![Neutropenia, Severe Congenital, 8, Autosomal Dominant disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials Neutropenia, Severe Congenital, 8, Autosomal Dominant disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials](http://malacards.blob.core.windows.net/network-images-v5-15-2/neutropenia_severe_congenital_8_autosomal_dominant_related_diseases.jpg)
Neutropenia, Severe Congenital, 8, Autosomal Dominant disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
![SciELO - Brasil - Shwachman-Diamond syndrome: first molecular diagnosis in a Brazilian child Shwachman-Diamond syndrome: first molecular diagnosis in a Brazilian child SciELO - Brasil - Shwachman-Diamond syndrome: first molecular diagnosis in a Brazilian child Shwachman-Diamond syndrome: first molecular diagnosis in a Brazilian child](https://minio.scielo.br/documentstore/1806-0870/7xXP6yKKR75cwRmp4Z46FdS/9273f3baabafbd7abd4c491dbc1bfed4f0aed8cf.jpg)
SciELO - Brasil - Shwachman-Diamond syndrome: first molecular diagnosis in a Brazilian child Shwachman-Diamond syndrome: first molecular diagnosis in a Brazilian child
![PDF] Deconstructing Niche Contributions to Leukemogenesis: Modeling Shwachman-Diamond Syndrome | Semantic Scholar PDF] Deconstructing Niche Contributions to Leukemogenesis: Modeling Shwachman-Diamond Syndrome | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/8b2026b50fbb37bfb503baf1617e86a54cc8a4a1/157-Table2-1.png)
PDF] Deconstructing Niche Contributions to Leukemogenesis: Modeling Shwachman-Diamond Syndrome | Semantic Scholar
![Shwachman‒Diamond syndrome with initial features mimicking common variable immunodeficiency - Pediatrics & Neonatology Shwachman‒Diamond syndrome with initial features mimicking common variable immunodeficiency - Pediatrics & Neonatology](https://www.pediatr-neonatol.com/cms/asset/e28a9e14-04fa-43b5-91ae-21e850511814/gr1.jpg)
Shwachman‒Diamond syndrome with initial features mimicking common variable immunodeficiency - Pediatrics & Neonatology
![Inflammatory manifestations in patients with Shwachman–Diamond syndrome: A novel phenotype - Furutani - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library Inflammatory manifestations in patients with Shwachman–Diamond syndrome: A novel phenotype - Furutani - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/f9a79278-8dc7-4cf3-983b-bdb45ed4a857/ajmga61593-fig-0001-m.jpg)
Inflammatory manifestations in patients with Shwachman–Diamond syndrome: A novel phenotype - Furutani - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
![Shwachman Diamond syndrome: narrow genotypic spectrum and variable clinical features | Pediatric Research Shwachman Diamond syndrome: narrow genotypic spectrum and variable clinical features | Pediatric Research](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41390-022-02009-8/MediaObjects/41390_2022_2009_Fig1_HTML.png)