Add to ORKGhumans causes hypoparathyroidism, sensorineural deafness and renal dysplasia (HDR) syndrome (Bilous et al., 1992; Van Esch et al., 2000), which displays a high degree of phenotypic heterogeneity. Man
textabstractHuman HDR (hypoparathyroidism, deafness and renal dysplasia)-syndrome is caused by haplo...
Abstract Background Hypoparathyroidism, sensorineural hearing loss, and renal disease (HDR) syndrome...
Context: The hypoparathyroidism, deafness, renal dysplasia (HDR) syndrome is caused by mutations in ...
Hypoparathyroidism, sensorineural deafness and renal dysplasia (HDR) syndrome (MIM 146255) is a rare...
Terminal deletions of chromosome 10p result in a DiGeorge-like phenotype that includes hypoparathyro...
The hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome is an autosomal dominant disorder cau...
The hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome is an autosomal dominant disorder cau...
Abstract HDR syndrome is a rare autosomal dominant disorder caused by mutations in the GATA3 gene an...
We report on GATA3 analysis and the phenotypic spectrum in nine Japanese families with the HDR syndr...
Hypoparathyroidism, sensorineural deafness, and renal dysgenesis syndrome is an autosomal dominant d...
Hypoparathyroidism, sensorineural deafness, and renal dysgenesis syndrome with a GATA3 mutation Case...
Background: Hypoparathyroidism-deafness-renal dysplasia (HDR) syndrome is an autosomal dominant diso...
The hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome is an autosomal dominant disord...
The hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome is an autosomal dominant disord...
Abstract Autosomal dominant hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome are typ...
textabstractHuman HDR (hypoparathyroidism, deafness and renal dysplasia)-syndrome is caused by haplo...
Abstract Background Hypoparathyroidism, sensorineural hearing loss, and renal disease (HDR) syndrome...
Context: The hypoparathyroidism, deafness, renal dysplasia (HDR) syndrome is caused by mutations in ...
Hypoparathyroidism, sensorineural deafness and renal dysplasia (HDR) syndrome (MIM 146255) is a rare...
Terminal deletions of chromosome 10p result in a DiGeorge-like phenotype that includes hypoparathyro...
The hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome is an autosomal dominant disorder cau...
The hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome is an autosomal dominant disorder cau...
Abstract HDR syndrome is a rare autosomal dominant disorder caused by mutations in the GATA3 gene an...
We report on GATA3 analysis and the phenotypic spectrum in nine Japanese families with the HDR syndr...
Hypoparathyroidism, sensorineural deafness, and renal dysgenesis syndrome is an autosomal dominant d...
Hypoparathyroidism, sensorineural deafness, and renal dysgenesis syndrome with a GATA3 mutation Case...
Background: Hypoparathyroidism-deafness-renal dysplasia (HDR) syndrome is an autosomal dominant diso...
The hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome is an autosomal dominant disord...
The hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome is an autosomal dominant disord...
Abstract Autosomal dominant hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome are typ...
textabstractHuman HDR (hypoparathyroidism, deafness and renal dysplasia)-syndrome is caused by haplo...
Abstract Background Hypoparathyroidism, sensorineural hearing loss, and renal disease (HDR) syndrome...
Context: The hypoparathyroidism, deafness, renal dysplasia (HDR) syndrome is caused by mutations in ...