Clinical Assessment, Genetics, and Treatment Approaches in Autism Spectrum Disorder (ASD) von Genovese, Ann, Butler, Merlin G

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Prader-Willi Syndrome and Chromosome 15q11.2 BP1-BP2 Region: A Review von Butler, Merlin G

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Prader-Willi Syndrome: Obesity due to Genomic Imprinting von Butler, Merlin G

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Genetics of Obesity in Humans: A Clinical Review von Mahmoud, Ranim, Kimonis, Virginia, Butler, Merlin G

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The Autism Spectrum: Behavioral, Psychiatric and Genetic Associations von Genovese, Ann, Butler, Merlin G

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Magnesium Supplement and the 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) Syndrome: A Potential Treatment? von Butler, Merlin G

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The 15q11.2 BP1-BP2 microdeletion syndrome: a review von Cox, Devin M, Butler, Merlin G

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Genomic imprinting disorders in humans: a mini-review von Butler, Merlin G.

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Causes of death in Prader-Willi syndrome: Prader-Willi Syndrome Association (USA) 40-year mortality survey von Butler, Merlin G., Manzardo, Ann M., Heinemann, Janalee, Loker, Carolyn, Loker, James

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Pine bark valorization by activated carbons production to be used as VOCs adsorbents von Sessa, F., Merlin, G., Canu, P.

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Clinical Trials in Prader-Willi Syndrome: A Review von Mahmoud, Ranim, Kimonis, Virginia, Butler, Merlin G

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The 15q11.2 BP1-BP2 Microdeletion ( Burnside-Butler ) Syndrome: In Silico Analyses of the Four Coding Genes Reveal Functional Associations with Neurodevelopmental Phenotypes von Rafi, Syed K, Butler, Merlin G

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Prader–Willi syndrome, deletion subtypes, and magnesium: Potential impact on clinical findings von Butler, Merlin G., Cowen, Neil, Bhatnagar, Anish

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Benefits and limitations of prenatal screening for Prader–Willi syndrome von Butler, Merlin G.

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Genetics of anomalies of the kidney and urinary tract with congenital heart disease: A review von Barakat, Amin J., Butler, Merlin G.

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Rare FMR1 gene mutations causing fragile X syndrome: A review von Sitzmann, Adam F., Hagelstrom, Robert T., Tassone, Flora, Hagerman, Randi J., Butler, Merlin G.

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Survival trends from the Prader–Willi Syndrome Association (USA) 40-year mortality survey von Manzardo, Ann M., Loker, James, Heinemann, Janalee, Loker, Carolyn, Butler, Merlin G.

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Enhancing PAPR performance in MIMO-OFDM system using hybrid optimal MMSE-MLSE equalizers von Krishna Reddy, G., Merlin Sheeba, G.

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Functional analysis of schizophrenia genes using GeneAnalytics program and integrated databases von Sundararajan, Tharani, Manzardo, Ann M., Butler, Merlin G.

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Genetic conditions of short stature: A review of three classic examples von Butler, Merlin G., Miller, Bradley S., Romano, Alicia, Ross, Judith, Abuzzahab, M. Jennifer, Backeljauw, Philippe, Bamba, Vaneeta, Bhangoo, Amrit, Mauras, Nelly, Geffner, Mitchell

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