SIX1 mutation screening in 247 branchio‐oto‐renal syndrome families: a recurrent missense mutation associated with BOR

A Kochhar, DJ Orten, JL Sorensen, SM Fischer… - Human …, 2008 - Wiley Online Library
Branchio‐oto‐renal syndrome (BOR) is a clinically heterogeneous autosomal dominant form
of syndromic hearing loss characterized by variable hearing impairment, malformations of …

SIX1 mutation screening in 247 branchio-oto-renal syndrome families: A recurrent missense mutation associated with BOR

A Kochhar, DJ Orten, JL Sorensen… - Human …, 2008 - experts.nebraska.edu
Branchio-oto-renal syndrome (BOR) is a clinically heterogeneous autosomal dominant form
of syndromic hearing loss characterized by variable hearing impairment, malformations of …

SIX1 mutation screening in 247 branchio-oto-renal syndrome families: a recurrent missense mutation associated with BOR

A Kochhar, DJ Orten, JL Sorensen… - Human …, 2008 - pubmed.ncbi.nlm.nih.gov
Branchio-oto-renal syndrome (BOR) is a clinically heterogeneous autosomal dominant form
of syndromic hearing loss characterized by variable hearing impairment, malformations of …

SIX1 Mutation Screening in 247 Branchio-Oto-Renal Syndrome Families: A Recurrent Missense Mutation Associated With BOR

A Kochhar, DJ Orten, JL Sorensen, SM Fischer… - 2008 - Wiley Online Library
Branchio-oto-renal syndrome (BOR; MIM# 113650) is a clinically heterogeneous autosomal
dominant form of syndromic hearing loss characterized by variable hearing impairment …

[PDF][PDF] SIX1 Mutation Screening in 247 Branchio-Oto-Renal Syndrome Families: A Recurrent Missense Mutation Associated With BOR

A Kochhar, DJ Orten, JL Sorensen, SM Fischer… - 2008 - academia.edu
Branchio-oto-renal syndrome (BOR; MIM# 113650) is a clinically heterogeneous autosomal
dominant form of syndromic hearing loss characterized by variable hearing impairment …

[引用][C] SIX1 mutation screening in 247 branchio-oto-renal syndrome families: a recurrent missense mutation associated with BOR.

A Kochhar, DJ Orten, JL Sorensen, SM Fischer… - 2008 - repository.ubn.ru.nl
Branchio-oto-renal syndrome (BOR) is a clinically heterogeneous autosomal dominant form
of syndromic hearing loss characterized by variable hearing impairment, malformations of …

SIX1 mutation screening in 247 branchio-oto-renal syndrome families: a recurrent missense mutation associated with BOR

A Kochhar, DJ Orten, JL Sorensen, SM Fischer… - Human …, 2008 - iro.uiowa.edu
Branchio-oto-renal syndrome (BOR) is a clinically heterogeneous autosomal dominant form
of syndromic hearing loss characterized by variable hearing impairment, malformations of …

SIX1 mutation screening in 247 branchio-oto-renal syndrome families: a recurrent missense mutation associated with BOR.

A Kochhar, DJ Orten, JL Sorensen, SM Fischer… - Human …, 2008 - europepmc.org
Branchio-oto-renal syndrome (BOR) is a clinically heterogeneous autosomal dominant form
of syndromic hearing loss characterized by variable hearing impairment, malformations of …

SIX1 mutation screening in 247 branchio-oto-renal syndrome families: A recurrent missense mutation associated with BOR

A Kochhar, DJ Orten, JL Sorensen… - Human …, 2008 - providence.elsevierpure.com
Branchio-oto-renal syndrome (BOR) is a clinically heterogeneous autosomal dominant form
of syndromic hearing loss characterized by variable hearing impairment, malformations of …

[引用][C] SIX1mutation screening in 247 branchio-oto-renal syndrome families: a recurrent missense mutation associated with BOR

A Kochhar, DJ Orten, JL Sorensen, SM Fischer… - Human Mutation, 2008 - cir.nii.ac.jp
<i>SIX1</i>mutation screening in 247 branchio-oto-renal syndrome families: a recurrent
missense mutation associated with BOR | CiNii Research CiNii 国立情報学研究所 学術情報 …