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Publications by Merlin G. Butler
Bi-Allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes
American Journal of Human Genetics
Genetics
Double-Blind, Randomized Placebo-Controlled Clinical Trial of Benfotiamine for Severe Alcohol Dependence
Drug and Alcohol Dependence
Psychiatry
Toxicology
Mental Health
Pharmacology
Birth Seasonality Studies in a Large Prader-Willi Syndrome Cohort
American Journal of Medical Genetics, Part A
Genetics
Comparison of Biological Specimens and DNA Collection Methods for PCR Amplification and Microarray Analysis
Clinical Chemistry and Laboratory Medicine
Biochemistry
Medicine
Clinical Biochemistry
Analysis of the Prader-Willi Syndrome Imprinting Center Using Droplet Digital PCR and Next-Generation Whole-Exome Sequencing
Molecular genetics & genomic medicine
Genetics
Molecular Biology
A Child With 45,x/46,X,del(Y)(q12) Identified With a Y-Specific Probe
Fertility and Sterility
Gynecology
Reproductive Medicine
Obstetrics
A 15-Item Checklist for Screening Mentally Retarded Males for the Fragile X Syndrome
Clinical Genetics
Genetics
Metacarpophalangeal Pattern Profile Analysis in Clinical Genetics: An Applied Anthropometric Method
American Journal of Physical Anthropology
Anatomy
Anthropology
A 9-Year-Old Male With a Duplication of Chromosome 3p25.3p26.2: Clinical Report and Gene Expression Analysis
American Journal of Medical Genetics, Part A
Genetics
Deaths Due to Choking in Prader–Willi Syndrome
American Journal of Medical Genetics, Part A
Genetics
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