Abstract
Ruvalcaba syndrome is an autosomal dominant disorder in which microcephaly and an unusual facies are associated with shortened bones in the extremities and changes in the spine.
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Reference
Ruvalcaba RHA, Reichert A, Smith DW (1971) A new familial syndrome with osseous dysplasia and mental deficiency. J Pediatr 79: 450–455
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© 1997 Springer-Verlag London Limited
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Beighton, P., Beighton, G. (1997). Ruvalcaba, R.H.A.. In: The Person Behind the Syndrome. Springer, London. https://doi.org/10.1007/978-1-4471-0925-9_157
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DOI: https://doi.org/10.1007/978-1-4471-0925-9_157
Publisher Name: Springer, London
Print ISBN: 978-1-4471-1236-5
Online ISBN: 978-1-4471-0925-9
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