Результаты поиска - Niklas Dahl

Whole genome sequencing of familial isolated oesophagus atresia uncover shared structural variants по Joakim Klar, Helene Engstrand-Lilja, Khurram Maqbool, Jonas Mattisson, Lars Feuk, Niklas Dahl

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Homozygous GRID2 missense mutation predicts a shift in the D-serine binding domain of GluD2 in a case with generalized brain atrophy and unusual clinical features по Zafar Ali, Shumaila Zulfiqar, Joakim Klar, Johan Wikström, Farid Ullah, Ayaz Khan, Uzma Abdullah, Shahid Baig, Niklas Dahl

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Palmoplantar keratoderma and digital clubbing in 2 sisters with hypertrophic osteoarthropathy по Daniel Eriksson, MD, PhD, David Gyll, MD, Marie Virtanen, MD, Niklas Dahl, MD, PhD, Joakim Klar, PhD, Eva-Lena Stattin, MD, PhD

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