Bakker E - Search Results

1

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. Muscle Nerve Suppl. 1995;(2):S39-44. Muscle Nerve Suppl. 1995. PMID: 23573585

2

Somatic mosaicism in FSHD often goes undetected.

Lemmers RJ, van der Wielen MJ, Bakker E, Padberg GW, Frants RR, van der Maarel SM. Lemmers RJ, et al. Among authors: bakker e. Ann Neurol. 2004 Jun;55(6):845-50. doi: 10.1002/ana.20106. Ann Neurol. 2004. PMID: 15174019

3

Early onset facioscapulohumeral muscular dystrophy.

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

4

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: bakker e. Muscle Nerve Suppl. 1995;2:S81-4. Muscle Nerve Suppl. 1995. PMID: 7739631 Free article.

5

Diagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: diagnostic approach for sporadic and familial cases.

Bakker E, Van der Wielen MJ, Voorhoeve E, Ippel PF, Padberg GW, Frants RR, Wijmenga C. Bakker E, et al. J Med Genet. 1996 Jan;33(1):29-35. doi: 10.1136/jmg.33.1.29. J Med Genet. 1996. PMID: 8825045 Free PMC article.

6

Evidence for subtelomeric exchange of 3.3 kb tandemly repeated units between chromosomes 4q35 and 10q26: implications for genetic counselling and etiology of FSHD1.

van Deutekom JC, Bakker E, Lemmers RJ, van der Wielen MJ, Bik E, Hofker MH, Padberg GW, Frants RR. van Deutekom JC, et al. Among authors: bakker e. Hum Mol Genet. 1996 Dec;5(12):1997-2003. doi: 10.1093/hmg/5.12.1997. Hum Mol Genet. 1996. PMID: 8968754

7

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

8

A new dosage test for subtelomeric 4;10 translocations improves conventional diagnosis of facioscapulohumeral muscular dystrophy (FSHD).

van der Maarel SM, Deidda G, Lemmers RJ, Bakker E, van der Wielen MJ, Sandkuijl L, Hewitt JE, Padberg GW, Frants RR. van der Maarel SM, et al. Among authors: bakker e. J Med Genet. 1999 Nov;36(11):823-8. J Med Genet. 1999. PMID: 10544225 Free PMC article.

9

Complete allele information in the diagnosis of facioscapulohumeral muscular dystrophy by triple DNA analysis.

Lemmers RJL, de Kievit P, van Geel M, van der Wielen MJ, Bakker E, Padberg GW, Frants RR, van der Maarel SM. Lemmers RJL, et al. Among authors: bakker e. Ann Neurol. 2001 Dec;50(6):816-9. doi: 10.1002/ana.10057. Ann Neurol. 2001. PMID: 11761483

10

Possible phenotypic dosage effect in patients compound heterozygous for FSHD-sized 4q35 alleles.

Wohlgemuth M, Lemmers RJ, van der Kooi EL, van der Wielen MJ, van Overveld PG, Dauwerse H, Bakker E, Frants RR, Padberg GW, van der Maarel SM. Wohlgemuth M, et al. Among authors: bakker e. Neurology. 2003 Oct 14;61(7):909-13. doi: 10.1212/wnl.61.7.909. Neurology. 2003. PMID: 14557558

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,109 results

Search Page

Filters