Search Results (13)
Click the Why column to see why an item matched the search.
| Match | Type | Why |
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| 1.39 Mb inherited interstitial deletion in 12p13.33 associated with developmental delay. | Academic Article |
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| A 9-month-old baby with subdural hematomas, retinal hemorrhages, and developmental delay. | Academic Article |
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| De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation. | Academic Article |
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| Deletion of ERF and CIC causes abnormal skull morphology and global developmental delay. | Academic Article |
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| De novo frameshift mutation in ASXL3 in a patient with global developmental delay, microcephaly, and craniofacial anomalies. | Academic Article |
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| Report of a patient with developmental delay, hearing loss, growth retardation, and cleft lip and palate and a deletion of 7q34-36.1: review of distal 7q deletions. | Academic Article |
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| Soden, Sarah | Person |
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| Lane, Robert | Person |
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| Park, Taeju | Person |
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| Abdelmoity, Ahmed | Person |
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| Farrow, Emily | Person |
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| Rush, Eric | Person |
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| Cohen, Ana | Person |
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