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Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes. / Delio, Maria; Guo, Tingwei; McDonald-McGinn, Donna M; Zackai, Elaine; Herman, Sean; Kaminetzky, Mark; Higgins, Anne Marie; Coleman, Karlene; Chow, Carolyn; Jalbrzikowski, Maria; Jarlbrzkowski, Maria; Bearden, Carrie E; Bailey, Alice; Vangkilde, Anders; Olsen, Line; Olesen, Charlotte; Skovby, Flemming; Werge, Thomas M; Templin, Ludivine; Busa, Tiffany; Philip, Nicole; Swillen, Ann; Vermeesch, Joris R; Devriendt, Koen; Schneider, Maude; Dahoun, Sophie; Eliez, Stephan; Schoch, Kelly; Hooper, Stephen R; Shashi, Vandana; Samanich, Joy; Marion, Robert; van Amelsvoort, Therese; Boot, Erik; Klaassen, Petra; Duijff, Sasja N; Vorstman, Jacob; Yuen, Tracy; Silversides, Candice; Chow, Eva; Bassett, Anne; Frisch, Amos; Weizman, Abraham; Gothelf, Doron; Niarchou, Maria; van den Bree, Marianne; Owen, Michael J; Su�er, Damian Heine; Andreo, Jordi Rosell; Armando, Marco; Vicari, Stefano; Digilio, Maria Cristina; Auton, Adam; Kates, Wendy R; Wang, Tao; Shprintzen, Robert J; Emanuel, Beverly S; Morrow, Bernice E.
In:
American Journal of Human Genetics, Vol. 92, No. 3, 07.03.2013, p. 439-47.
Research output: Contribution to journal › Journal article › Research › peer-review
Harvard
Delio, M, Guo, T, McDonald-McGinn, DM, Zackai, E, Herman, S, Kaminetzky, M, Higgins, AM, Coleman, K, Chow, C, Jalbrzikowski, M, Jarlbrzkowski, 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, Su�er, DH, Andreo, JR, Armando, M, Vicari, S, Digilio, MC, Auton, A, Kates, WR, Wang, T, Shprintzen, RJ, Emanuel, BS & Morrow, BE 2013, '
Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes',
American Journal of Human Genetics, vol. 92, no. 3, pp. 439-47.
https://doi.org/10.1016/j.ajhg.2013.01.018APA
Delio, M., Guo, T., McDonald-McGinn, D. M., Zackai, E., Herman, S., Kaminetzky, M., Higgins, A. M., Coleman, K., Chow, C., Jalbrzikowski, M., Jarlbrzkowski, M., Bearden, C. E., Bailey, A., Vangkilde, A., Olsen, L., Olesen, C., Skovby, F.
, Werge, T. M., Templin, L., ... Morrow, B. E. (2013).
Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes.
American Journal of Human Genetics,
92(3), 439-47.
https://doi.org/10.1016/j.ajhg.2013.01.018Vancouver
Delio M, Guo T, McDonald-McGinn DM, Zackai E, Herman S, Kaminetzky M et al.
Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes.
American Journal of Human Genetics. 2013 Mar 7;92(3):439-47.
https://doi.org/10.1016/j.ajhg.2013.01.018Author
Delio, Maria ; Guo, Tingwei ; McDonald-McGinn, Donna M ; Zackai, Elaine ; Herman, Sean ; Kaminetzky, Mark ; Higgins, Anne Marie ; Coleman, Karlene ; Chow, Carolyn ; Jalbrzikowski, Maria ; Jarlbrzkowski, Maria ; Bearden, Carrie E ; Bailey, Alice ; Vangkilde, Anders ; Olsen, Line ; Olesen, Charlotte ; Skovby, Flemming ; Werge, Thomas M ; Templin, Ludivine ; Busa, Tiffany ; Philip, Nicole ; Swillen, Ann ; Vermeesch, Joris R ; Devriendt, Koen ; Schneider, Maude ; Dahoun, Sophie ; Eliez, Stephan ; Schoch, Kelly ; Hooper, Stephen R ; Shashi, Vandana ; Samanich, Joy ; Marion, Robert ; van Amelsvoort, Therese ; Boot, Erik ; Klaassen, Petra ; Duijff, Sasja N ; Vorstman, Jacob ; Yuen, Tracy ; Silversides, Candice ; Chow, Eva ; Bassett, Anne ; Frisch, Amos ; Weizman, Abraham ; Gothelf, Doron ; Niarchou, Maria ; van den Bree, Marianne ; Owen, Michael J ; Su�er, Damian Heine ; Andreo, Jordi Rosell ; Armando, Marco ; Vicari, Stefano ; Digilio, Maria Cristina ; Auton, Adam ; Kates, Wendy R ; Wang, Tao ; Shprintzen, Robert J ; Emanuel, Beverly S ; Morrow, Bernice E. / Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes. In: American Journal of Human Genetics. 2013 ; Vol. 92, No. 3. pp. 439-47.
Bibtex
@article{cb3d552c3bf14f37980015a5914e5d92,
title = "Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes",
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 Maria Jarlbrzkowski 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�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 = mar,
day = "7",
doi = "10.1016/j.ajhg.2013.01.018",
language = "English",
volume = "92",
pages = "439--47",
journal = "American Journal of Human Genetics",
issn = "0002-9297",
publisher = "Cell Press",
number = "3",
}
RIS
TY - JOUR
T1 - Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes
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 - Jarlbrzkowski, 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 - Su�er, 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 - 2013/3/7
Y1 - 2013/3/7
U2 - 10.1016/j.ajhg.2013.01.018
DO - 10.1016/j.ajhg.2013.01.018
M3 - Journal article
C2 - 23453669
VL - 92
SP - 439
EP - 447
JO - American Journal of Human Genetics
JF - American Journal of Human Genetics
SN - 0002-9297
IS - 3
ER -
