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Pamela J Reitnauer

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Pediatric Blood & Cancer|November 18, 2004
Positive association between congenital anomalies and risk of neuroblastomaFlorence Menegaux, Andrew F Olshan, Pamela J Reitnauer, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 8, 2011
Autoimmune polyendocrinopathy associated with ring chromosome 18Nina Jain, Pamela J Reitnauer, Kathleen W Rao, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2010
Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesityRuxandra Bachmann-Gagescu, Heather C Mefford, Charles Cowan, et al.
Cell Reports|August 11, 2015
Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex NeuropathyClaudia Gonzaga-Jauregui, Tamar Harel, Tomasz Gambin, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Pediatric Blood & Cancer|November 18, 2004
Positive association between congenital anomalies and risk of neuroblastomaFlorence Menegaux, Andrew F Olshan, Pamela J Reitnauer, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 8, 2011
Autoimmune polyendocrinopathy associated with ring chromosome 18Nina Jain, Pamela J Reitnauer, Kathleen W Rao, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2010
Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesityRuxandra Bachmann-Gagescu, Heather C Mefford, Charles Cowan, et al.
Cell Reports|August 11, 2015
Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex NeuropathyClaudia Gonzaga-Jauregui, Tamar Harel, Tomasz Gambin, et al.
Pageof 1