No abstract available
MeSH terms
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Cerebral Cortex / abnormalities*
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Cerebral Cortex / pathology
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Chromosomes, Human, Pair 15 / genetics
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Female
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Humans
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Imaging, Three-Dimensional
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Infant, Newborn
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Magnetic Resonance Imaging
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Nervous System Malformations / complications*
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Nervous System Malformations / diagnosis*
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Prader-Willi Syndrome / complications*
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Prader-Willi Syndrome / diagnosis*
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Prader-Willi Syndrome / genetics
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Sequence Deletion