P. Müller

Detection of JAK2 exon 12 mutations in 15 patients with JAK2V617F negative polycythemia vera

T. Haferlach, H. Slawik, S. Schnittger, 2009, Haematologica.

A novel FoxD3 Variant Is Associated With Vitiligo and Elevated Thyroid Auto-Antibodies.

K. Badenhoop, M. Stumvoll, P. Kovacs, 2015, The Journal of clinical endocrinology and metabolism.

[A rare inborn error of intracellular processing of cobalamine presenting with microcephalus and megaloblastic anemia: a report of 3 children].

J. Hennermann, G. Horneff, P. Müller, 2007, Klinische Padiatrie.

Validation of the Phenylalanine/Tyrosine Ratio Determined by Tandem Mass Spectrometry: Sensitive Newborn Screening for Phenylketonuria

U. Ceglarek, J. Thiery, W. Kiess, 2002, Clinical chemistry and laboratory medicine.