Array analysis and molecular studies of INI1 in an infant with deletion 22q13 (Phelan-McDermid Syndrome) and atypical teratoid/rhabdoid tumor

Shyam Sathyamoorthi; Jaime Morales; Jose Bermudez; Lori McBride; Mark Luquette; Robin McGoey; Nora Oates; Stephen Hales; Jaclyn A. Biegel; Yves Lacassie

doi:10.1002/ajmg.a.32775

Array analysis and molecular studies of INI1 in an infant with deletion 22q13 (Phelan-McDermid Syndrome) and atypical teratoid/rhabdoid tumor

Shyam Sathyamoorthi, Jaime Morales, Jose Bermudez, Lori McBride, Mark Luquette, Robin McGoey, Nora Oates, Stephen Hales, Jaclyn A. Biegel, Yves Lacassie

Laboratory Medicine and Pathology

Research output: Contribution to journal › Letter › peer-review

15 Scopus citations

Original language	English (US)
Pages (from-to)	1067-1069
Number of pages	3
Journal	American Journal of Medical Genetics, Part A
Volume	149
Issue number	5
DOIs	https://doi.org/10.1002/ajmg.a.32775
State	Published - May 2009

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Sathyamoorthi, S., Morales, J., Bermudez, J., McBride, L., Luquette, M., McGoey, R., Oates, N., Hales, S., Biegel, J. A., & Lacassie, Y. (2009). Array analysis and molecular studies of INI1 in an infant with deletion 22q13 (Phelan-McDermid Syndrome) and atypical teratoid/rhabdoid tumor. American Journal of Medical Genetics, Part A, 149(5), 1067-1069. https://doi.org/10.1002/ajmg.a.32775

Sathyamoorthi, S, Morales, J, Bermudez, J, McBride, L, Luquette, M, McGoey, R, Oates, N, Hales, S, Biegel, JA & Lacassie, Y 2009, 'Array analysis and molecular studies of INI1 in an infant with deletion 22q13 (Phelan-McDermid Syndrome) and atypical teratoid/rhabdoid tumor', American Journal of Medical Genetics, Part A, vol. 149, no. 5, pp. 1067-1069. https://doi.org/10.1002/ajmg.a.32775

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Array analysis and molecular studies of INI1 in an infant with deletion 22q13 (Phelan-McDermid Syndrome) and atypical teratoid/rhabdoid tumor

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