![SMCHD1 is mutated in Bosma arhinia microphthalmia syndrome and isolated... | Download Scientific Diagram SMCHD1 is mutated in Bosma arhinia microphthalmia syndrome and isolated... | Download Scientific Diagram](https://www.researchgate.net/publication/312170544/figure/fig1/AS:613507489878094@1523282992903/SMCHD1-is-mutated-in-Bosma-arhinia-microphthalmia-syndrome-and-isolated-arhinia-a-b.png)
SMCHD1 is mutated in Bosma arhinia microphthalmia syndrome and isolated... | Download Scientific Diagram
![Review of paraneoplastic syndromes associated with oropharyngeal squamous cell carcinoma Mathew DG, Rooban T, Janani V, Joshua E, Rao U K, Ranganathan K - J Oral Maxillofac Pathol Review of paraneoplastic syndromes associated with oropharyngeal squamous cell carcinoma Mathew DG, Rooban T, Janani V, Joshua E, Rao U K, Ranganathan K - J Oral Maxillofac Pathol](https://www.jomfp.in/articles/2010/14/2/images/JOralMaxillofacPathol_2010_14_2_41_72499_f3.jpg)
Review of paraneoplastic syndromes associated with oropharyngeal squamous cell carcinoma Mathew DG, Rooban T, Janani V, Joshua E, Rao U K, Ranganathan K - J Oral Maxillofac Pathol
![IJERPH | Free Full-Text | Storyboarding HIV Infected Young People’s Adherence to Antiretroviral Therapy in Lower- to Upper Middle-Income Countries: A New-Materialist Qualitative Evidence Synthesis | HTML IJERPH | Free Full-Text | Storyboarding HIV Infected Young People’s Adherence to Antiretroviral Therapy in Lower- to Upper Middle-Income Countries: A New-Materialist Qualitative Evidence Synthesis | HTML](https://www.mdpi.com/ijerph/ijerph-19-11317/article_deploy/html/images/ijerph-19-11317-g005.png)
IJERPH | Free Full-Text | Storyboarding HIV Infected Young People’s Adherence to Antiretroviral Therapy in Lower- to Upper Middle-Income Countries: A New-Materialist Qualitative Evidence Synthesis | HTML
![SMCHD1 mutation spectrum for facioscapulohumeral muscular dystrophy type 2 (FSHD2) and Bosma arhinia microphthalmia syndrome (BAMS) reveals disease-specific localisation of variants in the ATPase domain | Journal of Medical Genetics SMCHD1 mutation spectrum for facioscapulohumeral muscular dystrophy type 2 (FSHD2) and Bosma arhinia microphthalmia syndrome (BAMS) reveals disease-specific localisation of variants in the ATPase domain | Journal of Medical Genetics](https://jmg.bmj.com/sites/default/files/highwire/jmedgenet/56/10.cover-source.jpg)
SMCHD1 mutation spectrum for facioscapulohumeral muscular dystrophy type 2 (FSHD2) and Bosma arhinia microphthalmia syndrome (BAMS) reveals disease-specific localisation of variants in the ATPase domain | Journal of Medical Genetics
![Nutrients | Free Full-Text | Wikipedia, Google Trends and Diet: Assessment of Temporal Trends in the Internet Users' Searches in Italy before and during COVID-19 Pandemic Nutrients | Free Full-Text | Wikipedia, Google Trends and Diet: Assessment of Temporal Trends in the Internet Users' Searches in Italy before and during COVID-19 Pandemic](https://pub.mdpi-res.com/nutrients/nutrients-13-03683/article_deploy/html/images/nutrients-13-03683-g002.png?1634736679)
Nutrients | Free Full-Text | Wikipedia, Google Trends and Diet: Assessment of Temporal Trends in the Internet Users' Searches in Italy before and during COVID-19 Pandemic
![Bosma arhinia microphthalmia syndrome: Clinical report and review of the literature - Brasseur - 2016 - American Journal of Medical Genetics Part A - Wiley Online Library Bosma arhinia microphthalmia syndrome: Clinical report and review of the literature - Brasseur - 2016 - American Journal of Medical Genetics Part A - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/83c2b319-8e2d-4344-85fc-2a320e6d56b6/ajmga37572-fig-0003-m.jpg)
Bosma arhinia microphthalmia syndrome: Clinical report and review of the literature - Brasseur - 2016 - American Journal of Medical Genetics Part A - Wiley Online Library
![Molecules | Free Full-Text | Natural Products for the Prevention and Treatment of Hangover and Alcohol Use Disorder Molecules | Free Full-Text | Natural Products for the Prevention and Treatment of Hangover and Alcohol Use Disorder](https://www.mdpi.com/molecules/molecules-21-00064/article_deploy/html/images/molecules-21-00064-g002.png)
Molecules | Free Full-Text | Natural Products for the Prevention and Treatment of Hangover and Alcohol Use Disorder
![Alex Magee's research works | Belfast Health and Social Care Trust, Belfast (BHSCT) and other places Alex Magee's research works | Belfast Health and Social Care Trust, Belfast (BHSCT) and other places](https://www.researchgate.net/profile/Diana-Baralle/publication/267738926/figure/fig1/AS:267698219253830@1440835637719/Figure2-Clinical-photographs-Patient-1-is-shown-at-age-1year-7months-A-and-B-and_Q320.jpg)
Alex Magee's research works | Belfast Health and Social Care Trust, Belfast (BHSCT) and other places
![Facioscapulohumeral Muscular Dystrophy 2, Digenic disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials Facioscapulohumeral Muscular Dystrophy 2, Digenic disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials](https://malacards.blob.core.windows.net/network-images-v5-13-2/facioscapulohumeral_muscular_dystrophy_2_digenic_related_diseases.jpg)
Facioscapulohumeral Muscular Dystrophy 2, Digenic disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
![De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development | Nature Genetics De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development | Nature Genetics](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fng.3765/MediaObjects/41588_2017_Article_BFng3765_Fig3_HTML.jpg)
De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development | Nature Genetics
![SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome | Nature Genetics SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome | Nature Genetics](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fng.3743/MediaObjects/41588_2017_Article_BFng3743_Fig1_HTML.jpg)