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Search Results - HUDAC, L. D
Search Results - HUDAC, L. D
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Sterically Hindered Reactions of Grignard Reagents with Schiff Bases
by
EMLING, BERTIN L
,
HORVATH, R. J
,
SARACENO, A. J
,
ELLERMEYER, E. F
,
HAILE, L
,
HUDAC, L. D
Published in
Journal of organic chemistry
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Developmental trajectories for young children with 16p11.2 copy number variation
by
Bernier, Raphael
,
Hudac, Caitlin M.
,
Chen, Qixuan
,
Zeng, Chubing
,
Wallace, Arianne Stevens
,
Gerdts, Jennifer
,
Earl, Rachel
,
Peterson, Jessica
,
Wolken, Anne
,
Peters, Alana
,
Hanson, Ellen
,
Goin‐Kochel, Robin P.
,
Kanne, Stephen
,
Snyder, LeeAnne Green
,
Chung, Wendy K.
Published in
American journal of medical genetics. Part B, Neuropsychiatric genetics
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Longitudinal report of child with de novo 16p11.2 triplication
by
Wallace, Arianne S.
,
Hudac, Caitlin M.
,
Steinman, Kyle J.
,
Peterson, Jessica L.
,
DesChamps, Trent D.
,
Duyzend, Michael H.
,
Nuttle, Xander
,
Eichler, Evan E.
,
Bernier, Raphael A.
Published in
Clinical case reports
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Neural mechanisms underlying neurooptometric rehabilitation following traumatic brain injury
by
Hudac, Caitlin M
,
Kota, Srinivas
,
Nedrow, James L
,
Molfese, Dennis L
Published in
Eye and brain
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Longitudinal report of child with de novo 16p11.2 triplication
by
Wallace, Arianne S
,
Hudac, Caitlin M
,
Steinman, Kyle J
,
Peterson, Jessica L
,
DesChamps, Trent D
,
Duyzend, Michael H
,
Nuttle, Xander
,
Eichler, Evan E
,
Bernier, Raphael A
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Clinical case reports
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American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics
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Journal Of Organic Chemistry
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16P11.2 Deletion
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16P11.2 Duplication
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16P11.2 Triplication
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Asd Risk Variant
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Autism Spectrum Disorder
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Chromosomes, Human, Pair 16 - Genetics
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Copy Number Variation
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