Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1991 1
1992 2
1993 4
1995 3
1996 1
1997 1
2015 1
2016 1
2017 1
2018 1
2020 1
2021 1
2022 1
Text availability
Article attribute
Article type
Publication date

Search Results

18 results
Results by year
Filters applied: . Clear all
Page 1
RAPADILINO syndrome.
Vargas FR, de Almeida JC, Llerena Júnior JC, Reis DF. Vargas FR, et al. Among authors: llerena junior jc. Am J Med Genet. 1992 Dec 1;44(6):716-9. doi: 10.1002/ajmg.1320440604. Am J Med Genet. 1992. PMID: 1481838 Review.
Fetal Skeletal Lethal Dysplasia: Case Report.
Savoldi AM, Villar MAM, Machado HN, Llerena Júnior JC. Savoldi AM, et al. Among authors: llerena junior jc. Rev Bras Ginecol Obstet. 2017 Oct;39(10):576-582. doi: 10.1055/s-0037-1603943. Epub 2017 Aug 7. Rev Bras Ginecol Obstet. 2017. PMID: 28783850 Free article. Review. English.
Xp-duplications with and without sex reversal.
Baumstark A, Barbi G, Djalali M, Geerkens C, Mitulla B, Mattfeldt T, de Almeida JC, Vargas FR, Llerena Júnior JC, Vogel W, Just W. Baumstark A, et al. Among authors: llerena junior jc. Hum Genet. 1996 Jan;97(1):79-86. doi: 10.1007/BF00218838. Hum Genet. 1996. PMID: 8557267 Review.
Cystic fibrosis and deafness.
Llerena Júnior JC, Degrave W, De Miranda A, Suffys P. Llerena Júnior JC, et al. J Med Genet. 1993 Jul;30(7):621. doi: 10.1136/jmg.30.7.621. J Med Genet. 1993. PMID: 8411044 Free PMC article. No abstract available.
A newborn screening pilot study using methylation-sensitive high resolution melting on dried blood spots to detect Prader-Willi and Angelman syndromes.
Ferreira IR, Costa RA, Gomes LHF, Dos Santos Cunha WD, Tyszler LS, Freitas S, Llerena Junior JC, de Vasconcelos ZFM, Nicholls RD, Guida LDC. Ferreira IR, et al. Among authors: llerena junior jc. Sci Rep. 2020 Aug 3;10(1):13026. doi: 10.1038/s41598-020-69750-0. Sci Rep. 2020. PMID: 32747801 Free PMC article.
Peters' plus syndrome.
de Almeida JC, Llerena Júnior JC. de Almeida JC, et al. Among authors: llerena junior jc. Am J Med Genet. 1993 Aug 1;47(1):125. doi: 10.1002/ajmg.1320470129. Am J Med Genet. 1993. PMID: 8368243 No abstract available.
Clinical Spectrum and Tumour Risk Analysis in Patients with Beckwith-Wiedemann Syndrome Due to CDKN1C Pathogenic Variants.
Cardoso LCA, Parra A, Gil CR, Arias P, Gallego N, Romanelli V, Kantaputra PN, Lima L, Llerena Júnior JC, Arberas C, Guillén-Navarro E, Nevado J, Spanish OverGrowth Registry Initiative, Tenorio-Castano J, Lapunzina P. Cardoso LCA, et al. Among authors: llerena junior jc. Cancers (Basel). 2022 Aug 5;14(15):3807. doi: 10.3390/cancers14153807. Cancers (Basel). 2022. PMID: 35954470 Free PMC article.
Another example favouring the location of BPES at 3q2.
de Almeida JC, Llerena Júnior JC, Gonçalves Neto JB, Jung M, Martins RR. de Almeida JC, et al. Among authors: llerena junior jc. J Med Genet. 1993 Jan;30(1):86. doi: 10.1136/jmg.30.1.86. J Med Genet. 1993. PMID: 8481195 Free PMC article. No abstract available.
18 results