Brunner HG - Search Results

1

Aicardi-Goutières syndrome displays genetic heterogeneity with one locus (AGS1) on chromosome 3p21.

Crow YJ, Jackson AP, Roberts E, van Beusekom E, Barth P, Corry P, Ferrie CD, Hamel BC, Jayatunga R, Karbani G, Kálmánchey R, Kelemen A, King M, Kumar R, Livingstone J, Massey R, McWilliam R, Meager A, Rittey C, Stephenson JB, Tolmie JL, Verrips A, Voit T, van Bokhoven H, Brunner HG, Woods CG. Crow YJ, et al. Among authors: brunner hg. Am J Hum Genet. 2000 Jul;67(1):213-21. doi: 10.1086/302955. Epub 2000 May 25. Am J Hum Genet. 2000. PMID: 10827106 Free PMC article.

2

Intestinal pseudo-obstruction in myotonic dystrophy.

Brunner HG, Hamel BC, Rieu P, Höweler CJ, Peters FT. Brunner HG, et al. J Med Genet. 1992 Nov;29(11):791-3. doi: 10.1136/jmg.29.11.791. J Med Genet. 1992. PMID: 1453429 Free PMC article.

3

Craniofrontonasal dysplasia.

Kapusta L, Brunner HG, Hamel BC. Kapusta L, et al. Among authors: brunner hg. Eur J Pediatr. 1992 Nov;151(11):837-41. doi: 10.1007/BF01957936. Eur J Pediatr. 1992. PMID: 1468459

4

Linkage analysis in X-linked adrenoleukodystrophy and application in post- and prenatal diagnosis.

van Oost BA, van Zandvoort PM, Tünte W, Brunner HG, Hoogeboom AJ, Maaswinkel-Mooy PD, Bakkeren J, Hamel B, Ropers HH. van Oost BA, et al. Among authors: brunner hg. Hum Genet. 1991 Feb;86(4):404-7. doi: 10.1007/BF00201845. Hum Genet. 1991. PMID: 1671851

5

Acrocallosal syndrome.

Hendriks HJ, Brunner HG, Haagen TA, Hamel BC. Hendriks HJ, et al. Among authors: brunner hg. Am J Med Genet. 1990 Mar;35(3):443-6. doi: 10.1002/ajmg.1320350325. Am J Med Genet. 1990. PMID: 2309796

6

Definition of subchromosomal intervals around the myotonic dystrophy locus at 19q.

Brunner H, Coerwinkel-Driessen M, Smeets B, Schonk D, Schepens J, Oerlemans F, Hamel B, Ropers H, Wieringa B. Brunner H, et al. Prog Clin Biol Res. 1989;306:107-14. Prog Clin Biol Res. 1989. PMID: 2740406 No abstract available.

7

Autosomal recessive Melnick-Needles syndrome or ter Haar syndrome? Report of a patient and reappraisal of an earlier report.

Hamel BC, Draaisma JM, Pinckers AJ, Boetes C, Hoppe RL, Ropers HH, Brunner HG. Hamel BC, et al. Among authors: brunner hg. Am J Med Genet. 1995 Apr 10;56(3):312-6. doi: 10.1002/ajmg.1320560320. Am J Med Genet. 1995. PMID: 7778598 Free article. Review.

8

Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM).

Brunner HG, Brüggenwirth HT, Nillesen W, Jansen G, Hamel BC, Hoppe RL, de Die CE, Höweler CJ, van Oost BA, Wieringa B, et al. Brunner HG, et al. Am J Hum Genet. 1993 Nov;53(5):1016-23. Am J Hum Genet. 1993. PMID: 8213829 Free PMC article.

9

Exclusion of the neurofibromatosis 1 locus in a family with inherited café-au-lait spots.

Brunner HG, Hulsebos T, Steijlen PM, der Kinderen DJ, vd Steen A, Hamel BC. Brunner HG, et al. Am J Med Genet. 1993 Jun 1;46(4):472-4. doi: 10.1002/ajmg.1320460428. Am J Med Genet. 1993. PMID: 8357027

10

Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13.

Gong Y, Vikkula M, Boon L, Liu J, Beighton P, Ramesar R, Peltonen L, Somer H, Hirose T, Dallapiccola B, De Paepe A, Swoboda W, Zabel B, Superti-Furga A, Steinmann B, Brunner HG, Jans A, Boles RG, Adkins W, van den Boogaard MJ, Olsen BR, Warman ML. Gong Y, et al. Among authors: brunner hg. Am J Hum Genet. 1996 Jul;59(1):146-51. Am J Hum Genet. 1996. PMID: 8659519 Free PMC article.

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