Palka G - Search Results

1

Genetics of syndromic and nonsyndromic cleft lip and palate.

Stuppia L, Capogreco M, Marzo G, La Rovere D, Antonucci I, Gatta V, Palka G, Mortellaro C, Tetè S. Stuppia L, et al. Among authors: palka g. J Craniofac Surg. 2011 Sep;22(5):1722-6. doi: 10.1097/SCS.0b013e31822e5e4d. J Craniofac Surg. 2011. PMID: 21959420 Review.

2

Two novel mutations affecting splicing in the IRF6 gene associated with van der Woude syndrome.

Scioletti AP, Brancati F, Gatta V, Antonucci I, Peissel B, Pizzuti A, Mortellaro C, Tetè S, Gherlone E, Palka G, Stuppia L. Scioletti AP, et al. Among authors: palka g. J Craniofac Surg. 2010 Sep;21(5):1654-6. doi: 10.1097/SCS.0b013e3181ef69ef. J Craniofac Surg. 2010. PMID: 20856073

3

Testis transcriptome analysis in male infertility: new insight on the pathogenesis of oligo-azoospermia in cases with and without AZFc microdeletion.

Gatta V, Raicu F, Ferlin A, Antonucci I, Scioletti AP, Garolla A, Palka G, Foresta C, Stuppia L. Gatta V, et al. Among authors: palka g. BMC Genomics. 2010 Jun 24;11:401. doi: 10.1186/1471-2164-11-401. BMC Genomics. 2010. PMID: 20576090 Free PMC article.

4

Use of the MLPA assay in the molecular diagnosis of gene copy number alterations in human genetic diseases.

Stuppia L, Antonucci I, Palka G, Gatta V. Stuppia L, et al. Among authors: palka g. Int J Mol Sci. 2012;13(3):3245-3276. doi: 10.3390/ijms13033245. Epub 2012 Mar 8. Int J Mol Sci. 2012. PMID: 22489151 Free PMC article. Review.

5

Genetic testing in couples undergoing assisted reproduction technique protocols.

Stuppia L, Gatta V, Antonucci I, Giuliani R, Scioletti AP, Palka G. Stuppia L, et al. Among authors: palka g. Expert Opin Med Diagn. 2009 Sep;3(5):571-83. doi: 10.1517/17530050902970986. Epub 2009 Jul 29. Expert Opin Med Diagn. 2009. PMID: 23495986

6

C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy.

Stuppia L, Gatta V, Gaspari AR, Antonucci I, Morizio E, Calabrese G, Palka G. Stuppia L, et al. Among authors: palka g. Eur J Hum Genet. 2002 Jun;10(6):388-90. doi: 10.1038/sj.ejhg.5200819. Eur J Hum Genet. 2002. PMID: 12080391

7

Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene.

Stuppia L, Gatta V, Scarciolla O, Antonucci I, Morizio E, Calabrese G, Palka G. Stuppia L, et al. Among authors: palka g. Genomics. 2005 Feb;85(2):280-3. doi: 10.1016/j.ygeno.2004.10.015. Genomics. 2005. PMID: 15676287

8

Identification of the second CFTR mutation in patients with congenital bilateral absence of vas deferens undergoing ART protocols.

Giuliani R, Antonucci I, Torrente I, Grammatico P, Palka G, Stuppia L. Giuliani R, et al. Among authors: palka g. Asian J Androl. 2010 Nov;12(6):819-26. doi: 10.1038/aja.2010.58. Epub 2010 Jul 26. Asian J Androl. 2010. PMID: 20657600 Free PMC article.

9

MS-MLPA analysis for FMR1 gene: evaluation in a routine diagnostic setting.

Gatta V, Gennaro E, Franchi S, Cecconi M, Antonucci I, Tommasi M, Palka G, Coviello D, Stuppia L, Grasso M. Gatta V, et al. Among authors: palka g. BMC Med Genet. 2013 Aug 5;14:79. doi: 10.1186/1471-2350-14-79. BMC Med Genet. 2013. PMID: 23914933 Free PMC article.

10

Different approaches in the molecular analysis of the SHOX gene dysfunctions.

Stuppia L, Gatta V, Antonucci I, Giuliani R, Palka G. Stuppia L, et al. Among authors: palka g. J Endocrinol Invest. 2010 Jun;33(6 Suppl):30-3. J Endocrinol Invest. 2010. PMID: 21057183

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

182 results

Search Page

Filters