Search Page
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
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2018 | 1 |
2019 | 1 |
2020 | 1 |
2021 | 3 |
2024 | 0 |
Search Results
6 results
Results by year
Filters applied: . Clear all
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
An additional patient with a homozygous mutation in DCPS contributes to the delination of Al-Raqad syndrome.
Am J Med Genet A. 2018 Dec;176(12):2781-2786. doi: 10.1002/ajmg.a.40488. Epub 2018 Oct 5.
Am J Med Genet A. 2018.
PMID: 30289615
Review.
A heterozygous, intragenic deletion of CNOT2 recapitulates the phenotype of 12q15 deletion syndrome.
Alesi V, Loddo S, Calì F, Orlando V, Genovese S, Ferretti D, Calacci C, Calvieri G, Falasca R, Ulgheri L, Drago F, Dallapiccola B, Baban A, Novelli A.
Alesi V, et al. Among authors: calvieri g.
Am J Med Genet A. 2019 Aug;179(8):1615-1621. doi: 10.1002/ajmg.a.61217. Epub 2019 May 30.
Am J Med Genet A. 2019.
PMID: 31145527
Review.
Item in Clipboard
PPP1R21-related syndromic intellectual disability: Report of an adult patient and review.
Loddo S, Alesi V, Radio FC, Genovese S, Di Tommaso S, Calvieri G, Orlando V, Bertini E, Dentici ML, Novelli A, Dallapiccola B.
Loddo S, et al. Among authors: calvieri g.
Am J Med Genet A. 2020 Dec;182(12):3014-3022. doi: 10.1002/ajmg.a.61889. Epub 2020 Sep 27.
Am J Med Genet A. 2020.
PMID: 32985083
Review.
Item in Clipboard
Clinical Application of Easychip 8x15K Platform in 4106 Pregnancies Without Ultrasound Anomalies.
Orlando V, Alesi V, Di Giacomo G, Canestrelli M, Calacci C, Nardone AM, Calvieri G, Liambo MT, Sallicandro E, Di Tommaso S, Di Gregorio MG, Corrado F, Barrano G, Niceta M, Dallapiccola B, Novelli A.
Orlando V, et al. Among authors: calvieri g.
Reprod Sci. 2021 Apr;28(4):1142-1149. doi: 10.1007/s43032-020-00419-9. Epub 2021 Jan 6.
Reprod Sci. 2021.
PMID: 33409881
Item in Clipboard
A New Intronic Variant in ECEL1 in Two Patients with Distal Arthrogryposis Type 5D.
Alesi V, Sessini F, Genovese S, Calvieri G, Sallicandro E, Ciocca L, Mingoia M, Novelli A, Moi P.
Alesi V, et al. Among authors: calvieri g.
Int J Mol Sci. 2021 Feb 20;22(4):2106. doi: 10.3390/ijms22042106.
Int J Mol Sci. 2021.
PMID: 33672664
Free PMC article.
Item in Clipboard
Homozygous HESX1 and COL1A1 Gene Variants in a Boy with Growth Hormone Deficiency and Early Onset Osteoporosis.
Alesi V, Dentici ML, Genovese S, Loddo S, Bellacchio E, Orlando V, Di Tommaso S, Catino G, Calacci C, Calvieri G, Pompili D, Ubertini G, Dallapiccola B, Capolino R, Novelli A.
Alesi V, et al. Among authors: calvieri g.
Int J Mol Sci. 2021 Jan 13;22(2):750. doi: 10.3390/ijms22020750.
Int J Mol Sci. 2021.
PMID: 33451138
Free PMC article.
Item in Clipboard
Cite
Cite