Author: "Scelsa S" / Topic: hypogonadotropic hypogonadism - Searchworks@Jio Institute Digital Library Search Results

Searchworks

Select search scope, currently: Articles

Catalog

books, media & more in Jio Institute collections

Articles

journal articles & other e-resources

Your search keyword '"Scelsa S"' showing total 1 results

Start Over Author "Scelsa S" Topic hypogonadotropic hypogonadism

1 results on '"Scelsa S"'

1. Compound heterozygous PNPLA6 mutations cause Boucher–Neuhäuser syndrome with late-onset ataxia

Author: Deik, A., Johannes, B., Rucker, J. C., Sánchez, E., Brodie, S. E., Deegan, E., Landy, K., Kajiwara, Y., Scelsa, S., Saunders-Pullman, R., and Paisán-Ruiz, C.
Published: 2014
Full Text: View/download PDF

Catalog

Books, media, physical & digital resources

See catalog results