocki, Lorraine, Xia, Zhilian, Kang, Sung-Hae L., Carlin, Mary E., Michel, Donnice, Williams, Patricia, Cabrera-Meza, Gerardo, Brundage, Ellen K., Eifert, Anna L., Stankiewicz, Pawel, Cheung, Sau Wai, Lalani, Seema R.
Published in American Journal of Medical Genetics Part A (01.11.2010)
Published in American Journal of Medical Genetics Part A (01.11.2010)
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