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GATAD2B-associated neurodevelopmental disorder (GAND): clin..:

Shieh, Christine ; Jones, Natasha ; Vanle, Brigitte...
qt7683d0mf. , 2020

Link: https://escholarship.org/uc/item/7683d0mf

RT Journal
T1 <Title>GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt7683d0mf&Exemplar=1&LAN=DE
				
A1 Shieh, Christine
A1 Jones, Natasha
A1 Vanle, Brigitte
A1 Au, Margaret
A1 Huang, Alden Y
A1 Silva, Ana PG
A1 Lee, Hane
A1 Douine, Emilie D
A1 Otero, Maria G
A1 Choi, Andrew
A1 Grand, Katheryn
A1 Taff, Ingrid P
A1 Delgado, Mauricio R
A1 Hajianpour, MJ
A1 Seeley, Andrea
A1 Rohena, Luis
A1 Vernon, Hilary
A1 Gripp, Karen W
A1 Vergano, Samantha A
A1 Mahida, Sonal
A1 Naidu, Sakkubai
A1 Sousa, Ana Berta
A1 Wain, Karen E
A1 Challman, Thomas D
A1 Beek, Geoffrey
A1 Basel, Donald
A1 Ranells, Judith
A1 Smith, Rosemarie
A1 Yusupov, Roman
A1 Freckmann, Mary-Louise
A1 Ohden, Lisa
A1 Davis-Keppen, Laura
A1 Chitayat, David
A1 Dowling, James J
A1 Finkel, Richard
A1 Dauber, Andrew
A1 Spillmann, Rebecca
A1 Pena, Loren DM
A1 Metcalfe, Kay
A1 Splitt, Miranda
A1 Lachlan, Katherine
A1 McKee, Shane A
A1 Hurst, Jane
A1 Fitzpatrick, David R
A1 Morton, Jenny EV
A1 Cox, Helen
A1 Venkateswaran, Sunita
A1 Young, Juan I
A1 Marsh, Eric D
A1 Nelson, Stanley F
A1 Martinez, Julian A
A1 Graham, John M
A1 Kini, Usha
A1 Mackay, Joel P
A1 Pierson, Tyler Mark
PB eScholarship, University of California
YR 2020
K1 Genetics
K1 Clinical Research
K1 Congenital Structural Anomalies
K1 Brain Disorders
K1 Pediatric
K1 Intellectual and Developmental Disabilities (IDD)
K1 2.1 Biological and endogenous factors
K1 Aetiology
K1 Child
K1 Female
K1 GATA Transcription Factors
K1 Humans
K1 Intellectual Disability
K1 Megalencephaly
K1 Neurodevelopmental Disorders
K1 Nucleosomes
K1 Phenotype
K1 Pregnancy
K1 Repressor Proteins
K1 GATAD2B
K1 NuRD complex
K1 apraxia of speech
K1 chromatin remodeling
K1 macrocephaly
K1 Undiagnosed Diseases Network
K1 Clinical Sciences
K1 Genetics & Heredity
JF qt7683d0mf
LK http://dx.doi.org/https://escholarship.org/uc/item/7683d0mf
DO https://escholarship.org/uc/item/7683d0mf
SF ELIB - SuUB Bremen

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