See veebileht kasutab küpsiseid kasutaja sessiooni andmete hoidmiseks. Veebilehe kasutamisega nõustute ETISe kasutustingimustega. Loe rohkem
Olen nõus

Variation in FGF1, FOXE1, and TIMP2 genes is associated with nonsyndromic cleft lip with or without cleft palate

Nikopensius, T.; Kempa, I.; Ambrozaitytė, L.; Jagomägi, T.; Saag, M.; Matulevičienė, A.; Utkus, A.; Krjutškov, K.; Tammekivi, V.; Piekuse, L.; Akota, l.; Barkane, B.; Krumina, A.; Klovins, J.; Lace, B.; Kučinskas, V.; Metspalu, A. (2011). Variation in FGF1, FOXE1, and TIMP2 genes is associated with nonsyndromic cleft lip with or without cleft palate. Birth Defects Research Part A: Clinical and Molecular Teratology, 91 (4), 218−225.
ajakirjaartikkel
Nikopensius, T.; Kempa, I.; Ambrozaitytė, L.; Jagomägi, T.; Saag, M.; Matulevičienė, A.; Utkus, A.; Krjutškov, K.; Tammekivi, V.; Piekuse, L.; Akota, l.; Barkane, B.; Krumina, A.; Klovins, J.; Lace, B.; Kučinskas, V.; Metspalu, A.
  • Inglise
Birth Defects Research Part A: Clinical and Molecular Teratology
1542-0760
91
4
Clin M
2011
218225
Ilmunud
1.1. Teadusartiklid, mis on kajastatud Web of Science andmebaasides Science Citation Index Expanded, Social Sciences Citation Index, Arts & Humanities Citation Index ja/või andmebaasis Scopus (v.a. kogumikud)
WOS

Viited terviktekstile

Lisainfo

Artikkel on aktsepteeritud avaldasmiseks. Date:23-Jan-2011 Manuscript number: BDRA-10-0215.R2 Dear Dr. Jagomägi: I am pleased to inform you that your revised manuscript,"Variation in FGF1, FOXE1, and TIMP2 genes is associated with nonsyndromic cleft lip with or without cleft palate," is acceptable for publication in Birth Defects Research Part A: Clinical and Molecular Teratology. Please note that you will receive email notification when your proofs are available to download and correct. Within about 3 weeks after your corrected proofs are returned to the publisher, your article will be posted online in "Early View," at http://www3.interscience.wiley.com/cgi-bin/jissue/104548475. Once all of the articles for a given issue have been proofed and corrected, the contents of the issue will be organized according to the print version and posted as the current issue at http://www3.interscience.wiley.com/cgi-bin/jhome/102526943. Please note that Wiley-Blackwell offers an open access publication option for a fee. More information is available through the OnlineOpen link on the journal web site (http://www3.interscience.wiley.com/journal/117928902/grouphome/home.html). Thank you for submitting your interesting manuscript to Birth Defects Research Part A: Clinical and Molecular Teratology. I look forward to seeing more of your work in the future. Sincerely, Professor Diana Juriloff, Ph.D. Editor-in-Chief Birth Defects Research Part A: Clinical and Molecular Teratology bdraed@interchange.ubc.ca