Gentilin B - Search Results

1

Prenatal manifestation and management of a mother and child affected by spondyloperipheral dysplasia with a C-propeptide mutation in COL2A1: case report.

Bedeschi MF, Bianchi V, Gentilin B, Colombo L, Natacci F, Giglio S, Andreucci E, Trespidi L, Acaia B, Furga AS, Lalatta F. Bedeschi MF, et al. Among authors: gentilin b. Orphanet J Rare Dis. 2011 Feb 28;6:7. doi: 10.1186/1750-1172-6-7. Orphanet J Rare Dis. 2011. PMID: 21356074 Free PMC article.

2

Discordant prenatal phenotype and karyotype of monozygotic twins characterized by the unequal distribution of two cell lines investigated by different methods: a review.

Gentilin B, Guerneri S, Bianchi V, Natacci F, Colombo A, Fogliani R, Fortuna R, Coviello DA, Curcio C, Lalatta F. Gentilin B, et al. Twin Res Hum Genet. 2008 Jun;11(3):352-6. doi: 10.1375/twin.11.3.352. Twin Res Hum Genet. 2008. PMID: 18498214 Review.

3

Phenotype of five cases of prenatally diagnosed campomelic dysplasia harboring novel mutations of the SOX9 gene.

Gentilin B, Forzano F, Bedeschi MF, Rizzuti T, Faravelli F, Izzi C, Lituania M, Rodriguez-Perez C, Bondioni MP, Savoldi G, Grosso E, Botta G, Viora E, Baffico AM, Lalatta F. Gentilin B, et al. Ultrasound Obstet Gynecol. 2010 Sep;36(3):315-23. doi: 10.1002/uog.7761. Ultrasound Obstet Gynecol. 2010. PMID: 20812307 Free article.

4

Recurrence of a severe multiple congenital anomaly syndrome characterized by micrognathia, microtia, cleft palate, and short neck in two siblings.

Natacci F, Bianchi V, Guerneri S, Rizzuti T, Boito S, Gentilin B, Bedeschi MF, Lalatta F. Natacci F, et al. Among authors: gentilin b. Clin Dysmorphol. 2009 Jan;18(1):45-48. doi: 10.1097/MCD.0b013e328317c867. Clin Dysmorphol. 2009. PMID: 19050404 No abstract available.

5

Prenatal/neonatal pathology in two cases of Cornelia de Lange syndrome harboring novel mutations of NIPBL.

Lalatta F, Russo S, Gentilin B, Spaccini L, Boschetto C, Cavalleri F, Masciadri M, Gervasini C, Bentivegna A, Castronovo P, Larizza L. Lalatta F, et al. Among authors: gentilin b. Genet Med. 2007 Mar;9(3):188-94. doi: 10.1097/gim.0b013e31803183dd. Genet Med. 2007. PMID: 17413424

6

Prenatal phenotype of Nager syndrome and Rodriguez syndrome: variable expression of the same entity?

Gana S, Gentilin B, Bianchi V, Gorla S, Ceriani F, Melloni G, Lalatta F. Gana S, et al. Among authors: gentilin b. Clin Dysmorphol. 2013 Oct;22(4):135-139. doi: 10.1097/MCD.0b013e32836351c8. Clin Dysmorphol. 2013. PMID: 23811969 No abstract available.

7

Occurrence of complete arhinia in two siblings with a clinical picture of Treacher Collins syndrome negative for TCOF1, POLR1D and POLR1C mutations.

Cesaretti C, Gentilin B, Bianchi V, Melloni G, Bonaguro M, Rossi C, Meazzini C, Brusati R, Lalatta F. Cesaretti C, et al. Among authors: gentilin b. Clin Dysmorphol. 2011 Oct;20(4):229-231. doi: 10.1097/MCD.0b013e3283491725. Clin Dysmorphol. 2011. PMID: 21772136 No abstract available.

8

Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosis.

Lalatta F, Quagliarini D, Folliero E, Cavallari U, Gentilin B, Castorina P, Forzano F, Forzano S, Grosso E, Viassolo V, Naretto VG, Gattone S, Ceriani F, Faravelli F, Gargantini L. Lalatta F, et al. Among authors: gentilin b. Eur J Pediatr. 2010 Oct;169(10):1255-61. doi: 10.1007/s00431-010-1221-8. Epub 2010 May 15. Eur J Pediatr. 2010. PMID: 20473517

9

Expanding the phenotype of 22q13.3 deletion: report of a case detected prenatally.

Maitz S, Gentilin B, Colli AM, Rizzuti T, Brandolisio E, Vetro A, Zuffardi O, Guerneri S, Lalatta F. Maitz S, et al. Among authors: gentilin b. Prenat Diagn. 2008 Oct;28(10):978-80. doi: 10.1002/pd.2110. Prenat Diagn. 2008. PMID: 18821718 No abstract available.

10

Early manifestations in a cohort of children prenatally diagnosed with 47,XYY. Role of multidisciplinary counseling for parental guidance and prevention of aggressive behavior.

Lalatta F, Folliero E, Cavallari U, Di Segni M, Gentilin B, Fogliani R, Quagliarini D, Vizziello P, Monti F, Gargantini L. Lalatta F, et al. Among authors: gentilin b. Ital J Pediatr. 2012 Oct 3;38:52. doi: 10.1186/1824-7288-38-52. Ital J Pediatr. 2012. PMID: 23034220 Free PMC article.

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

25 results

Search Page

Filters