Köhler MR - Search Results

1

Nephropathic cystinosis (CTNS-LSB): construction of a YAC contig comprising the refined critical region on chromosome 17p13.

Peters U, Senger G, Rählmann M, Du Chesne I, Stec I, Köhler MR, Weissenbach J, Leal SM, Koch HG, Deufel T, Harms E. Peters U, et al. Among authors: kohler mr. Eur J Hum Genet. 1997 Jan-Feb;5(1):9-14. Eur J Hum Genet. 1997. PMID: 9156315 Free PMC article.

2

Multiple minute marker chromosomes derived from Y identified by FISH in an intersexual infant.

Diekmann L, Palm K, Pfeiffer RA, Trautmann U, Scholz W, Schroers E, Vogt P, Köhler M. Diekmann L, et al. Hum Genet. 1992 Sep-Oct;90(1-2):181-3. doi: 10.1007/BF00210772. Hum Genet. 1992. PMID: 1427776

3

Selection of DNA sequences from interval 6 of the human Y chromosome with homology to a Y chromosomal fertility gene sequence of Drosophila hydei.

Vogt P, Keil R, Köhler M, Lengauer C, Lewe D, Lewe G. Vogt P, et al. Hum Genet. 1991 Feb;86(4):341-9. doi: 10.1007/BF00201830. Hum Genet. 1991. PMID: 1999335

4

Interstitial deletions of repetitive DNA blocks in dicentric human Y chromosomes.

Köhler MR, Vogt PH. Köhler MR, et al. Chromosoma. 1994 Sep;103(5):324-30. doi: 10.1007/BF00417879. Chromosoma. 1994. PMID: 7821087

5

Genomic organization and chromosomal localization of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene: a candidate for 6q-linked retinopathies.

Felbor U, Gehrig A, Sauer CG, Marquardt A, Köhler M, Schmid M, Weber BH. Felbor U, et al. Cytogenet Cell Genet. 1998;81(1):12-7. doi: 10.1159/000015001. Cytogenet Cell Genet. 1998. PMID: 9691169

6

Trisomy 2q35-q37 due to insertion of 2q material into 17q25: clinical, cytogenetic, and molecular cytogenetic characterization.

Fritz B, Müller-Navia J, Hillig U, Köhler M, Aslan M, Rehder H. Fritz B, et al. Am J Med Genet. 1999 Dec 3;87(4):297-301. Am J Med Genet. 1999. PMID: 10588833 Review.

7

A complex chromosome rearrangement involving chromosome 8, 11, and 12 analyzed by conventional cytogenetic investigations, fluorescence in situ hybridisation, and spectral karyotyping.

Kotzot D, Holland H, Köhler M, Froster UG. Kotzot D, et al. Ann Genet. 2001 Jul-Sep;44(3):135-8. doi: 10.1016/s0003-3995(01)01077-2. Ann Genet. 2001. PMID: 11694225

8

No FISH evidence for trisomy 7 in normal or leukemic bone marrow.

Köhler M, Johansson B, Garwicz S, Heim S, Mitelman F. Köhler M, et al. Cancer Genet Cytogenet. 1996 Jun;88(2):133-5. doi: 10.1016/0165-4608(95)00299-5. Cancer Genet Cytogenet. 1996. PMID: 8640721

9

Mutations in the human factor XII gene.

Schloesser M, Zeerleder S, Lutze G, Halbmayer WM, Hofferbert S, Hinney B, Koestering H, Lämmle B, Pindur G, Thies K, Köhler M, Engel W. Schloesser M, et al. Blood. 1997 Nov 15;90(10):3967-77. Blood. 1997. PMID: 9354665 Free article.

10

Refinement of the localization of the gene for neuronal nicotinic acetylcholine receptor alpha 4 subunit (CHRNA4) to human chromosome 20q13.2-q13.3.

Steinlein O, Smigrodzki R, Lindstrom J, Anand R, Köhler M, Tocharoentanaphol C, Vogel F. Steinlein O, et al. Genomics. 1994 Jul 15;22(2):493-5. doi: 10.1006/geno.1994.1420. Genomics. 1994. PMID: 7806245 Free article. No abstract available.

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