De novo microdeletion ofBCL11Ais associated with severe speech sound disorder

A patient with de novo 0.45 Mb deletion of 2p16.1: The role ofBCL11A,PAPOLG,REL, andFLJ16341in the 2p15-p16.1 microdeletion syndrome

(2013) Miroslava Hancarova et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

An Erythroid Enhancer of BCL11A Subject to Genetic Variation Determines Fetal Hemoglobin Level

(2013) D. E. Bauer et al.   SCIENCE

Deficits in sequential processing manifest in motor and linguistic tasks in a multigenerational family with childhood apraxia of speech

(2013) Beate Peter et al.   CLINICAL LINGUISTICS & PHONETICS

Associations among measures of sequential processing in motor and linguistics tasks in adults with and without a family history of childhood apraxia of speech: A replication study

(2013) Le Button et al.   CLINICAL LINGUISTICS & PHONETICS

Interstitial deletion of chromosome 2p15-16.1: Report of two patients and critical review of current genotype–phenotype correlation

(2012) Maria Piccione et al.   European Journal of Medical Genetics

Novel candidate genes and regions for childhood apraxia of speech identified by array comparative genomic hybridization

(2012) Jennifer J.S. Laffin et al.   GENETICS IN MEDICINE

Motor sequencing deficit as an endophenotype of speech sound disorder

(2012) Beate Peter et al.   PSYCHIATRIC GENETICS

Deletion 2p15-16.1 syndrome: Case report and review

(2011) Paolo Prontera et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Further characterization of microdeletion syndrome involving 2p15-p16.1

(2010) Têmis Maria Félix et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Transcriptional silencing of fetal hemoglobin by BCL11A

(2010) Vijay G. Sankaran et al.   Annals of the New York Academy of Sciences

A newly recognised microdeletion syndrome of 2p15-16.1 manifesting moderate developmental delay, autistic behaviour, short stature, microcephaly, and dysmorphic features: a new patient with 3.2 Mb deletion

(2009) J-S Liang et al.   JOURNAL OF MEDICAL GENETICS

Bcl11A/CTIP1 regulates expression of DCC and MAP1b in control of axon branching and dendrite outgrowth

(2009) Ting-Yu Kuo et al.   MOLECULAR AND CELLULAR NEUROSCIENCE

Confirmation of dyslexia susceptibility loci on chromosomes 1p and 2p, but not 6p in a Dutch sib-pair collection

(2007) Carolien G.F. de Kovel et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS