Korn B - Search Results

1

MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM.

Vits L, Van Camp G, Coucke P, Fransen E, De Boulle K, Reyniers E, Korn B, Poustka A, Wilson G, Schrander-Stumpel C, et al. Vits L, et al. Among authors: korn b. Nat Genet. 1994 Jul;7(3):408-13. doi: 10.1038/ng0794-408. Nat Genet. 1994. PMID: 7920660

2

Fragile X syndrome without CCG amplification has an FMR1 deletion.

Gedeon AK, Baker E, Robinson H, Partington MW, Gross B, Manca A, Korn B, Poustka A, Yu S, Sutherland GR, et al. Gedeon AK, et al. Among authors: korn b. Nat Genet. 1992 Aug;1(5):341-4. doi: 10.1038/ng0892-341. Nat Genet. 1992. PMID: 1302032

3

Completion of the physical map of Xq28: the location of the gene for L1CAM on the human X chromosome.

Dietrich A, Korn B, Poustka A. Dietrich A, et al. Among authors: korn b. Mamm Genome. 1992;3(3):168-72. doi: 10.1007/BF00352462. Mamm Genome. 1992. PMID: 1617223

4

Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene.

Dittrich B, Buiting K, Korn B, Rickard S, Buxton J, Saitoh S, Nicholls RD, Poustka A, Winterpacht A, Zabel B, Horsthemke B. Dittrich B, et al. Among authors: korn b. Nat Genet. 1996 Oct;14(2):163-70. doi: 10.1038/ng1096-163. Nat Genet. 1996. PMID: 8841186

5

Distribution and early development of microarray technology in Europe.

Vente A, Korn B, Zehetner G, Poustka A, Lehrach H. Vente A, et al. Among authors: korn b. Nat Genet. 1999 May;22(1):22. doi: 10.1038/8734. Nat Genet. 1999. PMID: 10319856 No abstract available.

6

DMBT1, a new member of the SRCR superfamily, on chromosome 10q25.3-26.1 is deleted in malignant brain tumours.

Mollenhauer J, Wiemann S, Scheurlen W, Korn B, Hayashi Y, Wilgenbus KK, von Deimling A, Poustka A. Mollenhauer J, et al. Among authors: korn b. Nat Genet. 1997 Sep;17(1):32-9. doi: 10.1038/ng0997-32. Nat Genet. 1997. PMID: 9288095

7

A strategy for the selection of transcribed sequences in the Xq28 region.

Korn B, Sedlacek Z, Manca A, Kioschis P, Konecki D, Lehrach H, Poustka A. Korn B, et al. Hum Mol Genet. 1992 Jul;1(4):235-42. doi: 10.1093/hmg/1.4.235. Hum Mol Genet. 1992. PMID: 1303192

8

A microdeletion of less than 250 kb, including the proximal part of the FMR-I gene and the fragile-X site, in a male with the clinical phenotype of fragile-X syndrome.

Wöhrle D, Kotzot D, Hirst MC, Manca A, Korn B, Schmidt A, Barbi G, Rott HD, Poustka A, Davies KE, et al. Wöhrle D, et al. Among authors: korn b. Am J Hum Genet. 1992 Aug;51(2):299-306. Am J Hum Genet. 1992. PMID: 1642231 Free PMC article.

9

Expression patterns of two human genes coding for different rab GDP-dissociation inhibitors (GDIs), extremely conserved proteins involved in cellular transport.

Bächner D, Sedlacek Z, Korn B, Hameister H, Poustka A. Bächner D, et al. Among authors: korn b. Hum Mol Genet. 1995 Apr;4(4):701-8. doi: 10.1093/hmg/4.4.701. Hum Mol Genet. 1995. PMID: 7543319

10

Model for a transcript map of human chromosome 21: isolation of new coding sequences from exon and enriched cDNA libraries.

Yaspo ML, Gellen L, Mott R, Korn B, Nizetic D, Poustka AM, Lehrach H. Yaspo ML, et al. Among authors: korn b. Hum Mol Genet. 1995 Aug;4(8):1291-304. doi: 10.1093/hmg/4.8.1291. Hum Mol Genet. 1995. PMID: 7581366

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