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Author/Creator Lebel, Robert Roger

1. Expanding the molecular spectrum and the neurological phenotype related to CAMTA1 variants. Issue 2 (23rd November 2020)

Authors:
Jacobs, Eva Z.; Brown, Kathleen; Byler, Melissa C.; D'haenens, Erika; Dheedene, Annelies; Henderson, Lindsay B.; Humberson, Jennifer B.; van Jaarsveld, Richard H.; Kanani, Farah; Lebel, Robert Roger; Millan, Francisca; Oegema, Renske; Oostra, Ann; Parker, Michael J.; Rhodes, Lindsay; Saenz, Marga...
Journal:
Clinical genetics
Issue:
Volume 99:Issue 2(2021)
Page Start:
259
Record Type:
Journal Article
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5. Two cases of Legg–Perthes and intellectual disability in Tricho–Rhino–Phalangeal syndrome type 1 associated with novel TRPS1 mutations. Issue 6 (3rd March 2017)

Authors:
Gilman, Jordana L.; Newman, Heather A.; Freeman, Rebecca; Singh, Kathryn E.; Puckett, Rebecca L.; Morohashi, David K.; Stein, Constance; Palomino, Kathryn; Lebel, Robert Roger; Kimonis, Virginia E.
Journal:
American journal of medical genetics
Issue:
Volume 173:Issue 6(2017)
Page Start:
1663
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