| Unbound MEDLINE results for: | Bookmark this site | | Articles related to 18505544 [Unique ID], provided by the PubMed system | |
| |
|
| | 1 - 10 of 113 journal articles in the PubMed database | Email to a friend | | |
| Sarkozy A, Digilio MC, Dallapiccola B
LEOPARD syndrome. [JOURNAL ARTICLE]
Orphanet J Rare Dis 2008 May 27; 3(1):13.
Abstract | Full Citation | Find Related Articles | | Digilio MC, Sarkozy A, de Zorzi A, et al.
LEOPARD syndrome: clinical diagnosis in the first year of life. [Journal Article]
Am J Med Genet A 2006 Apr 1; 140(7):740-6.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Digilio MC, Conti E, Sarkozy A, et al.
Grouping of multiple-lentigines/LEOPARD and Noonan syndromes on the PTPN11 gene. [Journal Article]
Am J Hum Genet 2002 Aug; 71(2):389-94.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Paradisi M, Pedicelli C, Ciasulli A, et al.
[PTPN11 gene mutation in LEOPARD syndrome] [Case Reports, Journal Article]
Minerva Pediatr 2005 Aug; 57(4):189-93.
Abstract | Full Citation | Find Related Articles | | Digilio MC, Pacileo G, Sarkozy A, et al.
Familial aggregation of genetically heterogeneous hypertrophic cardiomyopathy: a boy with LEOPARD syndrome due to PTPN11 mutation and his nonsyndromic father lacking PTPN11 mutations. [Case Reports, Journal Article]
Birth Defects Res A Clin Mol Teratol 2004 Feb; 70(2):95-8.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Digilio MC, Sarkozy A, Pacileo G, et al.
PTPN11 gene mutations: linking the Gln510Glu mutation to the "LEOPARD syndrome phenotype" [JOURNAL ARTICLE]
Eur J Pediatr 2006 May 30.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | van der Burgt I
Noonan syndrome. [JOURNAL ARTICLE]
Orphanet J Rare Dis 2007 Jan 14; 2(1):4.
Abstract | Full Citation | Find Related Articles | | Porciello R, Divona L, Strano S, et al.
Leopard syndrome. [Journal Article]
Dermatol Online J 2008; 14(3):7.
Abstract | Full Citation | Find Related Articles | | Legius E, Schrander-Stumpel C, Schollen E, et al.
PTPN11 mutations in LEOPARD syndrome. [Case Reports, Journal Article]
J Med Genet 2002 Aug; 39(8):571-4.
Abstract | Full Citation | Publisher Full Text | Find Related Articles |   |
|
| |
Advertise on this site.
|
