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The Gene for Pendred Syndrome Is Located between D7S501 and D7S692 in a 1.7-cM Region on Chromosome 7q

Data up to Jan 2025

Published1997
Citations25
References24

Total Citations Per Year

Abstract

References (24)

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Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification

1996 • 161 citations

Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4

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Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population

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Pendred's Syndrome

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THE CONCENTRATION OF PEROXIDASE IN NORMAL AND ADENOMATOUS HUMAN THYROID TISSUE WITH SPECIAL REFERENCE TO PATIENTS WITH PENDRED'S SYNDROME

1973 • 22 citations

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