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作者
Butler, Merlin G.
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Genomic imprinting disorders in humans: a mini-review
由
Butler
,
Merlin
G
.
出版 2009
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Genomics of Childhood Obesity
由
Butler
,
Merlin
G
出版 2011
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Prader-Willi Syndrome: Obesity due to Genomic Imprinting
由
Butler
,
Merlin
G
出版 2011
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Progress in pediatric cardiology (“Genetics of Pediatric Heart Disease”)
由
Butler
,
Merlin
G
.
發表在
Prog Pediatr Cardiol
(2005)
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SISTER-CHROMATID EXCHANGE IN 4 HUMAN RACES
由
BUTLER
,
MERLIN
G
.
發表在
Mutat Res
(1981)
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PEDIATRIC HYPERTENSION: GENETICS OF HYPERTENSION • CURRENT STATUS
由
Butler
,
Merlin
G
.
發表在
J Med Liban
(2010)
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Imprinting Disorders: Non-Mendelian Mechanisms Affecting Growth
由
Butler
,
Merlin
G
.
發表在
J Pediatr Endocrinol Metab
(2002)
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A 68-year-old white female with Prader–Willi syndrome
由
Butler
,
Merlin
G
.
發表在
Clin Dysmorphol
(2000)
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Benefits and Limitations of Prenatal Screening for Prader-Willi Syndrome
由
Butler
,
Merlin
G
.
發表在
Prenat Diagn
(2016)
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FREQUENCY AND DISTRIBUTION OF CHROMOSOME FRAGILE SITES OR LESIONS IN MALES WITH MENTAL RETARDATION: A DESCRIPTIVE STUDY
由
Butler
,
Merlin
G
.
發表在
J Tenn Acad Sci
(1998)
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Sister Chromatid Exchanges in A Male With A Y/Y Translocation
由
Butler
,
Merlin
G
.
發表在
Trans Nebr Acad Sci Affil Soc
(1981)
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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
由
Butler
,
Merlin
G
.
發表在
Hum Genet
(1990)
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Fragile X Syndrome: A Major Cause of X-Linked Mental Retardation
由
BUTLER
,
MERLIN
G
.
發表在
Compr Ther
(1988)
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Clinical and Genetic Aspects of the 15q11.2 BP1-BP2 Microdeletion Disorder
由
Butler
,
Merlin
G
.
發表在
J Intellect Disabil Res
(2017)
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Prader-Willi Syndrome: Current Understanding of Cause and Diagnosis
由
Butler
,
Merlin
G
.
發表在
Am J Med Genet
(1990)
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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?
由
Butler
,
Merlin
G
.
發表在
Am J Med Genet
(1994)
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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
由
Butler
,
Merlin
G
.
發表在
Am J Med Genet
(1996)
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Sister Chromatid Exchange Analysis in a 61 Year-old Female Using Various Medications
由
BUTLER
,
MERLIN
G
.
發表在
Nebr Med J
(1981)
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Pharmacogenetics and Psychiatric Care: A Review and Commentary
由
Butler
,
Merlin
G
.
發表在
J Ment Health Clin Psychol
(2018)
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Magnesium Supplement and the 15q11.2 BP1–BP2 Microdeletion (Burnside–Butler) Syndrome: A Potential Treatment?
由
Butler
,
Merlin
G
.
發表在
Int J Mol Sci
(2019)
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15q11.2
15q11.2 BP1-BP2 deletion
15q11.2 BP1-BP2 microdeletion (Burnside-Butler) syndrome
15q11.2 BP1–BP2 microdeletion (Burnside–Butler syndrome)
22q13.3 duplication
AMPA receptors
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IL-6
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