Bibliografia UJ CM

1/2
Ella M.M.A. Martin, Annabelle Enriquez, Duncan B. Sparrow, David T. Humphreys, Aideen M. McInerney-Leo, Paul J. Leo, Emma L. Duncan, Kavitha R. Iyer, Joelene A. Greasby, Eddie Ip, Eleni Giannoulatou, Delicia Sheng, Elizabeth Wohler, Clémantine Dimartino, Jeanne Amiel, Yline Capri, Daphné Lehalle, Adi Mory, Yael Wilnai, Yael Lebenthal, Ali G. Gharavi, Grażyna G. Krzemień, Monika Miklaszewska, Robert D. Steiner, Cathy Raggio, Robert Blank, Hagit Baris Feldman, Hila Milo Rasouly, Nara L.M. Sobreira, Rebekah Jobling, Christopher T. Gordon, Philip F. Giampietro, Sally L. Dunwoodie, Gavin Chapman.
Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice.
Human Molecular Genetics
2020 : Vol. 29, nr 22, s. 3662-3678, il., bibliog. 72 poz., abstr.
Autor korespondencyjny: Gavin Chapman.
p-ISSN: 0964-6906
AZ
ORG
AIF
IF: 6.150
Adres url:
Streszczenie w PubMed:
DOI:
2/2
Moshe Phillp, Yael Lebenthal, Jan Lebl, Nehama Zuckerman-Levin, Maria Korpal-Szczyrska, Jorge Sales Marques, Adam Steensberg, Kirsten Jons, Anne-Marie Kappelgaard, Lourdes Ibanez, The European Norditropin SGA Study Group.
European multicentre study in children born small for gestational age with persistent short stature : comparison of continuous and discontinuous growth hormone treatment regimens.
Horm. Res.
2009 : Vol. 71, nr 1, s. 52-59, il., bibliogr. 37 poz., abstr.
p-ISSN: 0301-0163
AZ
ORG
AIF
IF: 1.730
Wyświetl ponownie stosując format: