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The Review of Scientific Instruments|February 2, 2010
Quick extended x-ray absorption fine structure instrument with millisecond time scale, optimized for in situ applicationsS Khalid, W Caliebe, P Siddons, et al.
Clinical Endocrinology|June 9, 2007
GH responsiveness in a large multinational cohort of SGA children with short stature (NESTEGG) is related to the exon 3 GHR polymorphismM Tauber, W Ester, F Auriol, et al.
Clinical Epigenetics|June 13, 2019
DNA methylation profiling allows for characterization of atrial and ventricular cardiac tissues and hiPSC-CMsKirstin Hoff, Marta Lemme, Anne-Karin Kahlert, et al.
Hormone Research in Paediatrics|June 22, 2011
The use of bone age in clinical practice - part 1David D Martin, Jan M Wit, Ze'ev Hochberg, et al.
American Journal of Medical Genetics. Part A|April 29, 2010
Genotype-phenotype correlation in eight new patients with a deletion encompassing 2q31.1Diana Mitter, Barbara Delle Chiaie, Hermann-Josef Lüdecke, et al.
Molecular Genetics & Genomic Medicine|October 6, 2015
Mutations in CDK5RAP2 cause Seckel syndromeGökhan Yigit, Karen E Brown, Hülya Kayserili, et al.
Scientific Reports|July 15, 2024
LINE1-mediated epigenetic repression of androgen receptor transcription causes androgen insensitivity syndromeJelena Pozojevic, Radhika Sivaprasad, Joshua Laß, et al.
Forensic Science International. Genetics|July 5, 2020
DNA commission of the International Society of Forensic Genetics (ISFG): Recommendations on the interpretation of Y-STR results in forensic analysisLutz Roewer, Mikkel Meyer Andersen, Jack Ballantyne, et al.
Hormone Research in Paediatrics|November 28, 2013
Association analysis of ten candidate genes in a large multinational cohort of small for gestational age children and children with idiopathic short stature (NESTEGG study)L C G de Graaff, A J L Clark, M Tauber, et al.
European Journal of Medical Genetics|December 6, 2019
A post glycosylphosphatidylinositol (GPI) attachment to proteins, type 2 (PGAP2) variant identified in Mabry syndrome index cases: Molecular genetics of the prototypical inherited GPI disorderMiles D Thompson, Alexej A Knaus, Bruce A Barshop, et al.
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