Hofker M - Search Results

1

Sublocalization of the synovial sarcoma-associated t(X;18) chromosomal breakpoint in Xp11.2 using cosmid cloning and fluorescence in situ hybridization.

de Leeuw B, Suijkerbuijk RF, Balemans M, Sinke RJ, de Jong B, Molenaar WM, Meloni AM, Sandberg AA, Geraghty M, Hofker M, et al. de Leeuw B, et al. Among authors: hofker m. Oncogene. 1993 Jun;8(6):1457-63. Oncogene. 1993. PMID: 8389029

2

Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35.

Wijmenga C, Dauwerse HG, Padberg GW, Meyer N, Murray JC, Mills K, van Ommen GB, Hofker MH, Frants RR. Wijmenga C, et al. Among authors: hofker mh. Muscle Nerve Suppl. 1995;2:S14-8. Muscle Nerve Suppl. 1995. PMID: 7739620 Free article.

3

Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35.

Wijmenga C, Dauwerse HG, Padberg GW, Meyer N, Murray JC, Mills K, van Ommen GB, Hofker MH, Frants RR. Wijmenga C, et al. Among authors: hofker mh. Muscle Nerve Suppl. 1995;(2):S14-8. Muscle Nerve Suppl. 1995. PMID: 23573581

4

Genomic cloning of the mouse LDL receptor related protein/alpha 2-macroglobulin receptor gene.

van der Zee A, Stas L, Hilleker C, van Leuven F, van Dijk KW, Havekes L, Frants R, Hofker M. van der Zee A, et al. Among authors: hofker m. Genomics. 1994 Sep 1;23(1):256-9. doi: 10.1006/geno.1994.1489. Genomics. 1994. PMID: 7829084

5

The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus.

Wijmenga C, Winokur ST, Padberg GW, Skraastad MI, Altherr MR, Wasmuth JJ, Murray JC, Hofker MH, Frants RR. Wijmenga C, et al. Among authors: hofker mh. Hum Genet. 1993 Sep;92(2):198-203. doi: 10.1007/BF00219692. Hum Genet. 1993. PMID: 8103757

6

Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35.

van Deutekom JC, Hofker MH, Romberg S, van Geel M, Rommens J, Wright TJ, Hewitt JE, Padberg GW, Wijmenga C, Frants RR. van Deutekom JC, et al. Among authors: hofker mh. Muscle Nerve Suppl. 1995;(2):S19-26. Muscle Nerve Suppl. 1995. PMID: 23573582

7

Genomic structure and evolution of the human pepsinogen A multigene family.

Zelle B, Evers MP, Groot PC, Bebelman JP, Mager WH, Planta RJ, Pronk JC, Meuwissen SG, Hofker MH, Eriksson AW, et al. Zelle B, et al. Among authors: hofker mh. Hum Genet. 1988 Jan;78(1):79-82. doi: 10.1007/BF00291240. Hum Genet. 1988. PMID: 2892778

8

Inter- and intrachromosomal sub-telomeric rearrangements on 4q35: implications for facioscapulohumeral muscular dystrophy (FSHD) aetiology and diagnosis.

Lemmers RJ, van der Maarel SM, van Deutekom JC, van der Wielen MJ, Deidda G, Dauwerse HG, Hewitt J, Hofker M, Bakker E, Padberg GW, Frants RR. Lemmers RJ, et al. Among authors: hofker m. Hum Mol Genet. 1998 Aug;7(8):1207-14. doi: 10.1093/hmg/7.8.1207. Hum Mol Genet. 1998. PMID: 9668160

9

Evolutionary conservation of the mouse apolipoprotein e-c1-c2 gene cluster: structure and genetic variability in inbred mice.

Hoffer MJ, Hofker MH, van Eck MM, Havekes LM, Frants RR. Hoffer MJ, et al. Among authors: hofker mh. Genomics. 1993 Jan;15(1):62-7. doi: 10.1006/geno.1993.1010. Genomics. 1993. PMID: 7916738

10

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy.

Wijmenga C, Hewitt JE, Sandkuijl LA, Clark LN, Wright TJ, Dauwerse HG, Gruter AM, Hofker MH, Moerer P, Williamson R, et al. Wijmenga C, et al. Among authors: hofker mh. Nat Genet. 1992 Sep;2(1):26-30. doi: 10.1038/ng0992-26. Nat Genet. 1992. PMID: 1363881

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