Robert J. Shprintzen, Ph.D., Series Editor

This series will include volumes covering both general and specific topics related to genetic disease, including areas related to speech, language, hearing, cognition, education, behavior, and interdisciplinary care. The authors and editors in this series have been selected from a range of professions, affording the series a multidisciplinary approach to genetic syndromes that emphasizes the translation of modern science to state-of-the-art care.

Books featured in this series

Educating Children with Velo-Cardio-Facial Syndrome, 22q11.2 Deletion Syndrome, and DiGeorge Syndrome

Third Edition

Donna Cutler-Landsman

Details: 387 pages, B&W, Softcover, 7" x 10"

ISBN13: 978-1-63550-167-4

© 2020 | Available

Educating Children with Velo-Cardio-Facial Syndrome (also Known as 22q11.2 Deletion Syndrome and DiGeorge Syndrome)

Second Edition

Donna Cutler-Landsman

Details: 328 pages, B&W, Softcover, 7" x 10"

ISBN13: 978-1-59756-492-2

© 2013 | Available

Velo-Cardio-Facial Syndrome, Volume II: Treatment of Communication Disorders

First Edition

Karen J. Golding-Kushner, Robert J. Shprintzen

Details: 256 pages, B&W, Softcover + DVD, 7" x 10"

ISBN13: 978-1-59756-157-0

© 2011 | Available

Velo-Cardio-Facial Syndrome, Volume I

First Edition

Robert J. Shprintzen, Karen J. Golding-Kushner

Details: 289 pages, B&W, Softcover, 7" x 10"

ISBN13: 978-1-59756-071-9

© 2008 | Available

Waardenburg Syndrome

First Edition

Alice Kahn

Details: 136 pages, Full Color, Softcover, 7" x 10"

ISBN13: 978-1-59756-021-4

© 2007 | Available