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Achalasia microcephaly syndrome in a patient with consanguineous parents: support for a.m. being a distinct autosomal recessive condition

✍ Scribed by Alejandro Hernández; Martha Celina Reynoso; Fernando Soto; David Quiñones; Zamira Nazará; Ruben Fragoso


Book ID
115089981
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
254 KB
Volume
36
Category
Article
ISSN
0009-9163

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