No abstract available
MeSH terms
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Abnormalities, Multiple / genetics*
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Child
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Congenital Abnormalities / genetics*
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Female
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Genetic Diseases, Inborn* / genetics
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Hamartoma Syndrome, Multiple / diagnosis
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Hamartoma Syndrome, Multiple / genetics
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Humans
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Infant, Newborn
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Loeys-Dietz Syndrome / diagnosis
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Loeys-Dietz Syndrome / genetics
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Male
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Receptor, Transforming Growth Factor-beta Type II / genetics
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Syndrome
Substances
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Receptor, Transforming Growth Factor-beta Type II
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TGFBR2 protein, human