Palka G - Search Results

1

Non-invasive prenatal screening: A 20-year experience in Italy.

Palka C, Guanciali-Franchi P, Morizio E, Alfonsi M, Papponetti M, Sabbatinelli G, Palka G, Calabrese G, Benn P. Palka C, et al. Among authors: palka g. Eur J Obstet Gynecol Reprod Biol X. 2019 May 18;3:100050. doi: 10.1016/j.eurox.2019.100050. eCollection 2019 Jul. Eur J Obstet Gynecol Reprod Biol X. 2019. PMID: 31403132 Free PMC article. Review.

2

A case of triploidy detected by crosstrimester test.

Guanciali-Franchi P, Iezzi I, Matarrelli B, Morizio E, Calabrese G, Palka G. Guanciali-Franchi P, et al. Among authors: palka g. J Prenat Med. 2012 Jul;6(3):55-6. J Prenat Med. 2012. PMID: 23181174 Free PMC article.

3

An 11.4-Mb Interstitial Deletion in a Fetus with No Apparent Phenotypic Alterations.

Guanciali-Franchi P, Celentano C, Alfonsi M, Palka C, Di Pasqua G, Matarrelli B, Palka G. Guanciali-Franchi P, et al. Among authors: palka g. Mol Syndromol. 2017 Jan;8(1):42-44. doi: 10.1159/000452967. Epub 2016 Dec 3. Mol Syndromol. 2017. PMID: 28232782 Free PMC article.

4

Prenatal diagnosis using the triple test.

Palka G, Guanciali Franchi P, Papponetti M, Marcuccitti J, Morizio E, Calabrese G, Stuppia L, Di Ilio C. Palka G, et al. Minerva Ginecol. 1998 Oct;50(10):411-5. Minerva Ginecol. 1998. PMID: 9866951

5

De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects.

Alfonsi M, Palka C, Morizio E, Gatta V, Antonucci I, Ruggeri G, Chiarelli F, Stuppia L, Palka G, Calabrese G. Alfonsi M, et al. Among authors: palka c, palka g. Clin Dysmorphol. 2013 Jul;22(3):132-134. doi: 10.1097/MCD.0b013e328363023b. Clin Dysmorphol. 2013. PMID: 23722703 No abstract available.

6

Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment.

Palka C, Alfonsi M, Mohn A, Cerbo R, Guanciali Franchi P, Fantasia D, Morizio E, Stuppia L, Calabrese G, Zori R, Chiarelli F, Palka G. Palka C, et al. Among authors: palka g. Pediatrics. 2012 Jan;129(1):e183-8. doi: 10.1542/peds.2010-2094. Epub 2011 Dec 5. Pediatrics. 2012. PMID: 22144704

7

Prenatal diagnosis of a family affected by brachydactyly type A1 with a mutation in IHH: a useful lesson.

Palka C, Antonucci I, Alfonsi M, Bedeschi MF, Mohn A, Lalatta F, Chiarelli F, Palka G, Stuppia L. Palka C, et al. Among authors: palka g. Clin Dysmorphol. 2012 Jul;21(3):137-140. doi: 10.1097/MCD.0b013e328350af23. Clin Dysmorphol. 2012. PMID: 22406540 No abstract available.

8

Case report of newborn with de novo partial trisomy 2q31.2-37.3 and monosomy 9p24.3.

Colangelo M, Alfonsi M, Palka C, Zio EZ, Renzo SD, Guanciali-Franchi P, Palka G. Colangelo M, et al. Among authors: palka g. J Genet. 2018 Mar;97(1):311-317. J Genet. 2018. PMID: 29666350 Free article.

9

Molecular characterization of two extra marker chromosomes detected at prenatal diagnosis.

Calabrese G, Stuppia L, Mingarelli R, Guanciali Franchi P, Peila R, Morizio E, Antonucci A, Palka G. Calabrese G, et al. Among authors: palka g. Ann Genet. 1994;37(3):135-8. Ann Genet. 1994. PMID: 7847794

10

The methylenetethrahydrofolate reductase (MTHFR) C677T polymorphism and male infertility in Italy.

Stuppia L, Gatta V, Scarciolla O, Colosimo A, Guanciali-Franchi P, Calabrese G, Palka G. Stuppia L, et al. Among authors: palka g. J Endocrinol Invest. 2003 Jul;26(7):620-2. doi: 10.1007/BF03347018. J Endocrinol Invest. 2003. PMID: 14594111

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