Vazquez MP - Search Results

1

The Beckwith-Wiedemann syndrome phenotype and the risk of cancer.

Schneid H, Vazquez MP, Vacher C, Gourmelen M, Cabrol S, Le Bouc Y. Schneid H, et al. Among authors: vazquez mp. Med Pediatr Oncol. 1997 Jun;28(6):411-5. doi: 10.1002/(sici)1096-911x(199706)28:6<411::aid-mpo3>3.0.co;2-j. Med Pediatr Oncol. 1997. PMID: 9143384

2

Loss of heterozygosity in non-tumoral tissue in two children with Beckwith-Wiedemann syndrome.

Schneid H, Vazquez MP, Seurin D, le Bouc Y. Schneid H, et al. Among authors: vazquez mp. Growth Regul. 1991 Dec;1(4):168-70. Growth Regul. 1991. PMID: 1688177

3

[Wiedemann-Beckwith syndrome: apropos of 20 cases].

Vacher C, Vazquez MP, Le Bouc Y, Schneid H. Vacher C, et al. Among authors: vazquez mp. Rev Stomatol Chir Maxillofac. 1994;95(2):192-3. Rev Stomatol Chir Maxillofac. 1994. PMID: 8036428 French. No abstract available.

4

Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome.

Schneid H, Seurin D, Vazquez MP, Gourmelen M, Cabrol S, Le Bouc Y. Schneid H, et al. Among authors: vazquez mp. J Med Genet. 1993 May;30(5):353-62. doi: 10.1136/jmg.30.5.353. J Med Genet. 1993. PMID: 8320696 Free PMC article.

5

Assessment of p57(KIP2) gene mutation in Beckwith-Wiedemann syndrome.

Gaston V, Le Bouc Y, Soupre V, Vazquez MP, Gicquel C. Gaston V, et al. Among authors: vazquez mp. Horm Res. 2000;54(1):1-5. doi: 10.1159/000063429. Horm Res. 2000. PMID: 11182628

6

Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome.

Gaston V, Le Bouc Y, Soupre V, Burglen L, Donadieu J, Oro H, Audry G, Vazquez MP, Gicquel C. Gaston V, et al. Among authors: vazquez mp. Eur J Hum Genet. 2001 Jun;9(6):409-18. doi: 10.1038/sj.ejhg.5200649. Eur J Hum Genet. 2001. PMID: 11436121

7

[The Wiedemann-Beckwith syndrome and a congenital cataract].

Momtchilova M, Pelosse B, Laroche L, Vazquez MP. Momtchilova M, et al. Among authors: vazquez mp. J Fr Ophtalmol. 2001 May;24(5):479-81. J Fr Ophtalmol. 2001. PMID: 11397983 French.

8

Linkage analysis of 5 novel van der Woude syndrome kindreds to 1q32-q41 markers further supports locus homogeneity of the disease trait.

Houdayer C, Soupre V, Rosenberg-Bourgin M, Martinez H, Tredano M, Feldmann D, Feingold J, Aymard P, Munnich A, Le Bouc Y, Vazquez MP, Bahuau M. Houdayer C, et al. Among authors: vazquez mp. Ann Genet. 1999;42(2):69-74. Ann Genet. 1999. PMID: 10434119

9

Beckwith-Wiedemann-like macroglossia and 18q23 haploinsufficiency.

Lirussi F, Jonard L, Gaston V, Sanlaville D, Kooy RF, Winnepenninckx B, Maher ER, Fitzpatrick DR, Gicquel C, Portnoï MF, Couderc R, Vazquez MP, Bahuau M. Lirussi F, et al. Among authors: vazquez mp. Am J Med Genet A. 2007 Dec 1;143A(23):2796-803. doi: 10.1002/ajmg.a.31768. Am J Med Genet A. 2007. PMID: 17994567

10

1q32-q41 microdeletion with reference to Van der Woude syndrome and allied clefting entities.

Houdayer C, Soupre V, Karcenty B, Vazquez MP, Odent S, Lacombe D, Le Bouc Y, Munnich A, Bahuau M. Houdayer C, et al. Among authors: vazquez mp. Am J Med Genet. 2000 Mar 13;91(2):161-3. doi: 10.1002/(sici)1096-8628(20000313)91:2<161::aid-ajmg18>3.0.co;2-q. Am J Med Genet. 2000. PMID: 10748420 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

Text availability

Article attribute

Article type

Publication date

163 results

Search Page