Find Research outputs - UTMB Health Research Expert Profiles
Find Research outputs - UTMB Health Research Expert Profiles (researchexperts.utmb.edu)
Reuben Matalon, MD, PhD - Publications - UTMB Health Research Expert Profiles
Reuben Matalon, MD, PhD - Publications - UTMB Health Research Expert Profiles (researchexperts.utmb.edu)
Association of genetic variations in the CSF2 and CSF3 genes with lung function in smoking-induced COPD | European Respiratory...
Association of genetic variations in the CSF2 and CSF3 genes with lung function in smoking-induced COPD | European Respiratory... (erj.ersjournals.com)
Plus it
Plus it (erj.ersjournals.com)
Plus it
Plus it (erj.ersjournals.com)
Newborn Screening Practices and Alpha-Thalassemia Detection - United States, 2016 | MMWR
Newborn Screening Practices and Alpha-Thalassemia Detection - United States, 2016 | MMWR (cdc.gov)
Enhanced dexamethasone resistance in cystic fibrosis cells: potential use for heterozygote detection and prenatal diagnosis |...
Enhanced dexamethasone resistance in cystic fibrosis cells: potential use for heterozygote detection and prenatal diagnosis |... (science.sciencemag.org)
Robbins Pathologic Basis of Disease - Ramzi S. Cotran - Google Books
Robbins Pathologic Basis of Disease - Ramzi S. Cotran - Google Books (books.google.ca)
Research | Fanconi Anemia Research Fund
Research | Fanconi Anemia Research Fund (fanconi.org)
Cystinosis Clinical Presentation: History, Physical, Causes
Cystinosis Clinical Presentation: History, Physical, Causes (emedicine.medscape.com)
Pyridoxine-Dependent Epilepsy in Zebrafish Caused by Aldh7a1 Deficiency | Genetics
Pyridoxine-Dependent Epilepsy in Zebrafish Caused by Aldh7a1 Deficiency | Genetics (genetics.org)
WikiGenes - DEGS1 - delta(4)-desaturase, sphingolipid 1
WikiGenes - DEGS1 - delta(4)-desaturase, sphingolipid 1 (wikigenes.org)
Congenital_adrenal_hyperplasia
Congenital_adrenal_hyperplasia (bionity.com)
JIMD Reports - Case and Research Reports, 2012/3 | Verena Peters | Springer
JIMD Reports - Case and Research Reports, 2012/3 | Verena Peters | Springer (springer.com)
Mutagenesis as a Tool in Plant Genetics, Functional Genomics, and Breeding
Mutagenesis as a Tool in Plant Genetics, Functional Genomics, and Breeding (hindawi.com)
Von Willebrand disease | Genetics in Medicine
Von Willebrand disease | Genetics in Medicine (nature.com)
Plus it
Plus it (jneurosci.org)
Go to Allelic inactivation of the pseudoautosomal gene SYBL1 is controlled by epigenetic mechanisms common to the X and Y...
Go to Allelic inactivation of the pseudoautosomal gene SYBL1 is controlled by epigenetic mechanisms common to the X and Y... (igmm.cnrs.fr)
High resolution melting curve analysis enables rapid and reliable detection of G6PD variants in heterozygous females |...
High resolution melting curve analysis enables rapid and reliable detection of G6PD variants in heterozygous females |... (link.springer.com)
Transforming single DNA molecules into fluorescent magnetic particles for detection and enumeration of genetic variations | PNAS
Transforming single DNA molecules into fluorescent magnetic particles for detection and enumeration of genetic variations | PNAS (pnas.org)
WHO EMRO | Role of HFE gene mutations on developing iron overload in β-thalassaemia carriers in Egypt | Volume 17, issue 6 |...
WHO EMRO | Role of HFE gene mutations on developing iron overload in β-thalassaemia carriers in Egypt | Volume 17, issue 6 |... (emro.who.int)
Von Hippel-Lindau Syndrome Screening and Diagnosis
Von Hippel-Lindau Syndrome Screening and Diagnosis (news-medical.net)
Denaturing gradient gel electrophoresis for sale - 16407190
Denaturing gradient gel electrophoresis for sale - 16407190 (brakesband.com)
Wheat Landrace Genome Diversity | Genetics
Wheat Landrace Genome Diversity | Genetics (genetics.org)
Detection of Heterozygous Mutations in the Genome of Mismatch Repair Defective Diploid Yeast Using a Bayesian Approach |...
Detection of Heterozygous Mutations in the Genome of Mismatch Repair Defective Diploid Yeast Using a Bayesian Approach |... (genetics.org)
Leopard complex spotting in horses | Philosophical Transactions of the Royal Society B: Biological Sciences
Leopard complex spotting in horses | Philosophical Transactions of the Royal Society B: Biological Sciences (rstb.royalsocietypublishing.org)
Disorders of the Adrenal Cortex | GLOWM
Disorders of the Adrenal Cortex | GLOWM (glowm.com)
PCR technology: principles and applications for DNA amplification - Henry A. Erlich - Google Books
PCR technology: principles and applications for DNA amplification - Henry A. Erlich - Google Books (books.google.com.au)
An examination of the genotyping error detection function of SIMWALK2 | BMC Genetics | Full Text
An examination of the genotyping error detection function of SIMWALK2 | BMC Genetics | Full Text (bmcgenet.biomedcentral.com)
MLF Feature: Fractured Genetics
MLF Feature: Fractured Genetics (mountainlion.org)
A pilot to examine the logistical and feasibility issues in testing deceased tissue donors for vCJD using tonsil as the analyte...
A pilot to examine the logistical and feasibility issues in testing deceased tissue donors for vCJD using tonsil as the analyte... (link.springer.com)
GenePrint® 10 System
GenePrint® 10 System (promega.com)
Differential contributions of AF-1 and AF-2 activities to the developmental functions of RXRα | Development
Differential contributions of AF-1 and AF-2 activities to the developmental functions of RXRα | Development (dev.biologists.org)
US5981186A - Method and apparatus for DNA-sequencing using reduced number of sequencing mixtures - Google Patents
US5981186A - Method and apparatus for DNA-sequencing using reduced number of sequencing mixtures - Google Patents (patents.google.com)
Detection of Deleterious Genotypes in Multigenerational Studies. I. Disruptions in Individual Arabidopsis Actin Genes | Genetics
Detection of Deleterious Genotypes in Multigenerational Studies. I. Disruptions in Individual Arabidopsis Actin Genes | Genetics (genetics.org)