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1

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Genomic imprinting disorders in humans: a mini-review

per Butler, Merlin G.
Publicat 2009

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2

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Genomics of Childhood Obesity

per Butler, Merlin G
Publicat 2011

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3

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Prader-Willi Syndrome: Obesity due to Genomic Imprinting

per Butler, Merlin G
Publicat 2011

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4

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

per Butler, Merlin G.
Publicat a Prog Pediatr Cardiol (2005)

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5

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SISTER-CHROMATID EXCHANGE IN 4 HUMAN RACES

per BUTLER, MERLIN G.
Publicat a Mutat Res (1981)

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6

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PEDIATRIC HYPERTENSION: GENETICS OF HYPERTENSION • CURRENT STATUS

per Butler, Merlin G.
Publicat a J Med Liban (2010)

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7

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Imprinting Disorders: Non-Mendelian Mechanisms Affecting Growth

per Butler, Merlin G.
Publicat a J Pediatr Endocrinol Metab (2002)

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8

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

per Butler, Merlin G.
Publicat a Clin Dysmorphol (2000)

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9

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Benefits and Limitations of Prenatal Screening for Prader-Willi Syndrome

per Butler, Merlin G.
Publicat a Prenat Diagn (2016)

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10

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

per Butler, Merlin G.
Publicat a 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

per Butler, Merlin G.
Publicat a 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

per Butler, Merlin G.
Publicat a Hum Genet (1990)

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13

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

per BUTLER, MERLIN G.
Publicat a Compr Ther (1988)

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14

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

per Butler, Merlin G.
Publicat a J Intellect Disabil Res (2017)

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15

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Prader-Willi Syndrome: Current Understanding of Cause and Diagnosis

per Butler, Merlin G.
Publicat a 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?

per Butler, Merlin G.
Publicat a 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

per Butler, Merlin G.
Publicat a 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

per BUTLER, MERLIN G.
Publicat a Nebr Med J (1981)

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19

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Pharmacogenetics and Psychiatric Care: A Review and Commentary

per Butler, Merlin G.
Publicat a 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?

per Butler, Merlin G.
Publicat a Int J Mol Sci (2019)

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