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Microcephalic osteodysplastic primordial dwarfism type I with biallelic  mutations in the RNU4ATAC gene. - Abstract - Europe PMC
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
Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II - ScienceDirect

A Novel PCNT Frame Shift Variant (c.7511delA) Causing Osteodysplastic  Primordial Dwarfism of Majewski Type 2 (MOPD II) | Semantic Scholar
A Novel PCNT Frame Shift Variant (c.7511delA) Causing Osteodysplastic Primordial Dwarfism of Majewski Type 2 (MOPD II) | Semantic Scholar

Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe  anemia and MRI brain findings of MOPD type II | Semantic Scholar
Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II | Semantic Scholar

Microcephalic osteodysplastic primordial dwarfism type 1 | BMJ Case Reports
Microcephalic osteodysplastic primordial dwarfism type 1 | BMJ Case Reports

Primordial Dwarfism: Life Expectancy, Pictures, Symptoms, Types, More
Primordial Dwarfism: Life Expectancy, Pictures, Symptoms, Types, More

Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe  anemia and MRI brain findings of MOPD type II - ScienceDirect
Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II - ScienceDirect

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 – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on CyberLeninka open science

Genetics for the pediatric endocrinologists – 2 Primordial short stature in  children and adolescents - Journal of Pediatric Endocrinology and Diabetes
Genetics for the pediatric endocrinologists – 2 Primordial short stature in children and adolescents - Journal of Pediatric Endocrinology and Diabetes

Phenotypic traits of patients with microcephalic osteodysplastic... |  Download Scientific Diagram
Phenotypic traits of patients with microcephalic osteodysplastic... | Download Scientific Diagram

PDF) Striking Hematological Abnormalities in Patients With Microcephalic  Osteodysplastic Primordial Dwarfism Type II (MOPD II): A Potential Role of  Pericentrin in Hematopoiesis
PDF) Striking Hematological Abnormalities in Patients With Microcephalic Osteodysplastic Primordial Dwarfism Type II (MOPD II): A Potential Role of Pericentrin in Hematopoiesis

Identification of RNU4ATAC mutations in MOPD I patients. (A)... | Download  Scientific Diagram
Identification of RNU4ATAC mutations in MOPD I patients. (A)... | Download Scientific Diagram

Primordial Dwarfism: A Case Series From North East of Iran and Literature  Review - Journal of Pediatrics Review
Primordial Dwarfism: A Case Series From North East of Iran and Literature Review - Journal of Pediatrics Review

Binding activity of the 15.5K protein to the 5 ′ stem–loop of MOPD I... |  Download Scientific Diagram
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 type I with biallelic mutations in the RNU4ATAC gene. - Abstract - Europe PMC

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

Case Report Clinical Findings and Dental Manifestations Associated With  Microcephalic Osteodysplastic Primordial Dwarfism Type I
Case Report Clinical Findings and Dental Manifestations Associated With Microcephalic Osteodysplastic Primordial Dwarfism Type I

Frontiers | A Novel PCNT Frame Shift Variant (c.7511delA) Causing  Osteodysplastic Primordial Dwarfism of Majewski Type 2 (MOPD II)
Frontiers | A Novel PCNT Frame Shift Variant (c.7511delA) Causing Osteodysplastic Primordial Dwarfism of Majewski Type 2 (MOPD II)

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
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

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  lissencephaly and brain cyst - ScienceDirect
Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with lissencephaly and brain cyst - 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
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

IJMS | Free Full-Text | Whole-Exome and Transcriptome Sequencing Expands  the Genotype of Majewski Osteodysplastic Primordial Dwarfism Type II
IJMS | Free Full-Text | Whole-Exome and Transcriptome Sequencing Expands the Genotype of Majewski Osteodysplastic Primordial Dwarfism Type II

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
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

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
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

Characteristic features of MOPDII. a Patient 1. A 7-week-old female... |  Download Scientific Diagram
Characteristic features of MOPDII. a Patient 1. A 7-week-old female... | Download Scientific Diagram

Effect of recombinant insulin-like growth factor-1 treatment on short-term  linear growth in a child with Majewski osteodysplastic primordial dwarfism  type II and hepatic insufficiency
Effect of recombinant insulin-like growth factor-1 treatment on short-term linear growth in a child with Majewski osteodysplastic primordial dwarfism type II and hepatic insufficiency