Erratum: Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and digeorge syndromes (American Journal of Human Genetics (2013) 92 (439-447))

Maria Delio; Tingwei Guo; Donna M. McDonald-Mcginn; Elaine Zackai; Sean Herman; Mark Kaminetzky; Anne Marie Higgins; Karlene Coleman; Carolyn Chow; Maria Jalbrzikowski; Carrie E. Bearden; Alice Bailey; Anders Vangkilde; Line Olsen; Charlotte Olesen; Flemming Skovby; Thomas M. Werge; Ludivine Templin; Tiffany Busa; Nicole Philip; Ann Swillen; Joris R. Vermeesch; Koen Devriendt; Maude Schneider; Sophie Dahoun; Stephan Eliez; Kelly Schoch; Stephen R. Hooper; Vandana Shashi; Joy Samanich; Robert Marion; Therese Van Amelsvoort; Erik Boot; Petra Klaassen; Sasja N. Duijff; Jacob Vorstman; Tracy Yuen; Candice Silversides; Eva Chow; Anne Bassett; Amos Frisch; Abraham Weizman; Doron Gothelf; Maria Niarchou; Marianne Van Den Bree; Michael J. Owen; Damian Heine Suñer; Jordi Rosell Andreo; Marco Armando; Stefano Vicari; Maria Cristina Digilio; Adam Auton; Wendy R. Kates; Tao Wang; Robert J. Shprintzen; Beverly S. Emanuel; Bernice E. Morrow

doi:10.1016/j.ajhg.2013.03.005

Erratum: Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and digeorge syndromes (American Journal of Human Genetics (2013) 92 (439-447))

Maria Delio, Tingwei Guo, Donna M. McDonald-Mcginn, Elaine Zackai, Sean Herman, Mark Kaminetzky, Anne Marie Higgins, Karlene Coleman, Carolyn Chow, Maria Jalbrzikowski, Carrie E. Bearden, Alice Bailey, Anders Vangkilde, Line Olsen, Charlotte Olesen, Flemming Skovby, Thomas M. Werge, Ludivine Templin, Tiffany Busa, Nicole PhilipAnn Swillen, Joris R. Vermeesch, Koen Devriendt, Maude Schneider, Sophie Dahoun, Stephan Eliez, Kelly Schoch, Stephen R. Hooper, Vandana Shashi, Joy Samanich, Robert Marion, Therese Van Amelsvoort, Erik Boot, Petra Klaassen, Sasja N. Duijff, Jacob Vorstman, Tracy Yuen, Candice Silversides, Eva Chow, Anne Bassett, Amos Frisch, Abraham Weizman, Doron Gothelf, Maria Niarchou, Marianne Van Den Bree, Michael J. Owen, Damian Heine Suñer, Jordi Rosell Andreo, Marco Armando, Stefano Vicari, Maria Cristina Digilio, Adam Auton, Wendy R. Kates, Tao Wang, Robert J. Shprintzen, Beverly S. Emanuel, Bernice E. Morrow^*

^*Corresponding author for this work

Research output: Contribution to journal › Comment/debate

Original language	English
Pages (from-to)	637
Number of pages	1
Journal	American Journal of Human Genetics
Volume	92
Issue number	4
DOIs	https://doi.org/10.1016/j.ajhg.2013.03.005
State	Published - 4 Apr 2013

Access to Document

10.1016/j.ajhg.2013.03.005

Cite this

Delio, M., Guo, T., McDonald-Mcginn, D. M., Zackai, E., Herman, S., Kaminetzky, M., Higgins, A. M., Coleman, K., Chow, C., Jalbrzikowski, M., Bearden, C. E., Bailey, A., Vangkilde, A., Olsen, L., Olesen, C., Skovby, F., Werge, T. M., Templin, L., Busa, T., ... Morrow, B. E. (2013). Erratum: Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and digeorge syndromes (American Journal of Human Genetics (2013) 92 (439-447)). American Journal of Human Genetics, 92(4), 637. https://doi.org/10.1016/j.ajhg.2013.03.005

@article{2e74c6ed374141d89133c6b1db56d818,

title = "Erratum: Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and digeorge syndromes (American Journal of Human Genetics (2013) 92 (439-447))",

author = "Maria Delio and Tingwei Guo and McDonald-Mcginn, {Donna M.} and Elaine Zackai and Sean Herman and Mark Kaminetzky and Higgins, {Anne Marie} and Karlene Coleman and Carolyn Chow and Maria Jalbrzikowski and Bearden, {Carrie E.} and Alice Bailey and Anders Vangkilde and Line Olsen and Charlotte Olesen and Flemming Skovby and Werge, {Thomas M.} and Ludivine Templin and Tiffany Busa and Nicole Philip and Ann Swillen and Vermeesch, {Joris R.} and Koen Devriendt and Maude Schneider and Sophie Dahoun and Stephan Eliez and Kelly Schoch and Hooper, {Stephen R.} and Vandana Shashi and Joy Samanich and Robert Marion and {Van Amelsvoort}, Therese and Erik Boot and Petra Klaassen and Duijff, {Sasja N.} and Jacob Vorstman and Tracy Yuen and Candice Silversides and Eva Chow and Anne Bassett and Amos Frisch and Abraham Weizman and Doron Gothelf and Maria Niarchou and {Van Den Bree}, Marianne and Owen, {Michael J.} and Su{\~n}er, {Damian Heine} and Andreo, {Jordi Rosell} and Marco Armando and Stefano Vicari and Digilio, {Maria Cristina} and Adam Auton and Kates, {Wendy R.} and Tao Wang and Shprintzen, {Robert J.} and Emanuel, {Beverly S.} and Morrow, {Bernice E.}",

