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One or more keywords matched the following items that are connected to
Youngs, Erin
| Item Type | Name |
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Concept
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Chromosome Aberrations
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Concept
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Chromosome Deletion
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Concept
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Chromosomes, Human, Pair 14
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Concept
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Chromosomes, Human, Pair 15
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Concept
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Chromosomes, Human, Pair 16
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Concept
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Chromosomes, Human, Pair 4
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Concept
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Chromosomes, Human, Pair 9
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Concept
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Chromosome Disorders
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Academic Article
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ANKRD11 gene deletion in a 17-year-old male.
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Academic Article
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An 18-year follow-up report on an infant with a duplication of 9q34.
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Academic Article
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Structural Chromosome Abnormalities Associated with Obesity: Report of Four New subjects and Review of Literature.
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Academic Article
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12-year-old boy with a 4q35.2 microdeletion and involvement of MTNR1A, FAT1, and F11 genes.
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Academic Article
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14q32 deletion syndrome: a clinical report.
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Academic Article
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A clinical report and further delineation of the 14q32 deletion syndrome.
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Academic Article
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Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay.
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