![Radiographs of patient 1 at age 5 years: lateral spine (A), pelvis (B),... | Download Scientific Diagram Radiographs of patient 1 at age 5 years: lateral spine (A), pelvis (B),... | Download Scientific Diagram](https://www.researchgate.net/publication/51382529/figure/fig2/AS:601743079522318@1520478138307/Radiographs-of-patient-1-at-age-5-years-lateral-spine-A-pelvis-B-knee-C-and-hand.png)
Radiographs of patient 1 at age 5 years: lateral spine (A), pelvis (B),... | Download Scientific Diagram
![214 - Toby Brown & Jesse Hohn of Colorado Are Two Dads Who Each Have Children With Shwachman-Diamond Syndrome - 21st Century Dads 214 - Toby Brown & Jesse Hohn of Colorado Are Two Dads Who Each Have Children With Shwachman-Diamond Syndrome - 21st Century Dads](https://i0.wp.com/21stcenturydads.org/wp-content/uploads/2022/08/214.jpg?fit=720%2C720&ssl=1)
214 - Toby Brown & Jesse Hohn of Colorado Are Two Dads Who Each Have Children With Shwachman-Diamond Syndrome - 21st Century Dads
Bone marrow failure and developmental delay caused by mutations in poly(A)-specific ribonuclease (PARN)
![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)
Shwachman Diamond syndrome: narrow genotypic spectrum and variable clinical features | Pediatric Research
![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
![The Shwachman–Bodian–Diamond syndrome gene mutations cause a neonatal form of spondylometaphysial dysplasia (SMD) resembling SMD Sedaghatian type | Journal of Medical Genetics The Shwachman–Bodian–Diamond syndrome gene mutations cause a neonatal form of spondylometaphysial dysplasia (SMD) resembling SMD Sedaghatian type | Journal of Medical Genetics](https://jmg.bmj.com/content/jmedgenet/44/4/e73/F1.large.jpg)
The Shwachman–Bodian–Diamond syndrome gene mutations cause a neonatal form of spondylometaphysial dysplasia (SMD) resembling SMD Sedaghatian type | Journal of Medical Genetics
![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
![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
![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)