GENETIC SYNDROMES AND COMMUNICATION DISORDERS
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
Details: 387 pages, B&W, Softcover, 7" x 10"
© 2020 | Available
Educating Children with Velo-Cardio-Facial Syndrome (also Known as 22q11.2 Deletion Syndrome and DiGeorge Syndrome)
Details: 328 pages, B&W, Softcover, 7" x 10"
© 2013 | Available
Karen J. Golding-Kushner, Robert J. Shprintzen
Details: 256 pages, B&W, Softcover + DVD, 7" x 10"
© 2011 | Available
Robert J. Shprintzen, Karen J. Golding-Kushner
Details: 289 pages, B&W, Softcover, 7" x 10"
© 2008 | Available