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Linda P Manwaring

Showing results (1-10 of 5) with videos related to

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RN|August 30, 2008
Lysosomal storage diseasesLinda P Manwaring, Patricia A Jamerson, Rachel Slaugh
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|April 2, 2011
A novel missense mutation in the MEN1 gene in a patient with multiple endocrine neoplasia type 1Runhua Hou, Linda P Manwaring, Jeffrey F Moley, et al.
Pediatric Radiology|October 11, 2008
Diffusion-weighted and dynamic contrast-enhanced imaging as markers of clinical behavior in children with optic pathway gliomaSarah C Jost, Joseph W Ackerman, Joel R Garbow, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 19, 2014
Fabry disease in infancy and early childhood: a systematic literature reviewDawn A Laney, Dawn S Peck, Andrea M Atherton, et al.
Journal of Medical Genetics|October 11, 2011
Int22h-1/int22h-2-mediated Xq28 rearrangements: intellectual disability associated with duplications and in utero male lethality with deletionsAyman W El-Hattab, Ping Fang, Weihong Jin, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
RN|August 30, 2008
Lysosomal storage diseasesLinda P Manwaring, Patricia A Jamerson, Rachel Slaugh
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|April 2, 2011
A novel missense mutation in the MEN1 gene in a patient with multiple endocrine neoplasia type 1Runhua Hou, Linda P Manwaring, Jeffrey F Moley, et al.
Pediatric Radiology|October 11, 2008
Diffusion-weighted and dynamic contrast-enhanced imaging as markers of clinical behavior in children with optic pathway gliomaSarah C Jost, Joseph W Ackerman, Joel R Garbow, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 19, 2014
Fabry disease in infancy and early childhood: a systematic literature reviewDawn A Laney, Dawn S Peck, Andrea M Atherton, et al.
Journal of Medical Genetics|October 11, 2011
Int22h-1/int22h-2-mediated Xq28 rearrangements: intellectual disability associated with duplications and in utero male lethality with deletionsAyman W El-Hattab, Ping Fang, Weihong Jin, et al.
Pageof 1