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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

Shwachman-Diamond syndrome: MedlinePlus Genetics
Shwachman-Diamond syndrome: MedlinePlus Genetics

Fanconi anemia - Wikiwand
Fanconi anemia - Wikiwand

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

Shwachman-Diamond syndrome: MedlinePlus Genetics
Shwachman-Diamond syndrome: MedlinePlus Genetics

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

group_4_presentation_2_-aplastic_anemia - Wiki
group_4_presentation_2_-aplastic_anemia - Wiki

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

Shwachman-Diamond syndrome: MedlinePlus Genetics
Shwachman-Diamond syndrome: MedlinePlus Genetics

SHWACHMAN-DIAMOND SYNDROME Clinical , Genetic and Radiological Study | Semantic Scholar
SHWACHMAN-DIAMOND SYNDROME Clinical , Genetic and Radiological Study | 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

Shwachman-Bodian-Diamond-Syndrom – Wikipedia
Shwachman-Bodian-Diamond-Syndrom – Wikipedia

Bone Marrow (Human Anatomy): Image, Function, Diseases, and Treatments
Bone Marrow (Human Anatomy): Image, Function, Diseases, and Treatments

Childhood Acute Lymphoblastic Leukemia: Diagnosis, Management, and Complications
Childhood Acute Lymphoblastic Leukemia: Diagnosis, Management, and Complications

group_4_presentation_2_-aplastic_anemia - Wiki
group_4_presentation_2_-aplastic_anemia - Wiki

Exocrine pancreatic insufficiency - Wikipedia
Exocrine pancreatic insufficiency - Wikipedia

group_4_presentation_2_-aplastic_anemia - Wiki
group_4_presentation_2_-aplastic_anemia - Wiki

Fanconi anemia - Wikiwand
Fanconi anemia - Wikiwand

Pathology Outlines - Shwachman-Diamond syndrome
Pathology Outlines - Shwachman-Diamond syndrome

Shwachman-Diamond syndrome: MedlinePlus Genetics
Shwachman-Diamond syndrome: MedlinePlus Genetics

Shwachman-Diamond syndrome: MedlinePlus Genetics
Shwachman-Diamond syndrome: MedlinePlus Genetics

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

Mutations in EFL1, an SBDS partner, are associated with infantile pancytopenia, exocrine pancreatic insufficiency and skeletal anomalies in aShwachman-Diamond like syndrome | Journal of Medical Genetics
Mutations in EFL1, an SBDS partner, are associated with infantile pancytopenia, exocrine pancreatic insufficiency and skeletal anomalies in aShwachman-Diamond like syndrome | Journal of Medical Genetics