Similar articles for PMID: 11185075

Year	Number of Results
1990	1
1992	3
1993	5
1994	2
1996	3
1997	4
1998	3
1999	4
2000	6
2001	3
2002	6
2003	4
2004	3
2005	5
2006	7
2007	7
2008	3
2009	4
2010	1
2012	1
2013	1
2014	1
2015	3
2016	2
2017	2
2020	1
2024	0

1

Detailed mapping, mutation analysis, and intragenic polymorphism identification in candidate Noonan syndrome genes MYL2, DCN, EPS8, and RPL6.

Ion A, Crosby AH, Kremer H, Kenmochi N, Van Reen M, Fenske C, Van Der Burgt I, Brunner HG, Montgomery K, Kucherlapati RS, Patton MA, Page C, Mariman E, Jeffery S. Ion A, et al. J Med Genet. 2000 Nov;37(11):884-6. doi: 10.1136/jmg.37.11.884. J Med Genet. 2000. PMID: 11185075 Free PMC article. No abstract available.

2

The human ribosomal protein L6 gene in a critical region for Noonan syndrome.

Kenmochi N, Yoshihama M, Higa S, Tanaka T. Kenmochi N, et al. J Hum Genet. 2000;45(5):290-3. doi: 10.1007/s100380070018. J Hum Genet. 2000. PMID: 11043511

3

Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy.

Flavigny J, Richard P, Isnard R, Carrier L, Charron P, Bonne G, Forissier JF, Desnos M, Dubourg O, Komajda M, Schwartz K, Hainque B. Flavigny J, et al. J Mol Med (Berl). 1998 Mar;76(3-4):208-14. doi: 10.1007/s001090050210. J Mol Med (Berl). 1998. PMID: 9535554

4

Assignment of keratocan gene (KERA) to human chromosome band 12q22 by in situ hybridization.

Tasheva ES, Pettenati M, Von Kap-Her C, Conrad GW. Tasheva ES, et al. Cytogenet Cell Genet. 2000;88(3-4):244-5. doi: 10.1159/000015528. Cytogenet Cell Genet. 2000. PMID: 10828599 No abstract available.

5

Localization of PGI (biglycan, BGN) and PGII (decorin, DCN, PG-40) genes on human chromosomes Xq13-qter and 12q, respectively.

McBride OW, Fisher LW, Young MF. McBride OW, et al. Genomics. 1990 Feb;6(2):219-25. doi: 10.1016/0888-7543(90)90560-h. Genomics. 1990. PMID: 1968422

6

Length polymorphism within a complex dinucleotide repeat in the human decorin (DCN) gene.

Briggs MD, Cohn DH. Briggs MD, et al. Hum Mol Genet. 1993 Jul;2(7):1087. doi: 10.1093/hmg/2.7.1087-a. Hum Mol Genet. 1993. PMID: 8364565 No abstract available.

7

Chromosomal localization, genomic characterization, and mapping to the Noonan syndrome critical region of the human Deltex (DTX1) gene.

Lee L, Dowhanick-Morrissette J, Katz A, Jukofsky L, Krantz ID. Lee L, et al. Hum Genet. 2000 Dec;107(6):577-81. doi: 10.1007/s004390000431. Hum Genet. 2000. PMID: 11153911

8

PTPN11 mutation in a large family with Noonan syndrome and dizygous twinning.

Schollen E, Matthijs G, Gewillig M, Fryns JP, Legius E. Schollen E, et al. Eur J Hum Genet. 2003 Jan;11(1):85-8. doi: 10.1038/sj.ejhg.5200915. Eur J Hum Genet. 2003. PMID: 12529711

9

Molecular characterization of a balanced rearrangement of chromosome 12 in two siblings with Noonan syndrome.

Yatsenko SA, del Valle Torrado M, Fernandes PH, Wiszniewska J, Gallego M, Herrera J, Bacino CA. Yatsenko SA, et al. Am J Med Genet A. 2009 Dec;149A(12):2723-30. doi: 10.1002/ajmg.a.33112. Am J Med Genet A. 2009. PMID: 19938085

10

Further delineation of the critical region for noonan syndrome on the long arm of chromosome 12.

Brady AF, Jamieson CR, van der Burgt I, Crosby A, van Reen M, Kremer H, Mariman E, Patton MA, Jeffery S. Brady AF, et al. Eur J Hum Genet. 1997 Sep-Oct;5(5):336-7. Eur J Hum Genet. 1997. PMID: 9412792 No abstract available.

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 NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

78 results

Results by year