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Feingold syndrome: clinical review and genetic mapping.
Celli J, van Bokhoven H, Brunner HG. Celli J, et al. Among authors: brunner hg. Am J Med Genet A. 2003 Nov 1;122A(4):294-300. doi: 10.1002/ajmg.a.20471. Am J Med Genet A. 2003. PMID: 14518066 Review.
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
Two additional cases of the Ohdo blepharophimosis syndrome.
Maat-Kievit A, Brunner HG, Maaswinkel-Mooij P. Maat-Kievit A, et al. Among authors: brunner hg. Am J Med Genet. 1993 Nov 1;47(6):901-6. doi: 10.1002/ajmg.1320470618. Am J Med Genet. 1993. PMID: 8279489 Review.
Assignment of WNT7B to human chromosome band 22q13 by in situ hybridization.
van Bokhoven H, Kissing J, Schepens M, van Beersum S, Simons A, Riegman P, McMahon JA, McMahon AP, Brunner HG. van Bokhoven H, et al. Among authors: brunner hg. Cytogenet Cell Genet. 1997;77(3-4):288-9. doi: 10.1159/000134600. Cytogenet Cell Genet. 1997. PMID: 9284940 Free article. No abstract available.
Limb mammary syndrome: a new genetic disorder with mammary hypoplasia, ectrodactyly, and other Hand/Foot anomalies maps to human chromosome 3q27.
van Bokhoven H, Jung M, Smits AP, van Beersum S, Rüschendorf F, van Steensel M, Veenstra M, Tuerlings JH, Mariman EC, Brunner HG, Wienker TF, Reis A, Ropers HH, Hamel BC. van Bokhoven H, et al. Among authors: brunner hg. Am J Hum Genet. 1999 Feb;64(2):538-46. doi: 10.1086/302246. Am J Hum Genet. 1999. PMID: 9973291 Free PMC article.
491 results