![TOWNES-BROCKS SYNDROME: REPORT OF THREE ADDITIONAL PATIENTS WITH PREVIOUSLY UNDESCRIBED RENAL AND CARDIAC ABNORMALITIES. - Abstract - Europe PMC TOWNES-BROCKS SYNDROME: REPORT OF THREE ADDITIONAL PATIENTS WITH PREVIOUSLY UNDESCRIBED RENAL AND CARDIAC ABNORMALITIES. - Abstract - Europe PMC](https://europepmc.org/articles/PMC5295470/bin/nihms813014f2.jpg)
TOWNES-BROCKS SYNDROME: REPORT OF THREE ADDITIONAL PATIENTS WITH PREVIOUSLY UNDESCRIBED RENAL AND CARDIAC ABNORMALITIES. - Abstract - Europe PMC
![Townes–Brocks syndrome – airway management conditions improve with age: report of follow up of a single case - Umesh - 2009 - Pediatric Anesthesia - Wiley Online Library Townes–Brocks syndrome – airway management conditions improve with age: report of follow up of a single case - Umesh - 2009 - Pediatric Anesthesia - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/3ee398e5-9a54-4f17-9733-47714c0db48a/pan_2901_f1.jpg)
Townes–Brocks syndrome – airway management conditions improve with age: report of follow up of a single case - Umesh - 2009 - Pediatric Anesthesia - Wiley Online Library
![Delayed diagnosis of Townes‑Brocks syndrome with multicystic kidneys and renal failure caused by a novel SALL1 nonsense mutation: A case report Delayed diagnosis of Townes‑Brocks syndrome with multicystic kidneys and renal failure caused by a novel SALL1 nonsense mutation: A case report](https://www.spandidos-publications.com/article_images/etm/11/4/etm-11-04-1249-g00.jpg)
Delayed diagnosis of Townes‑Brocks syndrome with multicystic kidneys and renal failure caused by a novel SALL1 nonsense mutation: A case report
![Implications for genotype–phenotype predictions in Townes–Brocks syndrome: Case report of a novel SALL1 deletion and review of the literature - Miller - 2012 - American Journal of Medical Genetics Part A - Implications for genotype–phenotype predictions in Townes–Brocks syndrome: Case report of a novel SALL1 deletion and review of the literature - Miller - 2012 - American Journal of Medical Genetics Part A -](https://onlinelibrary.wiley.com/cms/asset/369e4347-215f-46ae-9fb4-14aac3665770/mfig001.jpg)
Implications for genotype–phenotype predictions in Townes–Brocks syndrome: Case report of a novel SALL1 deletion and review of the literature - Miller - 2012 - American Journal of Medical Genetics Part A -
![HUWE1 mutations in Juberg-Marsidi and Brooks syndromes: the results of an X-chromosome exome sequencing study | BMJ Open HUWE1 mutations in Juberg-Marsidi and Brooks syndromes: the results of an X-chromosome exome sequencing study | BMJ Open](https://bmjopen.bmj.com/content/bmjopen/6/4/e009537/F1.large.jpg)
HUWE1 mutations in Juberg-Marsidi and Brooks syndromes: the results of an X-chromosome exome sequencing study | BMJ Open
![Don't read this book by my mother, she's crazy: Living with Asperger's Syndrome (also as I'm not broken, I'm just different & Wings to fly) : Brooks, Linda Ruth, Attwood, Tony: Amazon.de: Don't read this book by my mother, she's crazy: Living with Asperger's Syndrome (also as I'm not broken, I'm just different & Wings to fly) : Brooks, Linda Ruth, Attwood, Tony: Amazon.de:](https://m.media-amazon.com/images/I/61LkXPoDcbL._AC_UF1000,1000_QL80_.jpg)
Don't read this book by my mother, she's crazy: Living with Asperger's Syndrome (also as I'm not broken, I'm just different & Wings to fly) : Brooks, Linda Ruth, Attwood, Tony: Amazon.de:
![PDF] Variable expression observed in a Korean family with Townes-Brocks syndrome caused by a SALL1 mutation | Semantic Scholar PDF] Variable expression observed in a Korean family with Townes-Brocks syndrome caused by a SALL1 mutation | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/c91085d10541264c40e88e099081e8246fb930e9/3-Figure2-1.png)
PDF] Variable expression observed in a Korean family with Townes-Brocks syndrome caused by a SALL1 mutation | Semantic Scholar
![Whole-exome sequencing identified a novel heterozygous mutation of SALL1 and a new homozygous mutation of PTPRQ in a Chinese family with Townes-Brocks syndrome and hearing loss | BMC Medical Genomics | Full Whole-exome sequencing identified a novel heterozygous mutation of SALL1 and a new homozygous mutation of PTPRQ in a Chinese family with Townes-Brocks syndrome and hearing loss | BMC Medical Genomics | Full](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs12920-021-00871-9/MediaObjects/12920_2021_871_Fig1_HTML.png)
Whole-exome sequencing identified a novel heterozygous mutation of SALL1 and a new homozygous mutation of PTPRQ in a Chinese family with Townes-Brocks syndrome and hearing loss | BMC Medical Genomics | Full
![PDF] Delayed diagnosis of Townes-Brocks syndrome with multicystic kidneys and renal failure caused by a novel SALL1 nonsense mutation: A case report | Semantic Scholar PDF] Delayed diagnosis of Townes-Brocks syndrome with multicystic kidneys and renal failure caused by a novel SALL1 nonsense mutation: A case report | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/a075e929be996d86fee122cb58e1239c007742d0/2-Figure1-1.png)