Microcephalic osteodysplastic primordial dwarfism type 1 | BMJ Case Reports
Genes | Free Full-Text | Modifier Genes in Microcephaly: A Report on WDR62, CEP63, RAD50 and PCNT Variants Exacerbating Disease Caused by Biallelic Mutations of ASPM and CENPJ
A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder - Abdel‐Salam - 2011 - American Journal of Medical Genetics Part
Genetics for the pediatric endocrinologists – 2 Primordial short stature in children and adolescents - Journal of Pediatric Endocrinology and Diabetes
Figure 1 from Majewski osteodysplastic primordial dwarfism type II: clinical findings and dental management of a child patient | Semantic Scholar
Binding activity of the 15.5K protein to the 5 ′ stem–loop of MOPD I... | Download Scientific Diagram
Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC gene. - Abstract - Europe PMC
Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II - ScienceDirect
Primordial Dwarfism: Life Expectancy, Pictures, Symptoms, Types, More
Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with lissencephaly and brain cyst – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on CyberLeninka open science
Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with lissencephaly and brain cyst - ScienceDirect
Case Report Clinical Findings and Dental Manifestations Associated With Microcephalic Osteodysplastic Primordial Dwarfism Type I
PDF) Striking Hematological Abnormalities in Patients With Microcephalic Osteodysplastic Primordial Dwarfism Type II (MOPD II): A Potential Role of Pericentrin in Hematopoiesis
Microcephalic osteodysplastic primordial dwarfism type 1 | BMJ Case Reports
Rational Design of Potent Peptide Inhibitors of the PD-1:PD-L1 Interaction for Cancer Immunotherapy | Journal of the American Chemical Society
Rational Design of Potent Peptide Inhibitors of the PD-1:PD-L1 Interaction for Cancer Immunotherapy | Journal of the American Chemical Society
Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II | Semantic Scholar
A novel homozygous mutation of the PCNT gene in a Chinese patient with microcephalic osteodysplastic primordial dwarfism type II - Liu - 2021 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Frontiers | A Novel PCNT Frame Shift Variant (c.7511delA) Causing Osteodysplastic Primordial Dwarfism of Majewski Type 2 (MOPD II)
Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II - ScienceDirect
A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder - Abdel‐Salam - 2011 - American Journal of Medical Genetics Part
Identification of RNU4ATAC mutations in MOPD I patients. (A)... | Download Scientific Diagram
Frontiers | A Novel PCNT Frame Shift Variant (c.7511delA) Causing Osteodysplastic Primordial Dwarfism of Majewski Type 2 (MOPD II)
Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II - ScienceDirect
