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Hematology Volume 22, 2017 - Issue 8
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Lymphoma

GATA2 null mutation associated with incomplete penetrance in a family with Emberger syndrome

Aniel Jessica Leticia Brambila-TapiaDepartamento de Psicología Básica, Centro Universitario de Ciencias de la Salud (CUCS), Universidad de Guadalajara, Guadalajara, Jalisco, MéxicoCorrespondence[email protected]
ORCID Iconhttp://orcid.org/0000-0002-6455-3662View further author information
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José Elías García-OrtizDivisión de Genética, Centro de Investigación Biomédica de Occidente (CIBO), Instituto Mexicano del Seguro Social (IMSS), Guadalajara, Jalisco, MéxicoORCID Iconhttp://orcid.org/0000-0003-1504-1457View further author information
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Pascal BrouillardHuman Molecular Genetics, de Duve Institute, Université catholique de Louvain, Brussels, BelgiumORCID Iconhttp://orcid.org/0000-0001-9548-8229View further author information
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Ha-Long NguyenHuman Molecular Genetics, de Duve Institute, Université catholique de Louvain, Brussels, BelgiumORCID Iconhttp://orcid.org/0000-0002-4976-1615View further author information
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Miikka VikkulaHuman Molecular Genetics, de Duve Institute, Université catholique de Louvain, Brussels, Belgium;Walloon Excellence in Life sciences and Biotechnology (WELBIO), Université catholique de Louvain, Brussels, BelgiumORCID Iconhttp://orcid.org/0000-0002-6236-338XView further author information
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Blanca Estela Ríos-GonzálezUnidad Médico Familiar #34, Instituto Mexicano del Seguro Social (IMSS), Guadalajara, Jalisco, MéxicoORCID Iconhttp://orcid.org/0000-0001-8197-455XView further author information
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Roberto de Jesús Sandoval-MuñizDoctorado en Genética Humana, Centro Universitario de Ciencias de la Salud (CUCS), Universidad de Guadalajara, Guadalajara, Jalisco, MéxicoORCID Iconhttp://orcid.org/0000-0001-7111-1793View further author information
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Ana Karen Sandoval-TalamantesDoctorado en Genética Humana, Centro Universitario de Ciencias de la Salud (CUCS), Universidad de Guadalajara, Guadalajara, Jalisco, MéxicoORCID Iconhttp://orcid.org/0000-0002-2702-5625View further author information
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Lucina Bobadilla-MoralesDoctorado en Genética Humana, Centro Universitario de Ciencias de la Salud (CUCS), Universidad de Guadalajara, Guadalajara, Jalisco, México;Departamento de Biología Molecular y Genómica, Instituto de Genética Humana, Centro Universitario de Ciencias de la Salud (CUCS), Universidad de Guadalajara, Guadalajara, Jalisco, MéxicoORCID Iconhttp://orcid.org/0000-0001-7324-2287View further author information
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Jorge Román Corona-RiveraDoctorado en Genética Humana, Centro Universitario de Ciencias de la Salud (CUCS), Universidad de Guadalajara, Guadalajara, Jalisco, México;Departamento de Biología Molecular y Genómica, Instituto de Genética Humana, Centro Universitario de Ciencias de la Salud (CUCS), Universidad de Guadalajara, Guadalajara, Jalisco, México;Servicio de Genética, División de Pediatría, Hospital Civil de Guadalajara, ‘Dr. Juan I. Menchaca’, Guadalajara, Jalisco, MéxicoORCID Iconhttp://orcid.org/0000-0001-7968-2267View further author information
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Lisette Arnaud-LopezServicio de Genética, División de Pediatría, Hospital Civil de Guadalajara, ‘Dr. Juan I. Menchaca’, Guadalajara, Jalisco, MéxicoCorrespondence[email protected]
ORCID Iconhttp://orcid.org/0000-0002-3681-6365View further author information
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Pages 467-471 | Published online: 08 Mar 2017

References

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