Dumanski J - Search Results

1

Mutations in short stature homeobox containing gene (SHOX) in dyschondrosteosis but not in hypochondroplasia.

Grigelioniene G, Eklöf O, Ivarsson SA, Westphal O, Neumeyer L, Kedra D, Dumanski J, Hagenäs L. Grigelioniene G, et al. Among authors: dumanski j. Hum Genet. 2000 Aug;107(2):145-9. doi: 10.1007/s004390000352. Hum Genet. 2000. PMID: 11030412

2

Analysis of short stature homeobox-containing gene ( SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity.

Grigelioniene G, Schoumans J, Neumeyer L, Ivarsson A, Eklöf O, Enkvist O, Tordai P, Fosdal I, Myhre AG, Westphal O, Nilsson NO, Elfving M, Ellis I, Anderlid BM, Fransson I, Tapia-Paez I, Nordenskjöld M, Hagenäs L, Dumanski JP. Grigelioniene G, et al. Among authors: dumanski jp. Hum Genet. 2001 Nov;109(5):551-8. doi: 10.1007/s00439-001-0609-y. Epub 2001 Oct 19. Hum Genet. 2001. PMID: 11735031

3

Asn540Lys mutation in fibroblast growth factor receptor 3 and phenotype in hypochondroplasia.

Grigelioniené G, Eklöf O, Laurencikas E, Ollars B, Hertel NT, Dumanski JP, Hagenäs L. Grigelioniené G, et al. Among authors: dumanski jp. Acta Paediatr. 2000 Sep;89(9):1072-6. doi: 10.1080/713794579. Acta Paediatr. 2000. PMID: 11071087

4

Characterization of a second human clathrin heavy chain polypeptide gene (CLH-22) from chromosome 22q11.

Kedra D, Peyrard M, Fransson I, Collins JE, Dunham I, Roe BA, Dumanski JP. Kedra D, et al. Among authors: dumanski jp. Hum Mol Genet. 1996 May;5(5):625-31. doi: 10.1093/hmg/5.5.625. Hum Mol Genet. 1996. PMID: 8733129

5

Characterization of the human synaptogyrin gene family.

Kedra D, Pan HQ, Seroussi E, Fransson I, Guilbaud C, Collins JE, Dunham I, Blennow E, Roe BA, Piehl F, Dumanski JP. Kedra D, et al. Among authors: dumanski jp. Hum Genet. 1998 Aug;103(2):131-41. doi: 10.1007/s004390050795. Hum Genet. 1998. PMID: 9760194

6

A novel gene containing LIM domains (LIMD1) is located within the common eliminated region 1 (C3CER1) in 3p21.3.

Kiss H, Kedra D, Yang Y, Kost-Alimova M, Kiss C, O'Brien KP, Fransson I, Klein G, Imreh S, Dumanski JP. Kiss H, et al. Among authors: dumanski jp. Hum Genet. 1999 Dec;105(6):552-9. doi: 10.1007/s004399900188. Hum Genet. 1999. PMID: 10647888

7

Fine mapping of the constitutional translocation t(11;22)(q23;q11).

Tapia-Páez I, O'Brien KP, Kost-Alimova M, Sahlén S, Kedra D, Bruder CE, Andersson B, Roe BA, Hu P, Imreh S, Blennow E, Dumanski JP. Tapia-Páez I, et al. Among authors: dumanski jp. Hum Genet. 2000 May;106(5):506-16. doi: 10.1007/s004390000287. Hum Genet. 2000. PMID: 10914680

8

The germinal center kinase gene and a novel CDC25-like gene are located in the vicinity of the PYGM gene on 11q13.

Kedra D, Seroussi E, Fransson I, Trifunovic J, Clark M, Lagercrantz J, Blennow E, Mehlin H, Dumanski J. Kedra D, et al. Among authors: dumanski j. Hum Genet. 1997 Oct;100(5-6):611-9. doi: 10.1007/s004390050562. Hum Genet. 1997. PMID: 9341881

9

Characterization of the human NIPSNAP1 gene from 22q12: a member of a novel gene family.

Seroussi E, Pan HQ, Kedra D, Roe BA, Dumanski JP. Seroussi E, et al. Among authors: dumanski jp. Gene. 1998 May 28;212(1):13-20. doi: 10.1016/s0378-1119(98)00098-5. Gene. 1998. PMID: 9661659

10

The mouse ortholog of the human SMARCB1 gene encodes two splice forms.

Bruder CE, Dumanski JP, Kedra D. Bruder CE, et al. Among authors: dumanski jp. Biochem Biophys Res Commun. 1999 Apr 21;257(3):886-90. doi: 10.1006/bbrc.1999.0563. Biochem Biophys Res Commun. 1999. PMID: 10208879

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

161 results

Search Page

Filters