44 results on '"Butler, Merlin G."'
Search Results
2. Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes
3. A descriptive study on selected growth parameters and growth hormone receptor gene in healthy young adults from the American Midwest
4. Growth hormone receptor (GHR) gene polymorphism and scoliosis in Prader-Willi syndrome
5. Functional analysis of schizophrenia genes using GeneAnalytics program and integrated databases
6. Survival trends from the Prader–Willi Syndrome Association (USA) 40-year mortality survey
7. Causes of death in Prader-Willi syndrome: Prader-Willi Syndrome Association (USA) 40-year mortality survey
8. Prader-Willi syndrome and atypical submicroscopic 15q11-q13 deletions with or without imprinting defects
9. The High Direct Medical Costs of Prader-Willi Syndrome
10. High-resolution chromosome ideogram representation of recognized genes for bipolar disorder
11. Currently recognized clinically relevant and known genes for human reproduction and related infertility with representation on high-resolution chromosome ideograms
12. Laparoscopic sleeve gastrectomy in children and adolescents with Prader-Willi syndrome: a matched-control study
13. Change in psychiatric symptomatology after benfotiamine treatment in males is related to lifetime alcoholism severity
14. Clinically relevant genetic biomarkers from the brain in alcoholism with representation on high resolution chromosome ideograms
15. Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services
16. In This Issue
17. Frequency of Prader–Willi syndrome in births conceived via assisted reproductive technology
18. Double-blind, randomized placebo-controlled clinical trial of benfotiamine for severe alcohol dependence
19. IL1RAPL1 gene deletion as a cause of X-linked intellectual disability and dysmorphic features
20. Potential Sedation Risks in Prader-Willi Syndrome
21. snoTARGET shows that human orphan snoRNA targets locate close to alternative splice junctions
22. Whole genome microarray analysis of gene expression in subjects with fragile X syndrome
23. X chromosome gene expression in human tissues: Male and female comparisons
24. Clonality studies in sacral chordoma
25. C-reactive protein levels in subjects with Prader-Willi syndrome and obesity
26. Gene expression in pediatric heart disease with emphasis on conotruncal defects
27. Progress in pediatric cardiology (“Genetics of Pediatric Heart Disease”)
28. Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD
29. Diagnostic dilemma caused by overlapping features of Prader-Willi syndrome and trisomy 18 during infancy
30. Plasma leptin concentrations in lean and obese human subjects and Prader-Willi syndrome: Comparison of RIA and ELISA methods
31. Comparison of Chromosome Telomere Integrity in Multiple Tissues from Subjects at Different Ages
32. Clear Cell Sarcoma or Malignant Melanoma of Soft Parts
33. Microsatellite Instability in Malignant Melanoma
34. The Presence of Genetic Anticipation Suggests That the Molecular Basis of Familial Primary Pulmonary Hypertension May Be Trinucleotide Repeat Expansion
35. Lack of microsatellite instability in giant cell tumor of bone
36. Chromosome telomere integrity of human solid neoplasms
37. Cytogenetic, telomere, and telomerase studies in five surgically managed lumbosacral chordomas
38. Telomere reduction in giant cell tumor of bone and with aging
39. Molecular analysis of transforming growth factor beta in giant cell tumor of bone
40. Telomeric associations and consistent growth factor overexpression detected in giant cell tumor of bone
41. Increased frequency of sister-chromatid exchanges in alcoholics
42. Sister-chromatid exchange in 4 human races
43. Urticaria pigmentosa in a child with Prader-Labhart-Willi syndrome
44. A child with 45,X/46,X,del(Y)(q12) identified with a Y-specific probe
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