P. Torring

发表

M. Larsen, Ieva Miceikaitė, G. Bak, 2021, Clinical case reports.

C. Shovlin, E. Buscarini, U. Sure, 2019, Orphanet Journal of Rare Diseases.

A. Green, A. Kjeldsen, P. Torring, 2018, Orphanet Journal of Rare Diseases.

A. Green, S. Möller, A. Kjeldsen, 2016, Orphanet Journal of Rare Diseases.

H. Nissen, A. Kjeldsen, P. Andersen, 2014, Acta neurologica Scandinavica.

A. Bayat, J. Vissing, M. Duno, 2022, American journal of medical genetics. Part A.

J. Rosenfeld, C. Shaw, Soo-Mi Park, 2022, American journal of medical genetics. Part A.

L. Ousager, K. Brusgaard, A. Kjeldsen, 2017, Molecular genetics & genomic medicine.

K. Brusgaard, L. Christensen, J. Karstensen, 2022, Journal of Medical Genetics.

M. Andersen, A. Gerdes, K. Brusgaard, 2016, Clinical genetics.

N. de Wind, L. Rasmussen, I. Bernstein, 2012, Human mutation.

L. Tranebjærg, Ø. Nilssen, P. Torring, 2021, European journal of medical genetics.

K. Brusgaard, A. Kjeldsen, P. Andersen, 2017, Clinical case reports.

J. Rosenfeld, B. V. van Bon, A. V. Vulto-van Silfhout, 2017, American journal of human genetics.

S. Julia, D. Wieczorek, H. Van Esch, 2022, International journal of molecular sciences.

M. Larsen, C. Fagerberg, L. Krogh, 2019, European journal of medical genetics.

P. Stankiewicz, K. Bowling, Yaping Yang, 2021, American journal of medical genetics. Part A.

L. Ousager, K. Brusgaard, A. Kjeldsen, 2014, Clinical genetics.

R. Hennekam, S. Sisodiya, A. Dionne‐Laporte, 2020, Genetics in medicine : official journal of the American College of Medical Genetics.

Q. Waisfisz, S. Julia, D. Wieczorek, 2023, European Journal of Human Genetics.

L. Ousager, K. Brusgaard, C. Brasch-Andersen, 2012, Genetic Testing and Molecular Biomarkers.

R. Hennekam, S. Sisodiya, A. Dionne‐Laporte, 2020, Genetics in Medicine.

L. Sunde, C. Lautrup, L. Christensen, 2022, Endoscopy International Open.

M. Larsen, C. Fagerberg, L. Krogh, 2019, European journal of medical genetics.

B. Lange, A. Kjeldsen, P. Torring, 2023, European Journal of Neurology.