Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear
LA Everett, H Morsli, DK Wu… - Proceedings of the …, 1999 - National Acad Sciences
Pendred's syndrome is an autosomal-recessive disorder characterized by deafness and
goiter. After our recent identification of the human gene mutated in Pendred's syndrome …
goiter. After our recent identification of the human gene mutated in Pendred's syndrome …
Expression Pattern of the Mouse Ortholog of the Pendred's Syndrome Gene (Pds) Suggests a Key Role for Pendrin in the Inner Ear
LA Everett, H Morsli, DK Wu… - Proceedings of the …, 1999 - ui.adsabs.harvard.edu
Pendred's syndrome is an autosomal-recessive disorder characterized by deafness and
goiter. After our recent identification of the human gene mutated in Pendred's syndrome …
goiter. After our recent identification of the human gene mutated in Pendred's syndrome …
Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear
LA Everett, H Morsli, DK Wu… - Proceedings of the …, 1999 - pubmed.ncbi.nlm.nih.gov
Pendred's syndrome is an autosomal-recessive disorder characterized by deafness and
goiter. After our recent identification of the human gene mutated in Pendred's syndrome …
goiter. After our recent identification of the human gene mutated in Pendred's syndrome …
[PDF][PDF] Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear
LA EVERETT, H MORSLI, DK WU… - Proc. Natl. Acad. Sci …, 1999 - researchgate.net
Pendred's syndrome is an autosomalrecessive disorder characterized by deafness and
goiter. After our recent identification of the human gene mutated in Pendred's syndrome …
goiter. After our recent identification of the human gene mutated in Pendred's syndrome …
Expression pattern of the mouse ortholog of the Pendred's syndrome gene ( Pds ) suggests a key role for pendrin in the inner ear
LA Everett, H Morsli, DK Wu, ED Green - Proceedings of the National …, 1999 - cir.nii.ac.jp
抄録< jats: p> Pendred's syndrome is an autosomal-recessive disorder characterized by
deafness and goiter. After our recent identification of the human gene mutated in Pendred's …
deafness and goiter. After our recent identification of the human gene mutated in Pendred's …
[HTML][HTML] Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear
LA Everett, H Morsli, DK Wu… - Proceedings of the …, 1999 - ncbi.nlm.nih.gov
Pendred's syndrome is an autosomal-recessive disorder characterized by deafness and
goiter. After our recent identification of the human gene mutated in Pendred's syndrome …
goiter. After our recent identification of the human gene mutated in Pendred's syndrome …
[PDF][PDF] Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear
LA EVERETT, H MORSLI, DK WU… - Proc. Natl. Acad. Sci …, 1999 - academia.edu
Pendred's syndrome is an autosomalrecessive disorder characterized by deafness and
goiter. After our recent identification of the human gene mutated in Pendred's syndrome …
goiter. After our recent identification of the human gene mutated in Pendred's syndrome …
Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear.
LA Everett, H Morsli, DK Wu… - Proceedings of the …, 1999 - europepmc.org
Pendred's syndrome is an autosomal-recessive disorder characterized by deafness and
goiter. After our recent identification of the human gene mutated in Pendred's syndrome …
goiter. After our recent identification of the human gene mutated in Pendred's syndrome …
Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear
LA Everett, H Morsli, DK Wu, ED Green - Proceedings of the National …, 1999 - hero.epa.gov
Pendred's syndrome is an autosomal-recessive disorder characterized by deafness and
goiter. After our recent identification of the human gene mutated in Pendred's syndrome …
goiter. After our recent identification of the human gene mutated in Pendred's syndrome …
Expression Pattern of the Mouse Ortholog of the Pendred's Syndrome Gene (Pds) Suggests a Key Role for Pendrin in the Inner Ear
LA Everett, H Morsli, DK Wu, ED Green - … Academy of Sciences of the United …, 1999 - JSTOR
Pendred's syndrome is an autosomal-recessive disorder characterized by deafness and
goiter. After our recent identification of the human gene mutated in Pendred's syndrome …
goiter. After our recent identification of the human gene mutated in Pendred's syndrome …