Kunz J - Search Results

1

A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1.

Johnson D, Horsley SW, Moloney DM, Oldridge M, Twigg SR, Walsh S, Barrow M, Njølstad PR, Kunz J, Ashworth GJ, Wall SA, Kearney L, Wilkie AO. Johnson D, et al. Among authors: kunz j. Am J Hum Genet. 1998 Nov;63(5):1282-93. doi: 10.1086/302122. Am J Hum Genet. 1998. PMID: 9792856 Free PMC article.

2

Translocation breakpoint maps 5 kb 3' from TWIST in a patient affected with Saethre-Chotzen syndrome.

Krebs I, Weis I, Hudler M, Rommens JM, Roth H, Scherer SW, Tsui LC, Füchtbauer EM, Grzeschik KH, Tsuji K, Kunz J. Krebs I, et al. Among authors: kunz j. Hum Mol Genet. 1997 Jul;6(7):1079-86. doi: 10.1093/hmg/6.7.1079. Hum Mol Genet. 1997. PMID: 9215678

3

Saethre-Chotzen syndrome and hyper IgE syndrome in a patient with a novel 11 bp deletion of the TWIST gene.

Boeck A, Kosan C, Ciznar P, Kunz J. Boeck A, et al. Among authors: kunz j. Am J Med Genet. 2001 Nov 15;104(1):53-6. doi: 10.1002/ajmg.10007. Am J Med Genet. 2001. PMID: 11746028

4

Six new polymorphic microsatellite markers used for the integration of genetic and physical maps of human chromosome 7.

Beck S, Badbanchi F, Otto M, Grzeschik N, Kunz J, Speich N, Gessler M, Grzeschik KH. Beck S, et al. Among authors: kunz j. Hum Genet. 1996 Jun;97(6):842-4. doi: 10.1007/BF02346201. Hum Genet. 1996. PMID: 8641708

5

The breakpoint on 7p in a patient with t(6;7) and craniosynostosis is spanned by a YAC clone containing the D7S503 locus.

Tsuji K, Narahara K, Yokoyama Y, Grzeschik KH, Kunz J. Tsuji K, et al. Among authors: kunz j. Hum Genet. 1995 Mar;95(3):303-7. doi: 10.1007/BF00225198. Hum Genet. 1995. PMID: 7868123

6

A solitary human H3 histone gene on chromosome 1.

Albig W, Ebentheuer J, Klobeck G, Kunz J, Doenecke D. Albig W, et al. Among authors: kunz j. Hum Genet. 1996 Apr;97(4):486-91. doi: 10.1007/BF02267072. Hum Genet. 1996. PMID: 8834248

7

Phenotypic findings due to trisomy 7p15.3-pter including the TWIST locus.

Stankiewicz P, Thiele H, Baldermann C, Krüger A, Giannakudis I, Dörr S, Werner N, Kunz J, Rappold GA, Hansmann I. Stankiewicz P, et al. Among authors: kunz j. Am J Med Genet. 2001 Sep 15;103(1):56-62. doi: 10.1002/ajmg.1512. Am J Med Genet. 2001. PMID: 11562935 Review.

8

Saethre-Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome.

Kress W, Schropp C, Lieb G, Petersen B, Büsse-Ratzka M, Kunz J, Reinhart E, Schäfer WD, Sold J, Hoppe F, Pahnke J, Trusen A, Sörensen N, Krauss J, Collmann H. Kress W, et al. Among authors: kunz j. Eur J Hum Genet. 2006 Jan;14(1):39-48. doi: 10.1038/sj.ejhg.5201507. Eur J Hum Genet. 2006. PMID: 16251895

9

Transmission disequilibrium and sequence variants at the leptin receptor gene in extremely obese German children and adolescents.

Roth H, Korn T, Rosenkranz K, Hinney A, Ziegler A, Kunz J, Siegfried W, Mayer H, Hebebrand J, Grzeschik KH. Roth H, et al. Among authors: kunz j. Hum Genet. 1998 Nov;103(5):540-6. doi: 10.1007/s004390050867. Hum Genet. 1998. PMID: 9860295

10

Identification and characterisation of the gene TWIST NEIGHBOR (TWISTNB) located in the microdeletion syndrome 7p21 region.

Kosan C, Kunz J. Kosan C, et al. Among authors: kunz j. Cytogenet Genome Res. 2002;97(3-4):167-70. doi: 10.1159/000066618. Cytogenet Genome Res. 2002. PMID: 12438708

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