146 results on '"Butler, Merlin G."'
Search Results
2. Next‐generation sequencing and analysis of consecutive patients referred for connective tissue disorders
3. Syndromic and Nonsyndromic Obesity: Underlying Genetic Causes in Humans
4. Critical review of bariatric surgical outcomes in patients with Prader‐Willi syndrome and other hyperphagic disorders
5. PHIPgene variants with protein modeling, interactions, and clinical phenotypes
6. Influence of molecular classes and growth hormone treatment on growth and dysmorphology in Prader‐Willi syndrome: A multicenter study
7. ADAMTSL2gene variant in patients with features of autosomal dominant connective tissue disorders
8. Impact of genetic subtypes of Prader–Willi syndrome with growth hormone therapy on intelligence and body mass index
9. Birth seasonality studies in a large Prader–Willi syndrome cohort
10. Analysis of the Prader–Willi syndrome imprinting center using droplet digital PCR and next‐generation whole‐exome sequencing
11. Contributing factors of mortality in Prader–Willi syndrome
12. Newborn screening for Prader–Willi syndrome is feasible: Early diagnosis for better outcomes
13. Preliminary observations of mitochondrial dysfunction in Prader-Willi syndrome
14. Tobacco and cannabis use in college students are predicted by sex‐dimorphic interactions betweenMAOAgenotype and child abuse
15. Three siblings with Prader–Willi syndrome caused by imprinting center microdeletions and review
16. Prader–Willi syndrome and early‐onset morbid obesity NIH rare disease consortium: A review of natural history study
17. Rare FMR1 gene mutations causing fragile X syndrome: A review
18. Effects of MetAP2 inhibition on hyperphagia and body weight in Prader–Willi syndrome: A randomized, double‐blind, placebo‐controlled trial
19. Exploring genetic susceptibility to obesity through genome functional pathway analysis
20. Oxytocin treatment in children with Prader–Willi syndrome: A double‐blind, placebo‐controlled, crossover study
21. Benefits and limitations of prenatal screening for Prader-Willi syndrome
22. Higher plasma orexin a levels in children with Prader-Willi syndrome compared with healthy unrelated sibling controls
23. Elevated plasma oxytocin levels in children with Prader-Willi syndrome compared with healthy unrelated siblings
24. Transcranial direct current stimulation reduces food-craving and measures of hyperphagia behavior in participants with Prader-Willi syndrome
25. Currently recognized genes for schizophrenia: High-resolution chromosome ideogram representation
26. High plasma neurotensin levels in children with Prader–Willi syndrome
27. Metabolic profiling in Prader-Willi syndrome and nonsyndromic obesity: sex differences and the role of growth hormone
28. Increased plasma chemokine levels in children with Prader–Willi syndrome
29. Exon Microarray Analysis of Human Dorsolateral Prefrontal Cortex in Alcoholism
30. Hyperphagia: Current concepts and future directions proceedings of the 2nd international conference on hyperphagia
31. Growth hormone receptor (GHR) gene polymorphism and prader-willi syndrome
32. Development and implementation of electronic growth charts for infants with Prader-Willi syndrome
33. X Chromosome Inactivation in Women with Alcoholism
34. The neuroanatomy of genetic subtype differences in Prader-Willi syndrome
35. Nutritional phases in Prader–Willi syndrome
36. TPH2 G/T polymorphism is associated with hyperphagia, IQ, and internalizing problems in Prader-Willi syndrome
37. Erratum to: An Interstitial 15q11-q14 Deletion: Expanded Prader-Willi Syndrome Phenotype (DOI 10.1002/ajmg.a.33197; Am J Med Genet Part A 152A:404-408)
38. Neural Mechanisms Associated With Food Motivation in Obese and Healthy Weight Adults
39. An interstitial 15q11-q14 deletion: Expanded Prader-Willi syndrome phenotype
40. An 18-year follow-up report on an infant with a duplication of 9q34
41. Cortisol levels in Prader-Willi syndrome support changes and routine care
42. Morning melatonin levels in Prader-Willi syndrome
43. Cortisol levels in Prader-Willi syndrome support changes in routine care
44. Feasibility and relevance of examining lymphoblastoid cell lines to study role of microRNAs in autism
45. Photoanthropometric study of craniofacial traits in individuals with Prader-Willi syndrome on short-term growth hormone therapy
46. Antley-Bixler syndrome: report of a patient and review of literature
47. Anthropometric study with emphasis on hand and foot measurements in the Prader-Willi syndrome: sex, age and chromosome effects
48. Robinow syndrome: report of two patients and review of literature
49. A 15-item checklist for screening mentally retarded males for the fragile X syndrome
50. Genetic variants of the human obesity (OB) gene in subjects with and without Prader-Willi syndrome: comparison with body mass index and weight
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.