(Q41889623)
Statements
1 reference
Achalasia microcephaly syndrome in a patient with consanguineous parents: support for a.m. being a distinct autosomal recessive condition (English)
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Hernández A
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Reynoso MC
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Soto F
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Quiñones D
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Nazará Z
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Fragoso R
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1 December 1989
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36
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6
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456-458
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Identifiers
1 reference