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20192019
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Fingerprint Dive into the research topics where Martina Rinelli is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

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Glypicans Medicine & Life Sciences
Mouth Abnormalities Medicine & Life Sciences
Craniofacial Abnormalities Medicine & Life Sciences
Developmental Bone Disease Medicine & Life Sciences
Hypertelorism Medicine & Life Sciences
Exome Medicine & Life Sciences
Nasodigitoacoustic syndrome Medicine & Life Sciences
X Chromosome Inactivation Medicine & Life Sciences

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Research Output 2019 2019

Novel clinical features associated with Clouston syndrome

Cammarata-Scalisi, F., Rinelli, M., Pisaneschi, E., Diociaiuti, A., Willoughby, C. E., Avendaño, A., Digilio, M. C., Novelli, A. & Callea, M., Jun 5 2019, In : International Journal of Dermatology.

Research output: Contribution to journalArticle

Pathogenic Variants in GPC4 Cause Keipert Syndrome

Amor, D. J., Stephenson, S. E. M., Mustapha, M., Mensah, M. A., Ockeloen, C. W., Lee, W. S., Tankard, R. M., Phelan, D. G., Shinawi, M., de Brouwer, A. P. M., Pfundt, R., Dowling, C., Toler, T. L., Sutton, V. R., Agolini, E., Rinelli, M., Capolino, R., Martinelli, D., Zampino, G., Dumić, M. & 10 others, Reardon, W., Shaw-Smith, C., Leventer, R. J., Delatycki, M. B., Kleefstra, T., Mundlos, S., Mortier, G., Bahlo, M., Allen, N. J. & Lockhart, P. J., Apr 5 2019, In : American Journal of Human Genetics.

Research output: Contribution to journalArticle

Glypicans
Mouth Abnormalities
Craniofacial Abnormalities
Developmental Bone Disease
Hypertelorism