Genetics and phenomics of Pendred syndrome
A Bizhanova, P Kopp - Molecular and cellular endocrinology, 2010 - Elsevier
Pendred syndrome is an autosomal recessive disorder characterized by sensorineural
deafness, goiter and a partial defect in iodide organification. Goiter development and …
deafness, goiter and a partial defect in iodide organification. Goiter development and …
Genetics and phenomics of Pendred syndrome.
A Bizhanova, P Kopp - 2010 - cabidigitallibrary.org
Pendred syndrome is an autosomal recessive disorder characterized by sensorineural
deafness, goiter and a partial defect in iodide organification. Goiter development and …
deafness, goiter and a partial defect in iodide organification. Goiter development and …
Genetics and phenomics of Pendred syndrome
A Bizhanova, P Kopp - Molecular and Cellular Endocrinology, 2010 - hero.epa.gov
Pendred syndrome is an autosomal recessive disorder characterized by sensorineural
deafness, goiter and a partial defect in iodide organification. Goiter development and …
deafness, goiter and a partial defect in iodide organification. Goiter development and …
[引用][C] Genetics and phenomics of Pendred syndrome
A Bizhanova, P Kopp - Molecular and Cellular Endocrinology, 2010 - cir.nii.ac.jp
Genetics and phenomics of Pendred syndrome
A Bizhanova, PA Kopp - Molecular and Cellular …, 2010 - scholars.northwestern.edu
Pendred syndrome is an autosomal recessive disorder characterized by sensorineural
deafness, goiter and a partial defect in iodide organification. Goiter development and …
deafness, goiter and a partial defect in iodide organification. Goiter development and …
Genetics and phenomics of Pendred syndrome
A Bizhanova, P Kopp - Molecular and cellular …, 2010 - pubmed.ncbi.nlm.nih.gov
Pendred syndrome is an autosomal recessive disorder characterized by sensorineural
deafness, goiter and a partial defect in iodide organification. Goiter development and …
deafness, goiter and a partial defect in iodide organification. Goiter development and …
Genetics and phenomics of Pendred syndrome.
A Bizhanova, P Kopp - Molecular and Cellular Endocrinology, 2010 - europepmc.org
Pendred syndrome is an autosomal recessive disorder characterized by sensorineural
deafness, goiter and a partial defect in iodide organification. Goiter development and …
deafness, goiter and a partial defect in iodide organification. Goiter development and …
Genetics and phenomics of Pendred syndrome
A Bizhanova, P Kopp - Molecular and Cellular Endocrinology, 2010 - infona.pl
Pendred syndrome is an autosomal recessive disorder characterized by sensorineural
deafness, goiter and a partial defect in iodide organification. Goiter development and …
deafness, goiter and a partial defect in iodide organification. Goiter development and …
Genetics and phenomics of Pendred syndrome
A Bizhanova, P Kopp - Molecular and Cellular Endocrinology, 2010 - infona.pl
Pendred syndrome is an autosomal recessive disorder characterized by sensorineural
deafness, goiter and a partial defect in iodide organification. Goiter development and …
deafness, goiter and a partial defect in iodide organification. Goiter development and …