Opening book details…
About this book
IRF2BPL Is Associated with Neurological Phenotypes by Paul C. Marcogliese & Vandana Shashi & Rebecca C. Spillmann & Nicholas Stong & Jill A. Rosenfeld & Mary Kay Koenig & Julián A. Martínez-Agosto & Matthew Herzog & Agnes H. Chen & Patricia I. Dickson & Henry J. Lin & Moin U. Vera & Noriko Salamon & John... is a book available to read on EtoBox.
- Author
- Paul C. Marcogliese & Vandana Shashi & Rebecca C. Spillmann & Nicholas Stong & Jill A. Rosenfeld & Mary Kay Koenig & Julián A. Martínez-Agosto & Matthew Herzog & Agnes H. Chen & Patricia I. Dickson & Henry J. Lin & Moin U. Vera & Noriko Salamon & John...
- Publisher
- Elsevier
- Published
- 2018
- Language
- EN
More by Paul C. Marcogliese & Vandana Shashi & Rebecca C. Spillmann & Nicholas Stong & Jill A. Rosenfeld & Mary Kay Koenig & Julián A. Martínez-Agosto & Matthew Herzog & Agnes H. Chen & Patricia I. Dickson & Henry J. Lin & Moin U. Vera & Noriko Salamon & John...
Similar books
- Characterizing the Causal Pathway for Genetic Variants Associated with Neurological Phenotypes Using Human Brain-Derived Proteome Data — Nelson K. Kibinge & Caroline L. Relton & Tom R. Gaunt & Tom G. Richardson (2020)
- NFIB Haploinsufficiency Is Associated with Intellectual Disability and Macrocephaly — Ina Schanze & Jens Bunt & Jonathan W.C. Lim & Denny Schanze & Ryan J. Dean & Marielle Alders & Patricia Blanchet & Tania Attié-Bitach & Siren Berland & Steven Boogert & Sangamitra Boppudi & Caitlin J. Bridges & Megan T. Cho & William B. Dobyns & Dian... (2018)
- BICRA, a SWI/SNF Complex Member, Is Associated with BAF-Disorder Related Phenotypes in Humans and Model Organisms — Scott Barish & Tahsin Stefan Barakat & Brittany C. Michel & Nazar Mashtalir & Jennifer B. Phillips & Alfredo M. Valencia & Berrak Ugur & Jeremy Wegner & Tiana M. Scott & Brett Bostwick & David R. Murdock & Hongzheng Dai & Elena Perenthaler & Anita... (2020)
- Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features — Peter D. Turnpenny & Michael J. Wright & Melissa Sloman & Richard Caswell & Anthony J. van Essen & Erica Gerkes & Rolph Pfundt & Susan M. White & Nava Shaul-Lotan & Lori Carpenter & G. Bradley Schaefer & Alan Fryer & A. Micheil Innes & Kirsten P....
- Loss of Oxidation Resistance 1, OXR1, Is Associated with an Autosomal-Recessive Neurological Disease with Cerebellar Atrophy and Lysosomal Dysfunction — Julia Wang & Justine Rousseau & Emily Kim & Sophie Ehresmann & Yi-Ting Cheng & Lita Duraine & Zhongyuan Zuo & Ye-Jin Park & David Li-Kroeger & Weimin Bi & Lee-Jun Wong & Jill Rosenfeld & Joseph Gleeson & Eissa Faqeih & Fowzan S. Alkuraya & Klaas J.... (2019)
- Bi-allelic Variants in INTS11 Are Associated with a Complex Neurological Disorder — Burak Tepe & Erica L. Macke & Marcello Niceta & Monika Weisz Hubshman & Oguz Kanca & Laura Schultz-Rogers & Yuri A. Zarate & G. Bradley Schaefer & Jorge Luis Granadillo De Luque & Daniel J. Wegner & Benjamin Cogne & Brigitte Gilbert-Dussardier & Xavier... (2023)