year = "2013",

month = apr,

day = "4",

doi = "10.1016/j.ajhg.2013.03.005",

language = "אנגלית",

volume = "92",

pages = "637",

journal = "American Journal of Human Genetics",

issn = "0002-9297",

publisher = "Cell Press",

number = "4",

}

Delio, M, Guo, T, McDonald-Mcginn, DM, Zackai, E, Herman, S, Kaminetzky, M, Higgins, AM, Coleman, K, Chow, C, Jalbrzikowski, M, Bearden, CE, Bailey, A, Vangkilde, A, Olsen, L, Olesen, C, Skovby, F, Werge, TM, Templin, L, Busa, T, Philip, N, Swillen, A, Vermeesch, JR, Devriendt, K, Schneider, M, Dahoun, S, Eliez, S, Schoch, K, Hooper, SR, Shashi, V, Samanich, J, Marion, R, Van Amelsvoort, T, Boot, E, Klaassen, P, Duijff, SN, Vorstman, J, Yuen, T, Silversides, C, Chow, E, Bassett, A, Frisch, A, Weizman, A , Gothelf, D, Niarchou, M, Van Den Bree, M, Owen, MJ, Suñer, DH, Andreo, JR, Armando, M, Vicari, S, Digilio, MC, Auton, A, Kates, WR, Wang, T, Shprintzen, RJ, Emanuel, BS & Morrow, BE 2013, 'Erratum: Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and digeorge syndromes (American Journal of Human Genetics (2013) 92 (439-447))', American Journal of Human Genetics, vol. 92, no. 4, pp. 637. https://doi.org/10.1016/j.ajhg.2013.03.005

TY - JOUR

T1 - Erratum

T2 - Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and digeorge syndromes (American Journal of Human Genetics (2013) 92 (439-447))

AU - Delio, Maria

AU - Guo, Tingwei

AU - McDonald-Mcginn, Donna M.

AU - Zackai, Elaine

AU - Herman, Sean

AU - Kaminetzky, Mark

AU - Higgins, Anne Marie

AU - Coleman, Karlene

AU - Chow, Carolyn

AU - Jalbrzikowski, Maria

AU - Bearden, Carrie E.

AU - Bailey, Alice

AU - Vangkilde, Anders

AU - Olsen, Line

AU - Olesen, Charlotte

AU - Skovby, Flemming

AU - Werge, Thomas M.

AU - Templin, Ludivine

AU - Busa, Tiffany

AU - Philip, Nicole

AU - Swillen, Ann

AU - Vermeesch, Joris R.

AU - Devriendt, Koen

AU - Schneider, Maude

AU - Dahoun, Sophie

AU - Eliez, Stephan

AU - Schoch, Kelly

AU - Hooper, Stephen R.

AU - Shashi, Vandana

AU - Samanich, Joy

AU - Marion, Robert

AU - Van Amelsvoort, Therese

AU - Boot, Erik

AU - Klaassen, Petra

AU - Duijff, Sasja N.

AU - Vorstman, Jacob

AU - Yuen, Tracy

AU - Silversides, Candice

AU - Chow, Eva

AU - Bassett, Anne

AU - Frisch, Amos

AU - Weizman, Abraham

AU - Gothelf, Doron

AU - Niarchou, Maria

AU - Van Den Bree, Marianne

AU - Owen, Michael J.

AU - Suñer, Damian Heine

AU - Andreo, Jordi Rosell

AU - Armando, Marco

AU - Vicari, Stefano

AU - Digilio, Maria Cristina

AU - Auton, Adam

AU - Kates, Wendy R.

AU - Wang, Tao

AU - Shprintzen, Robert J.

AU - Emanuel, Beverly S.

AU - Morrow, Bernice E.

PY - 2013/4/4

Y1 - 2013/4/4

UR - http://www.scopus.com/inward/record.url?scp=84875914849&partnerID=8YFLogxK

U2 - 10.1016/j.ajhg.2013.03.005

DO - 10.1016/j.ajhg.2013.03.005

M3 - ???researchoutput.researchoutputtypes.contributiontojournal.comment???

AN - SCOPUS:84875914849

SN - 0002-9297

VL - 92

SP - 637

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

IS - 4

ER -

Erratum: Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and digeorge syndromes (American Journal of Human Genetics (2013) 92 (439-447))

Access to Document

Other files and links

Cite this