Five new TTF1/NKX2.1 mutations in brain-lung-thyroid syndrome: rescue by PAX8 synergism in one case

Mutation of a Gene for Thyroid Transcription Factor-1 (TITF1) in a Patient with Clinical Features of Resistance to Thyrotropin

(2008) Keisuke NAGASAKI et al.   ENDOCRINE JOURNAL

Deletion ofPAX9and oligodontia: a third family and review of the literature

(2008) ANDREA GUALA et al.   International Journal of Paediatric Dentistry

Lethal Respiratory Failure and Mild Primary Hypothyroidism in a Term Girl with ade NovoHeterozygous Mutation in theTITF1/NKX2.1Gene

(2008) Emilie Maquet et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Psychosis, short stature in benign hereditary chorea: A novel thyroid transcription factor-1 mutation

(2008) Amir Glik et al.   MOVEMENT DISORDERS

Postmitotic Nkx2-1 Controls the Migration of Telencephalic Interneurons by Direct Repression of Guidance Receptors

(2008) Sandrina Nóbrega-Pereira et al.   NEURON

Genomic profiling identifies TITF1 as a lineage-specific oncogene amplified in lung cancer

(2008) K A Kwei et al.   ONCOGENE

A Novel NKX2.1 Mutation in a Family with Hypothyroidism and Benign Hereditary Chorea

(2008) Alfonso Massimiliano Ferrara et al.   THYROID

Functional characterization of a novel mutation in TITF-1 in a patient with benign hereditary chorea

(2007) Claudia Provenzano et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES