HuGE Literature Finder
|
||
Records 1-7
|
Validating genetic markers of response to recombinant human growth hormone in children with growth hormone deficiency and Turner syndrome: the PREDICT validation study.
European journal of endocrinology 2016 Dec 175 (6): 633-643. Stevens Adam, Murray Philip, Wojcik Jerome, Raelson John, Koledova Ekaterina, Chatelain Pierre, Clayton Peter, |
|
Phenotype, cancer risk, and surveillance in Beckwith-Wiedemann syndrome depending on molecular genetic subgroups.
American journal of medical genetics. Part A 2016 Jul . Maas Saskia M, Vansenne Fleur, Kadouch Daniel J M, Ibrahim Abdulla, Bliek Jet, Hopman Saskia, Mannens Marcel M, Merks Johannes H M, Maher Eamonn R, Hennekam Raoul |
|
A high incidence of WT1 abnormality in bilateral Wilms tumours in Japan, and the penetrance rates in children with WT1 germline mutation.
British journal of cancer 2015 Mar 112 (6): 1121-33. Kaneko Y, Okita H, Haruta M, Arai Y, Oue T, Tanaka Y, Horie H, Hinotsu S, Koshinaga T, Yoneda A, Ohtsuka Y, Taguchi T, Fukuzawa |
|
Different incidences of epigenetic but not genetic abnormalities between Wilms tumors in Japanese and Caucasian children.
Cancer science 2012 Jun 103 (6): 1129-35. Haruta Masayuki, Arai Yasuhito, Watanabe Naoki, Fujiwara Yuiko, Honda Shohei, Ohshima Junjiro, Kasai Fumio, Nakadate Hisaya, Horie Hiroshi, Okita Hajime, Hata Jun-Ichi, Fukuzawa Masahiro, Kaneko Yasuhi |
|
Monogenic and polygenic models detected in steroid 21-hydroxylase deficiency-related paediatric hyperandrogenism.
Hormone research 2009 Jan 71 (1): 28-37. Ezquieta B, Oyarzabal M, Barrio R, Luzuriaga C, Hermoso F, Lechuga J L, Quinteiro S, Rodríguez A, Labarta J I, Gutierrez Macias A, Gallego M, Bellón J |
|
Association between the insulin-like growth factor 2 gene (IGF2) and scores on the Eating Attitudes Test in nonclinical subjects: a family-based study.
The American journal of psychiatry 2005 Dec 162 (12): 2256-62. Bachner-Melman Rachel, Zohar Ada H, Nemanov Lubov, Heresco-Levy Uriel, Gritsenko Inga, Ebstein Richard |
|
An association between variants in the IGF2 gene and Beckwith-Wiedemann syndrome: interaction between genotype and epigenotype.
Human molecular genetics 2004 Jan 13 (2): 247-55. Murrell Adele, Heeson Sarah, Cooper Wendy N, Douglas Eleanor, Apostolidou Sophia, Moore Gudrun E, Maher Eamonn R, Reik Wo |
- Page last reviewed:Jul 30, 2019
- Page last updated:Dec 5, 2019
- Content source: