Hoovers JM - Search Results

1

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: hoovers jm. Eur J Hum Genet. 1994;2(1):3-23. doi: 10.1159/000472337. Eur J Hum Genet. 1994. PMID: 7913866

2

Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumors.

Mannens M, Alders M, Redeker B, Bliek J, Steenman M, Wiesmeyer C, de Meulemeester M, Ryan A, Kalikin L, Voûte T, De Kraker J, Hoovers J, Slater R, Feinberg A, Little P, Westerveld A. Mannens M, et al. Med Pediatr Oncol. 1996 Nov;27(5):490-4. doi: 10.1002/(SICI)1096-911X(199611)27:5<490::AID-MPO17>3.0.CO;2-E. Med Pediatr Oncol. 1996. PMID: 8827079 Review.

3

Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments.

Hoovers JM, Kalikin LM, Johnson LA, Alders M, Redeker B, Law DJ, Bliek J, Steenman M, Benedict M, Wiegant J, Lengauer C, Taillon-Miller P, Schlessinger D, Edwards MC, Elledge SJ, Ivens A, Westerveld A, Little P, Mannens M, Feinberg AP. Hoovers JM, et al. Proc Natl Acad Sci U S A. 1995 Dec 19;92(26):12456-60. doi: 10.1073/pnas.92.26.12456. Proc Natl Acad Sci U S A. 1995. PMID: 8618920 Free PMC article.

4

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. Among authors: hoovers jm. Cytogenet Cell Genet. 1995;68(3-4):222-5. doi: 10.1159/000133917. Cytogenet Cell Genet. 1995. PMID: 7842740

5

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. Among authors: hoovers jm. Genomics. 1994 Jun;21(3):538-50. doi: 10.1006/geno.1994.1312. Genomics. 1994. PMID: 7959730 Free article.

6

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: hoovers jm. Genomics. 1991 Oct;11(2):284-93. doi: 10.1016/0888-7543(91)90134-z. Genomics. 1991. PMID: 1769647

7

Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch family.

Mannens M, Bleeker-Wagemakers EM, Bliek J, Hoovers J, Mandjes I, van Tol S, Frants RR, Heyting C, Westerveld A, Slater RM. Mannens M, et al. Cytogenet Cell Genet. 1989;52(1-2):32-6. doi: 10.1159/000132834. Cytogenet Cell Genet. 1989. PMID: 2575483

8

Detection of a cryptic paracentric inversion within band 11p13 in familial aniridia by fluorescence in situ hybridization.

Fukushima Y, Hoovers J, Mannens M, Wakui K, Ohashi H, Ohno T, Ueoka Y, Niikawa N. Fukushima Y, et al. Hum Genet. 1993 Apr;91(3):205-9. doi: 10.1007/BF00218257. Hum Genet. 1993. PMID: 8478003

9

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. Genomics. 1993 Mar;15(3):525-9. doi: 10.1006/geno.1993.1104. Genomics. 1993. PMID: 8468047

10

Further delineation of the partial proximal trisomy 10q syndrome.

Aalfs CM, Hoovers JM, Nieste-Otter MA, Mannens MM, Hennekam RC, Leschot NJ. Aalfs CM, et al. Among authors: hoovers jm. J Med Genet. 1995 Dec;32(12):968-71. doi: 10.1136/jmg.32.12.968. J Med Genet. 1995. PMID: 8825926 Free PMC article.

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