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Spectrum of small length germline mutations in the RB1 gene.
Lohmann DR, Brandt B, Höpping W, Passarge E, Horsthemke B. Lohmann DR, et al. Hum Mol Genet. 1994 Dec;3(12):2187-93. doi: 10.1093/hmg/3.12.2187. Hum Mol Genet. 1994. PMID: 7881418
PCR-mediated cloning of HpaII tiny fragments from microdissected human chromosomes.
Horsthemke B, Claussen U, Hesse S, Lüdecke HJ. Horsthemke B, et al. PCR Methods Appl. 1992 May;1(4):229-33. doi: 10.1101/gr.1.4.229. PCR Methods Appl. 1992. PMID: 1282430
Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis.
Kuwano A, Mutirangura A, Dittrich B, Buiting K, Horsthemke B, Saitoh S, Niikawa N, Ledbetter SA, Greenberg F, Chinault AC, et al. Kuwano A, et al. Hum Mol Genet. 1992 Sep;1(6):417-25. doi: 10.1093/hmg/1.6.417. Hum Mol Genet. 1992. PMID: 1363801
Genetics and cytogenetics of retinoblastoma.
Horsthemke B. Horsthemke B. Cancer Genet Cytogenet. 1992 Oct 1;63(1):1-7. doi: 10.1016/0165-4608(92)90055-d. Cancer Genet Cytogenet. 1992. PMID: 1423220 Review.
Deletion in one allele and a rare neutral DNA alteration in the other allele of the RB1 gene in a patient with bilateral retinoblastoma.
Horsthemke B, Brandt B, Albrecht B, Passarge E. Horsthemke B, et al. Am J Med Genet. 1992 Sep 15;44(2):255. doi: 10.1002/ajmg.1320440235. Am J Med Genet. 1992. PMID: 1456305 No abstract available.
Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13.
Dittrich B, Robinson WP, Knoblauch H, Buiting K, Schmidt K, Gillessen-Kaesbach G, Horsthemke B. Dittrich B, et al. Hum Genet. 1992 Nov;90(3):313-5. doi: 10.1007/BF00220089. Hum Genet. 1992. PMID: 1487250
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