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. Survival trends from the Prader–Willi Syndrome Association (USA) 40-year mortality survey
6. Causes of death in Prader-Willi syndrome: Prader-Willi Syndrome Association (USA) 40-year mortality survey
7. Prader-Willi syndrome and atypical submicroscopic 15q11-q13 deletions with or without imprinting defects
8. The High Direct Medical Costs of Prader-Willi Syndrome
9. Laparoscopic sleeve gastrectomy in children and adolescents with Prader-Willi syndrome: a matched-control study
10. Frequency of Prader–Willi syndrome in births conceived via assisted reproductive technology
11. Whole genome microarray analysis of gene expression in subjects with fragile X syndrome
12. X chromosome gene expression in human tissues: Male and female comparisons
13. Gene expression in pediatric heart disease with emphasis on conotruncal defects
14. Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD
15. Chapter One - Single Gene and Syndromic Causes of Obesity: Illustrative Examples
16. Analysis of imprinted genes in subjects with Prader-Willi syndrome and chromosome 15 abnormalities
17. Plasma leptin concentrations in lean and obese human subjects and Prader-Willi syndrome: Comparison of RIA and ELISA methods
18. IL1RAPL1 gene deletion as a cause of X-linked intellectual disability and dysmorphic features
19. Clonality studies in sacral chordoma
20. C-reactive protein levels in subjects with Prader-Willi syndrome and obesity
21. In This Issue
22. Diagnostic dilemma caused by overlapping features of Prader-Willi syndrome and trisomy 18 during infancy
23. Progress in pediatric cardiology (“Genetics of Pediatric Heart Disease”)
24. Sister-chromatid exchange in 4 human races
25. Molecular analysis of transforming growth factor beta in giant cell tumor of bone
26. Dosage and allelic restriction fragment studies and PCR analysis of the H- ras locus in giant cell tumor of bone
27. Cytogenetic abnormalities in a rare case of giant cell osteogenic sarcoma
28. Telomeric associations and consistent growth factor overexpression detected in giant cell tumor of bone
29. Telomere reduction in giant cell tumor of bone and with aging
30. Cytogenetic studies of individuals from four kindreds with multiple endocrine neoplasia type II syndrome
31. High resolution chromosome and DNA analysis in multiple endocrine neoplasia type II syndrome
32. Clear Cell Sarcoma or Malignant Melanoma of Soft Parts: Molecular Analysis of Microsatellite Instability with Clinical Correlation
33. Comparison of Chromosome Telomere Integrity in Multiple Tissues from Subjects at Different Ages
34. Microsatellite Instability in Malignant Melanoma
35. Lack of microsatellite instability in giant cell tumor of bone
36. Cytogenetic, telomere, and telomerase studies in five surgically managed lumbosacral chordomas
37. Chromosome telomere integrity of human solid neoplasms
38. Increased frequency of sister-chromatid exchanges in alcoholics
39. Effects of age, sex and multiple endocrine neoplasia type-II on silver stained nucleolar organizer regions
40. The Presence of Genetic Anticipation Suggests That the Molecular Basis of Familial Primary Pulmonary Hypertension May Be Trinucleotide Repeat Expansion
41. Analysis of 13q RFLP in multiple endocrine neoplasia type II kindreds
42. A child with 45,X/46,X,del(Y)(q12) identified with a Y-specific probe
43. Urticaria pigmentosa in a child with Prader-Labhart-Willi syndrome
44. A Possible Etiology of the Infertile 46XX Male Subject
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.