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Genomic imprinting disorders in humans: a mini-review

by Butler, Merlin G.
Published 2009

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Genomics of Childhood Obesity

by Butler, Merlin G
Published 2011

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Prader-Willi Syndrome: Obesity due to Genomic Imprinting

by Butler, Merlin G
Published 2011

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Progress in pediatric cardiology (“Genetics of Pediatric Heart Disease”)

by Butler, Merlin G.
Published in Prog Pediatr Cardiol (2005)

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5

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SISTER-CHROMATID EXCHANGE IN 4 HUMAN RACES

by BUTLER, MERLIN G.
Published in Mutat Res (1981)

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PEDIATRIC HYPERTENSION: GENETICS OF HYPERTENSION • CURRENT STATUS

by Butler, Merlin G.
Published in J Med Liban (2010)

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7

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Imprinting Disorders: Non-Mendelian Mechanisms Affecting Growth

by Butler, Merlin G.
Published in J Pediatr Endocrinol Metab (2002)

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A 68-year-old white female with Prader–Willi syndrome

by Butler, Merlin G.
Published in Clin Dysmorphol (2000)

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Benefits and Limitations of Prenatal Screening for Prader-Willi Syndrome

by Butler, Merlin G.
Published in Prenat Diagn (2016)

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FREQUENCY AND DISTRIBUTION OF CHROMOSOME FRAGILE SITES OR LESIONS IN MALES WITH MENTAL RETARDATION: A DESCRIPTIVE STUDY

by Butler, Merlin G.
Published in J Tenn Acad Sci (1998)

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11

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Sister Chromatid Exchanges in A Male With A Y/Y Translocation

by Butler, Merlin G.
Published in Trans Nebr Acad Sci Affil Soc (1981)

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12

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No significant relationship between age and frequency of chromosome lesions in mentally retarded individuals with or without the fragile X syndrome

by Butler, Merlin G.
Published in Hum Genet (1990)

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13

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Fragile X Syndrome: A Major Cause of X-Linked Mental Retardation

by BUTLER, MERLIN G.
Published in Compr Ther (1988)

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14

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Clinical and Genetic Aspects of the 15q11.2 BP1-BP2 Microdeletion Disorder

by Butler, Merlin G.
Published in J Intellect Disabil Res (2017)

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15

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Prader-Willi Syndrome: Current Understanding of Cause and Diagnosis

by Butler, Merlin G.
Published in Am J Med Genet (1990)

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16

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Are Specific Short Arm Variants or Heteromorphisms Over-Represented in the Chromosome 15 Deletion in Angelman or Prader-Willi Syndrome Patients?

by Butler, Merlin G.
Published in Am J Med Genet (1994)

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17

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Molecular Diagnosis of Prader-Willi Syndrome: Comparison of Cytogenetic and Molecular Genetic Data Including Parent of Origin Dependent Methylation DNA Patterns

by Butler, Merlin G.
Published in Am J Med Genet (1996)

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18

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Sister Chromatid Exchange Analysis in a 61 Year-old Female Using Various Medications

by BUTLER, MERLIN G.
Published in Nebr Med J (1981)

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19

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Pharmacogenetics and Psychiatric Care: A Review and Commentary

by Butler, Merlin G.
Published in J Ment Health Clin Psychol (2018)

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20

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Magnesium Supplement and the 15q11.2 BP1–BP2 Microdeletion (Burnside–Butler) Syndrome: A Potential Treatment?

by Butler, Merlin G.
Published in Int J Mol Sci (2019)

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