Hofker MH - Search Results

1

Molecular genetics of facioscapulohumeral muscular dystrophy.

Wijmenga C, Frants RR, Hewitt JE, van Deutekom JC, van Geel M, Wright TJ, Padberg GW, Hofker MH, van Ommen GJ. Wijmenga C, et al. Among authors: hofker mh. Neuromuscul Disord. 1993 Sep-Nov;3(5-6):487-91. doi: 10.1016/0960-8966(93)90102-p. Neuromuscul Disord. 1993. PMID: 8186699 Review.

2

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. Hum Mol Genet. 1998 Aug;7(8):1207-14. doi: 10.1093/hmg/7.8.1207. Hum Mol Genet. 1998. PMID: 9668160

3

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

4

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.

5

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: 7739621 Free article.

6

Pulsed-field gel electrophoresis of the D4F104S1 locus reveals the size and the parental origin of the facioscapulohumeral muscular dystrophy (FSHD)-associated deletions.

Wijmenga C, van Deutekom JC, Hewitt JE, Padberg GW, van Ommen GJ, Hofker MH, Frants RR. Wijmenga C, et al. Among authors: hofker mh. Genomics. 1994 Jan 1;19(1):21-6. doi: 10.1006/geno.1994.1006. Genomics. 1994. PMID: 7910579

7

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

8

FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit.

van Deutekom JC, Wijmenga C, van Tienhoven EA, Gruter AM, Hewitt JE, Padberg GW, van Ommen GJ, Hofker MH, Frants RR. van Deutekom JC, et al. Among authors: hofker mh. Hum Mol Genet. 1993 Dec;2(12):2037-42. doi: 10.1093/hmg/2.12.2037. Hum Mol Genet. 1993. PMID: 8111371

9

Genetic mapping of facioscapulohumeral muscular dystrophy.

Wijmenga C, Hofker MH, Padberg GW, Frants RR. Wijmenga C, et al. Among authors: hofker mh. Mol Cell Biol Hum Dis Ser. 1993;3:111-38. doi: 10.1007/978-94-011-1528-5_5. Mol Cell Biol Hum Dis Ser. 1993. PMID: 8111536 Review. No abstract available.

10

Physical mapping and YAC-cloning connects four genetically distinct 4qter loci (D4S163, D4S139, D4F35S1 and D4F104S1) in the FSHD gene-region.

Wijmenga C, Wright TJ, Baan MJ, Padberg GW, Williamson R, van Ommen GJ, Hewitt JE, Hofker MH, Frants RR. Wijmenga C, et al. Among authors: hofker mh. Hum Mol Genet. 1993 Oct;2(10):1667-72. doi: 10.1093/hmg/2.10.1667. Hum Mol Genet. 1993. PMID: 8268920

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