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Laron syndrome
Repercussions of Inborn Errors of Immunity on Growth☆ Jornal De Pediatria, Vol
Prevalence and Incidence of Rare Diseases: Bibliographic Data
MECHANISMS in ENDOCRINOLOGY: Novel Genetic Causes of Short Stature
Update on New GH-IGF Axis Genetic Defects
Genetic Disorder
Laron Syndrome
Blueprint Genetics Comprehensive Growth Disorders / Skeletal
Test Requisition Form (Dna & Genetic Tests)
E-Chapter 2.P65
Laron Syndrome- a Disorder Associated with a Reduced Risk of Cancer: a Review on the Molecular Aspects
A Case with Laron Syndrome
Genetic Testing Medical Policy – Genetics
Multiple Primary Urological Tumors in a Patient with Proportionate Dwarfism
Long-Term Effects of Recombinant Human Insulin-Like Growth Factor I
Endocrine Test Selection and Interpretation
Prof. Laron's Publications
180K ISCA Array
A Growth Hormone Mol Path: First Published As 10.1136/Mp.54.5.311 on 1 October 2001
Top View
Fourth Joint LWPESJESPE Meeting 1993 Final Program
Growth Curves for Laron Syndrome Arch Dis Child: First Published As 10.1136/Adc.68.6.768 on 1 June 1993
Hormone Resistance Syndromes Series: Contemporary Endocrinology
View the 2019 Index
An Update on Laron Syndrome 345
The Role of Insulin-Like Growth Factor-I in Neuroendocrine Function and the Consequent Effects on Sexual Maturation: Inferences from Animal Models
Growth Hormone Receptor Mutations Related to Individual Dwarfism
Why Are People with Laron Syndrome Immune to Cancer?
Aase–Smith Syndrome, 231 Abboud, M.R., 381 Abdallat Syndrome, 196
On Human Short Stature
Blueprint Genetics Comprehensive Short Stature Syndrome Panel
Genetic Disorders Leading to Hypoglycaemia
Pediatric Endocrinology
Introduction of New Recombinant Insulin-Like Growth Factor-1 – Current and Future Perspectives
Type of the Paper (Article
Low Level IGF-1 and Common Variable Immune Deficiency: an Unusual Combination
Genetic Evaluation of Short Stature Laurie H
Diagnosed Cases of Rare Diseases at CENTOGENE January 2012 to June 2016
Applying Bioinformatic Platforms, in Vitro, and in Vivo Functional Assays
Growth Hormone Insensitivity Syndrome Associated Ith Syringomyelia and Type I Chiari Malformation
Current Perspective on Dominant Negative Mutations: Trends, Scope and Relevance
Transient Juvenile Hypoglycemia in Growth Hormone Receptor Deficiency – Mechanistic Insights from Laron Syndrome and Tailored Animal Models
Growth Hormone in the Aging Male
RING CHROMOSOME 5 in a CHILD with SEVERE GROWTH We Are Currently Investigating the Effect of Biosynthctic Growth Hormone (Rhgh One Year RETARDATION
1. Congenital Urea Cycle Disorders 2. Citrullinemia 3
Primary Growth Hormone Resistance Or Insensitivity): the Personal Experience 1958–2003
Primary GH Insensitivity '(Laron Syndrome) Caused by a Novel 4 Kb
The Globe and Orbit in Laron Syndrome
Phenotypic Characterization of Spontaneously Mutated Rats Showing Lethal Dwarfism and Epilepsy
Prevalence and Incidence of Rare Diseases: Bibliographic Data
2021 Pathology & Lab CPT Updates
Prevalence and Incidence of Rare Diseases
Section Heading Section Sub Pediatric Endocrinology Growth Hormone
Advances in Endocrinology
Meet the Expert HANDOUTS
Role of the GH-IGF1 Axis on the Hypothalamus–Pituitary–Testicular Axis Function: Lessons from Laron Syndrome
Short Stature Precision Panel Overview Indications Clinical Utility
A Mammalian Model for Laron Syndrome Produced by Targeted Disruption of the Mouse Growth Hormone Receptor͞binding Protein Gene (The Laron Mouse)
Primary Growth Hormone Insensitivity
Growth Hormone
Orphanet Report Series Rare Diseases Collection
New Insights from Unbiased Panel and Whole-Exome Sequencing in A
Mendelian Disorders Among Jews
JOHNS HOPKINS ALL CHILDREN's HOSPITAL Molecular Genetics Test Requisition
Recessive Gene List V2.0
Genome-Wide Profiling of Laron Syndrome Patients Identifies Novel