Redeker E - Search Results

1

An integrated physical map of 210 markers assigned to the short arm of human chromosome 11.

Redeker E, Hoovers JM, Alders M, van Moorsel CJ, Ivens AC, Gregory S, Kalikin L, Bliek J, de Galan L, van den Bogaard R, et al. Redeker E, et al. Genomics. 1994 Jun;21(3):538-50. doi: 10.1006/geno.1994.1312. Genomics. 1994. PMID: 7959730 Free article.

2

The distal region of 11p13 and associated genetic diseases.

Mannens M, Hoovers JM, Bleeker-Wagemakers EM, Redeker E, Bliek J, Overbeeke-Melkert M, Saunders G, Williams B, van Heyningen V, Junien C, et al. Mannens M, et al. Among authors: redeker e. Genomics. 1991 Oct;11(2):284-93. doi: 10.1016/0888-7543(91)90134-z. Genomics. 1991. PMID: 1769647

3

Physical mapping of 3 candidate tumor suppressor genes relative to Beckwith-Wiedemann syndrome associated chromosomal breakpoints at 11p15.3.

Redeker E, Alders M, Hoovers JM, Richard CW 3rd, Westerveld A, Mannens M. Redeker E, et al. Cytogenet Cell Genet. 1995;68(3-4):222-5. doi: 10.1159/000133917. Cytogenet Cell Genet. 1995. PMID: 7842740

4

Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia.

Mannens M, Hoovers JM, Redeker E, Verjaal M, Feinberg AP, Little P, Boavida M, Coad N, Steenman M, Bliek J, et al. Mannens M, et al. Among authors: redeker e. Eur J Hum Genet. 1994;2(1):3-23. doi: 10.1159/000472337. Eur J Hum Genet. 1994. PMID: 7913866

5

High-resolution chromosomal localization of the human calcitonin/CGRP/IAPP gene family members.

Hoovers JM, Redeker E, Speleman F, Höppener JW, Bhola S, Bliek J, van Roy N, Leschot NJ, Westerveld A, Mannens M. Hoovers JM, et al. Among authors: redeker e. Genomics. 1993 Mar;15(3):525-9. doi: 10.1006/geno.1993.1104. Genomics. 1993. PMID: 8468047

6

TaqI and RsaI polymorphisms in the H19 gene (D11S813E).

Redeker E, Van Moorsel CJ, Feinberg A, Mannens M. Redeker E, et al. Hum Mol Genet. 1993 Jun;2(6):823. doi: 10.1093/hmg/2.6.823. Hum Mol Genet. 1993. PMID: 8102574 No abstract available.

7

Prospective screening for subtelomeric rearrangements in children with mental retardation of unknown aetiology: the Amsterdam experience.

van Karnebeek CD, Koevoets C, Sluijter S, Bijlsma EK, Smeets DF, Redeker EJ, Hennekam RC, Hoovers JM. van Karnebeek CD, et al. Among authors: redeker ej. J Med Genet. 2002 Aug;39(8):546-53. doi: 10.1136/jmg.39.8.546. J Med Genet. 2002. PMID: 12161591 Free PMC article.

8

An aetiological study of 25 mentally retarded adults with autism.

van Karnebeek CD, van Gelderen I, Nijhof GJ, Abeling NG, Vreken P, Redeker EJ, van Eeghen AM, Hoovers JM, Hennekam RC. van Karnebeek CD, et al. Among authors: redeker ej. J Med Genet. 2002 Mar;39(3):205-13. doi: 10.1136/jmg.39.3.205. J Med Genet. 2002. PMID: 11897827 Free PMC article. No abstract available.

9

Whole-exome sequencing is a powerful approach for establishing the etiological diagnosis in patients with intellectual disability and microcephaly.

Rump P, Jazayeri O, van Dijk-Bos KK, Johansson LF, van Essen AJ, Verheij JB, Veenstra-Knol HE, Redeker EJ, Mannens MM, Swertz MA, Alizadeh BZ, van Ravenswaaij-Arts CM, Sinke RJ, Sikkema-Raddatz B. Rump P, et al. Among authors: redeker ej. BMC Med Genomics. 2016 Feb 4;9:7. doi: 10.1186/s12920-016-0167-8. BMC Med Genomics. 2016. PMID: 26846091 Free PMC article.

10

DNA diagnosis in a family with autosomal dominant aniridia.

Verbraak FD, Mannens MA, Redeker EJ, Saunders GF, Bleeker-Wagemakers EM. Verbraak FD, et al. Among authors: redeker ej. Ophthalmic Paediatr Genet. 1991 Dec;12(4):165-70. doi: 10.3109/13816819109025812. Ophthalmic Paediatr Genet. 1991. PMID: 1815167

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