Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals.

Solomon BD, Lacbawan F, Mercier S, Clegg NJ, Delgado MR, Rosenbaum K, Dubourg C, David V, Olney AH, Wehner LE, Hehr U, Bale S, Paulussen A, Smeets HJ, Hardisty E, Tylki-Szymanska A, Pronicka E, Clemens M, McPherson E, Hennekam RC, Hahn J, Stashinko E, Levey E, Wieczorek D, Roeder E, Schell-Apacik CC, Booth CW, Thomas RL, Kenwrick S, Cummings DA, Bous SM, Keaton A, Balog JZ, Hadley D, Zhou N, Long R, Vélez JI, Pineda-Alvarez DE, Odent S, Roessler E, Muenke M

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DOI: 10.1136/jmg.2009.073049
Published: 2010 Aug
Container: Journal of medical genetics
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1136/jmg.2009.073049,
  title = {Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals.},
  author = {Solomon BD and Lacbawan F and Mercier S and Clegg NJ and Delgado MR and Rosenbaum K and Dubourg C and David V and Olney AH and Wehner LE and Hehr U and Bale S and Paulussen A and Smeets HJ and Hardisty E and Tylki-Szymanska A and Pronicka E and Clemens M and McPherson E and Hennekam RC and Hahn J and Stashinko E and Levey E and Wieczorek D and Roeder E and Schell-Apacik CC and Booth CW and Thomas RL and Kenwrick S and Cummings DA and Bous SM and Keaton A and Balog JZ and Hadley D and Zhou N and Long R and Vélez JI and Pineda-Alvarez DE and Odent S and Roessler E and Muenke M},
  year = {2010},
  journal = {Journal of medical genetics},
  doi = {10.1136/jmg.2009.073049},
  url = {https://doi.org/10.1136/jmg.2009.073049}
}

RIS

TY  - JOUR
TI  - Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals.
AU  - Solomon BD
AU  - Lacbawan F
AU  - Mercier S
AU  - Clegg NJ
AU  - Delgado MR
AU  - Rosenbaum K
AU  - Dubourg C
AU  - David V
AU  - Olney AH
AU  - Wehner LE
AU  - Hehr U
AU  - Bale S
AU  - Paulussen A
AU  - Smeets HJ
AU  - Hardisty E
AU  - Tylki-Szymanska A
AU  - Pronicka E
AU  - Clemens M
AU  - McPherson E
AU  - Hennekam RC
AU  - Hahn J
AU  - Stashinko E
AU  - Levey E
AU  - Wieczorek D
AU  - Roeder E
AU  - Schell-Apacik CC
AU  - Booth CW
AU  - Thomas RL
AU  - Kenwrick S
AU  - Cummings DA
AU  - Bous SM
AU  - Keaton A
AU  - Balog JZ
AU  - Hadley D
AU  - Zhou N
AU  - Long R
AU  - Vélez JI
AU  - Pineda-Alvarez DE
AU  - Odent S
AU  - Roessler E
AU  - Muenke M
PY  - 2010
JO  - Journal of medical genetics
DO  - 10.1136/jmg.2009.073049
UR  - https://doi.org/10.1136/jmg.2009.073049
ER  -

APA

BD, S., F, L., S, M., NJ, C., MR, D., K, R., C, D., V, D., AH, O., LE, W., U, H., S, B., A, P., HJ, S., E, H., A, T., E, P., M, C., E, M., RC, H., J, H., E, S., E, L., D, W., E, R., CC, S., CW, B., RL, T., S, K., DA, C., SM, B., A, K., JZ, B., D, H., N, Z., R, L., JI, V., DE, P., S, O., E, R., & M, M. (2010). Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals.. Journal of medical genetics. https://doi.org/10.1136/jmg.2009.073049

Source records

pubmed · retrieved 2026-09-26T10:56:44.821Z