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Síndrome de discapacidad intelectual ligada a X con macrocefalia por deleción del gen BRWD3
by
Arroyo Carrera, Ignacio
,
Romero Peguero, Rafael
,
Martín Fernández, Rebeca
,
Ramajo Polo, Alba
,
García Navas Núñez, Verónica Deyanira
Published in
Revista de neurologiá
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Síndrome de rotura de Varsovia: una causa de microcefalia congénita y sordera neurosensorial
by
Arroyo Carrera, Ignacio
,
Solo de Zaldívar Tristancho, María
,
García-Navas Núñez, Verónica Deyanira
,
Ramajo Polo, Alba
,
Gutiérrez Agujetas, Marta
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Revista de neurologiá
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X-linked intellectual disability syndrome with macrocephaly due to BRWD3 gene deletion
by
Arroyo-Carrera, I
,
Romero-Peguero, R
,
Martín-Fernández, R
,
Ramajo-Polo, A
,
García-Navas Núñez, V
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Revista de neurologiá
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Warsaw breakage syndrome: an etiology for congenital microcephaly and sensorineural deafness
by
Arroyo-Carrera, I
,
Solo de Zaldívar-Tristancho, M
,
García Navas-Núñez, V D
,
Ramajo-Polo, A
,
Gutiérrez-Agujetas, M
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Revista de neurologiá
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Síndrome de discapacidad intelectual ligada a X con macrocefalia por deleción del gen BRWD3
by
Arroyo-Carrera, Ignacio
,
Romero-Peguero, Rafael
,
Martín-Fernández, Rebeca
,
Ramajo-Polo, Alba
,
Núñez, Verónica García-Navas
Published in
Revista de neurologiá
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Síndrome de rotura de Varsovia: una causa de microcefalia congénita y sordera neurosensorial
by
Arroyo-Carrera, Ignacio
,
Solo de Zaldívar-Tristancho, María
,
García Navas-Núñez, Verónica D.
,
Ramajo-Polo, Alba
,
Gutiérrez-Agujetas, Marta
Published in
Revista de neurologiá
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Abnormalities, Multiple - Genetics
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Bromodomain Containing Proteins
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Brwd3 Gene
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Child
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Chromosome Breakage Syndromes
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Cochlear Anomalies
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Cohesinopathies
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Ddx11
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Dead-Box Rna Helicases - Genetics
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Deafness
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Gene Deletion
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Ezb Electronic Journals Library
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