Frants RR - Search Results

1

Facioscapulohumeral muscular dystrophy gene in Dutch families is not linked to markers for familial adenomatous polyposis on the long arm of chromosome 5.

Wijmenga C, Frants RR, Brouwer OF, van der Klift HM, Meera Khan P, Padberg GW. Wijmenga C, et al. Among authors: frants rr. J Neurol Sci. 1990 Feb;95(2):225-9. doi: 10.1016/0022-510x(90)90245-i. J Neurol Sci. 1990. PMID: 2157824

2

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: frants rr. Muscle Nerve Suppl. 1995;2:S19-26. Muscle Nerve Suppl. 1995. PMID: 7739621 Free article.

3

The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qter.

Bakker E, Wijmenga C, Vossen RH, Padberg GW, Hewitt J, van der Wielen M, Rasmussen K, Frants RR. Bakker E, et al. Among authors: frants rr. Muscle Nerve Suppl. 1995;2:S39-44. Muscle Nerve Suppl. 1995. PMID: 7739624 Free article.

4

Early onset facioscapulohumeral muscular dystrophy.

Brouwer OF, Padberg GW, Bakker E, Wijmenga C, Frants RR. Brouwer OF, et al. Among authors: frants rr. Muscle Nerve Suppl. 1995;2:S67-72. Muscle Nerve Suppl. 1995. PMID: 7739629

5

On the significance of retinal vascular disease and hearing loss in facioscapulohumeral muscular dystrophy.

Padberg GW, Brouwer OF, de Keizer RJ, Dijkman G, Wijmenga C, Grote JJ, Frants RR. Padberg GW, et al. Among authors: frants rr. Muscle Nerve Suppl. 1995;2:S73-80. Muscle Nerve Suppl. 1995. PMID: 7739630 Free article.

6

Facioscapulohumeral muscular dystrophy in the Dutch population.

Padberg GW, Frants RR, Brouwer OF, Wijmenga C, Bakker E, Sandkuijl LA. Padberg GW, et al. Among authors: frants rr. Muscle Nerve Suppl. 1995;2:S81-4. Muscle Nerve Suppl. 1995. PMID: 7739631 Free article.

7

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: frants rr. Genomics. 1994 Jan 1;19(1):21-6. doi: 10.1006/geno.1994.1006. Genomics. 1994. PMID: 7910579

8

Facioscapulohumeral muscular dystrophy: the impact of genetic research.

Brouwer OF, Wijmenga C, Frants RR, Padberg GW. Brouwer OF, et al. Among authors: frants rr. Clin Neurol Neurosurg. 1993 Mar;95(1):9-21. doi: 10.1016/0303-8467(93)90086-v. Clin Neurol Neurosurg. 1993. PMID: 8095870 Review.

9

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: frants rr. Hum Genet. 1993 Sep;92(2):198-203. doi: 10.1007/BF00219692. Hum Genet. 1993. PMID: 8103757

10

Genetic mapping of facioscapulohumeral muscular dystrophy.

Wijmenga C, Hofker MH, Padberg GW, Frants RR. Wijmenga C, et al. Among authors: frants rr. 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.

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