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Search Results - Elizondo-Cárdenas, Gabriela
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A novel interstitial deletion of 2q22.3 q23.3 in a patient with dysmorphic features, epilepsy, aganglionosis, pure red cell aplasia, and skeletal malformations
by
Bravo-Oro, Antonio
,
Lurie, Iosif W.
,
Elizondo-Cárdenas, Gabriela
,
Peña-Zepeda, Claudia
,
Salazar-Martínez, Abel
,
Correa-González, Cecilia
,
Castrillo, José Luis
,
Avila, Silvia
,
Esmer, Carmen
Published in
American journal of medical genetics. Part A
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American Journal Of Medical Genetics. Part A
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Subjects
2Q22.3 Q23.3 Deletion
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Aplastic Anemia
1 results
1
Array-Comparative Genomic Hybridization
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1
Array‐Comparative Genomic Hybridization
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1
Bone And Bones - Abnormalities
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1
Brachydactyly A1
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Chromosome Deletion
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Chromosomes, Human, Pair 2
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Comparative Genomic Hybridization
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Epilepsy - Genetics
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Genetics & Heredity
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Hirschsprung Disease
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Humans
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Infant, Newborn
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Life Sciences & Biomedicine
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Male
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Red-Cell Aplasia, Pure - Genetics
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Science & Technology
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Wiley-Blackwell Journals
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Wiley
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