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Mulibrey nanism
Clinical Utility Gene Card For: 3-M Syndrome – Update 2013
Patient Advocacy Organizations, Industry Funding, and Conflicts of Interest
Trim37-Deficient Mice Recapitulate Several Features of the Multi-Organ
Repercussions of Inborn Errors of Immunity on Growth☆ Jornal De Pediatria, Vol
2021 Western Medical Research Conference
Constrictive Pericarditis and Primary Amenorrhea with Syndactyly in an Iranian Female: Mulibrey Nanism Syndrome
MECHANISMS in ENDOCRINOLOGY: Novel Genetic Causes of Short Stature
Ccr Pediatric Oncology Series
Review and Hypothesis: Syndromes with Severe Intrauterine Growth
Gynecological Tumors in Mulibrey Nanism and Role for RING Finger Protein TRIM37 in the Pathogenesis of Ovarian Fibrothecomas
Delineating Phenotypes of Rare Disease
Mulibrey Nanism: Clinical Features and Diagnostic Criteria N Karlberg, H Jalanko, J Perheentupa, M Lipsanen-Nyman
Trimming Down to TRIM37: Relevance to Inflammation, Cardiovascular Disorders, and Cancer in MULIBREY Nanism
Syndromes and Constitutional Chromosomal Abnormalities
DFNA49, a Novel Locus for Autosomal Dominant Non- Syndromic Hearing
ETR Ped Endocrinology ESPE Approved 24April2021 FINAL
CCR PEDIATRIC ONCOLOGY SERIES CCR Pediatric Oncology Series Pediatric Cancer Predisposition and Surveillance: an Overview, and a Tribute to Alfred G
Curriculum Vitae: Chad S. Weldy, MD, Ph.D
Top View
Procedural Document: Rare Disease Nomenclature in English
Constrictive Pericarditis in a 19-Month-Old Child
Genetic Syndromes Associated with Immune Abnormalities
Renal Findings in Patients with Mulibrey Nanism
Save the Date for 2022 WMRC January 20-22, 2022
Anaesthesia for the Dysmorphic Child DEFINITIONS
Mulibrey Nanism. Characterization of Hypogonadism, Infertility and Tumors
Meckel Syndrome: Genetics, Perinatal Findings, and Differential Diagnosis
Ventriculomegaly Precision Panel Overview Indications Clinical Utility
HHS Public Access Author Manuscript
Medical Text Indexer (MTI)
Type 1 Established Condition List
Pericardial Constriction in 28-Year-Old Patient with Mulibrey Nanism
Molecular Etiology Disclosed by Array CGH in Patients with Silver–Russell Syndrome Or Similar Phenotypes
Mulibrey Nanism Maria Piccione, Emanuela Salzano Department of Sciences for Health Promotion and Mother and Child Care G
Prevalence and Incidence of Rare Diseases
MULIBREY NANISM Clinical Characteristics and Pathophysiologic Features of Growth Restriction, Insulin Resistance and Tumour Development