Zobrazeno 1 - 10 of 73 pro vyhledávání: '"D L Van Dyke"'
1
A unique radar calibration target
Autor: J. E. Heine, D. L. Van Dyke, J. N. Devlin
Publikováno v: IEEE Aerospace and Electronic Systems Magazine. 27:8-15
The new family of radar targets, described herein, provides the radar operator with a clutter-free point source and a reliable means of assessing overall radar operation and performance on a continuous or periodic basis. Prior to this technology, per
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0b033e5f67918236d067d6ad690dd695
https://doi.org/10.1109/maes.2012.6203713
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4
Cytogenetic analysis and construction of a BAC contig across a common neocentromeric region from 9p
Autor: Gail H. Vance, D. L. Satinover, Stuart Schwartz, D. L. Van Dyke
Publikováno v: Chromosoma. 110:275-283
Over 40 cases of neocentric marker chromosomes, without detectable alpha-satellite DNA, have been reported. Although these have originated from many different chromosomes, a few of these chromosomes have been involved in multiple cases of marker form
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3fa0af9680babf9653a123a27cd31a6
https://doi.org/10.1007/s004120100143
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5
Deletion of 2q37 and duplication of 10q24: Two cases in the same family and review of the literature
Autor: P M Czarnecki, D. L. Van Dyke, G.L. Feldman, E.V. Bawle, J.V. Conard, Anne E. Wiktor
Publikováno v: Annales de Génétique. 44:129-134
We describe two patients (first cousins, once removed) with an unusual head shape, high arched palate, flat nasal bridge, abnormal ears, hand and feet abnormalities and other anomalies. The patients were ascertained independently and it was initially
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7f1ea624810a53a6a58942b336867c8
https://doi.org/10.1016/s0003-3995(01)01083-8
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7
Replication banding and molecular studies of a mosaic, unbalanced dic(X;15)(xpter→xq26.1::15p11→15qter)
Autor: D. L. Van Dyke, Lisa G. Shaffer, Angela Scheuerle, David H. Ledbetter, Frank Greenberg, J. L. Zenger-Hain
Publikováno v: American Journal of Medical Genetics. 56:403-408
We present a patient with a chromosomal mosaicism involving the X chromosome. One cell line is 45,X and the other has a de novo paternally derived dicentric X;15 translocation. Her karyotype is therefore 45,X/45,X,dic(X;15)(Xpter {yields} Xq26.1::15p
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c11b987f6ec855cc2656928ae26c655
https://doi.org/10.1002/ajmg.1320560411
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8
Paracentric inversions in humans: A review of 446 paracentric inversions with presentation of 120 new cases
Autor: C. G. Palmer, F. Elder, J. T. Lanman, S. Schwartz, Mark J. Pettenati, M. D. Higgins, Elisabeth A. Keitges, J. Brown, Kathleen W. Rao, F. Grass, R. R. Higgins, M. G. Butler, D. L. Van Dyke, Colleen Jackson-Cook, P. N. Rao, J. L. Smith, P. Cosper, A. J. Carroll, M. C. Phelan, F.W. Luthardt
Publikováno v: American Journal of Medical Genetics. 55:171-187
We present a large review of 446 cases of paracentric inversions (PAI), including 120 new cases, to assess their incidence, distribution, inheritance, modes of ascertainment, interchromosomal effects, viable recombinant offspring, and clinical releva
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ad6689bada096de7e20dfc060bea522
https://doi.org/10.1002/ajmg.1320550207
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9
Leukemia risk models in primary myelofibrosis: an International Working Group study
Autor: A Tefferi, Mario Cazzola, Francisco Cervantes, D L Van Dyke, Kebede H. Begna, E. Morra, Naseema Gangat, Alessandro M. Vannucchi, Francesco Passamonti, C A Hanson, A. Pardanani, Domenica Caramazza, Arturo Pereira
Publikováno v: Leukemia. 26(6)
Abstract 3833 Background: Survival in primary myelofibrosis (PMF) is assessed by the Dynamic International Prognostic Scoring System (DIPSS) (Blood 2010;115:1703) and DIPSS-plus (JCO 2011;29:392). The latter is based on eight risk factors including a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bce4a79d28a0166c8be94f2e28af9fa5
https://pubmed.ncbi.nlm.nih.gov/22289985
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10
Refined cytogenetic-risk categorization for overall and leukemia-free survival in primary myelofibrosis: a single center study of 433 patients
Autor: Animesh Pardanani, Naseema Gangat, A Tefferi, C A Hanson, Kebede H. Begna, Domenica Caramazza, Rakhee Vaidya, D L Van Dyke, Sergio Siragusa
Publikováno v: Leukemia
We have previously identified sole +9, 13q- or 20q-, as 'favorable' and sole +8 or complex karyotype as 'unfavorable' cytogenetic abnormalities in primary myelofibrosis (PMF). In this study of 433 PMF patients, we describe additional sole abnormaliti
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f30f5a1a22ac11f1be3903f9d2438c50
http://hdl.handle.net/10447/75836
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