Zobrazeno 1 - 8
of 8
pro vyhledávání: '"L J, Raffel"'
Autor:
H. A. Erlich, J. I. Rotter, J. D. Chang, S. J. Shaw, L. J. Raffel, W. Klitz, T. L. Bugawan, A. Zeidler
Publikováno v:
Diabetes. 45:610-614
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a8f29f2ed5abc7f9d2b0c4b4f8896ad8
https://doi.org/10.2337/diabetes.45.5.610
https://doi.org/10.2337/diabetes.45.5.610
Publikováno v:
American journal of medical genetics. 71(3)
Targeting individuals with increased risk for common, chronic disease can improve the efficiency and efficacy of preventive efforts by improving the predictability of screening tests and participant compliance. Individuals with the greatest risk for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::224bdffbf5dbdf6db637d3150aa3e3c8
https://pubmed.ncbi.nlm.nih.gov/9268102
https://pubmed.ncbi.nlm.nih.gov/9268102
Autor:
J, Leana-Cox, S, Levin, R, Surana, E, Wulfsberg, C L, Keene, L J, Raffel, B, Sullivan, S, Schwartz
Publikováno v:
American journal of human genetics. 52(6)
Fluorescence in situ hybridization (FISH) with chromosome-specific DNA libraries was performed on samples from eight patients with de novo chromosomal duplications. In five cases, the clinical phenotype and/or cytogenetic evaluations suggested a like
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aecc528ab43f6f7d644af59297a6db84
https://pubmed.ncbi.nlm.nih.gov/8503441
https://pubmed.ncbi.nlm.nih.gov/8503441
Publikováno v:
Journal of medical genetics. 29(7)
Population studies have suggested an increased frequency of small DNA insertions (class I alleles) 5' to the insulin gene in insulin dependent (type I) diabetes mellitus (IDDM). The present study examined this relationship within families. Forty-one
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::65af3b493f5e2afe64cf0633c97d5c99
https://pubmed.ncbi.nlm.nih.gov/1353534
https://pubmed.ncbi.nlm.nih.gov/1353534
Publikováno v:
Annales de genetique. 33(2)
A family is reported in which a man with a balanced reciprocal translocation [46,XY,t(7;22)(q32;q13.3)] fathered a daughter who was trisomic for the region 7q32----7qter and monosomic for 22q13.3----22qter, and a male fetus who was monosomic for 7q32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::33de3bd342f19fdad903bfbe3701fdb0
https://pubmed.ncbi.nlm.nih.gov/2241085
https://pubmed.ncbi.nlm.nih.gov/2241085
Publikováno v:
Archives of pathologylaboratory medicine. 110(7)
We report an incidental microscopic finding of ectopic renal tissue in a newborn with multiple congenital anomalies. The ectopic renal tissue was located in the wall of the distal blind end of the colon. The tissue was composed of undifferentiated re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::079f9f0b6bc9ae02e423f8d0b6f00c0a
https://pubmed.ncbi.nlm.nih.gov/3013121
https://pubmed.ncbi.nlm.nih.gov/3013121
Publikováno v:
Maryland medical journal (Baltimore, Md. : 1985). 38(11)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b97bb4568e516c0e94d2c0ba3002ee41
https://pubmed.ncbi.nlm.nih.gov/2685498
https://pubmed.ncbi.nlm.nih.gov/2685498
Publikováno v:
Progress in clinical and biological research. 147
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4c11e86e78e995b5fadd8eafd481525b
https://pubmed.ncbi.nlm.nih.gov/6429664
https://pubmed.ncbi.nlm.nih.gov/6429664