Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome.
- DOI
- 10.1186/s12887-018-1259-8
- Published
- 2018 Aug 29
- Container
- BMC pediatrics
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1186/s12887-018-1259-8,
title = {Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome.},
author = {Ghedira N and Lagarde A and Ben Ameur K and Elouej S and Sakka R and Kerkeni E and Chioukh FZ and Olschwang S and Desvignes JP and Abdelhak S and Delague V and Lévy N and Monastiri K and De Sandre-Giovannoli A},
year = {2018},
journal = {BMC pediatrics},
doi = {10.1186/s12887-018-1259-8},
url = {https://doi.org/10.1186/s12887-018-1259-8}
}RIS
TY - JOUR TI - Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome. AU - Ghedira N AU - Lagarde A AU - Ben Ameur K AU - Elouej S AU - Sakka R AU - Kerkeni E AU - Chioukh FZ AU - Olschwang S AU - Desvignes JP AU - Abdelhak S AU - Delague V AU - Lévy N AU - Monastiri K AU - De Sandre-Giovannoli A PY - 2018 JO - BMC pediatrics DO - 10.1186/s12887-018-1259-8 UR - https://doi.org/10.1186/s12887-018-1259-8 ER -
APA
N, G., A, L., K, B. A., S, E., R, S., E, K., FZ, C., S, O., JP, D., S, A., V, D., N, L., K, M., & A, D. S. (2018). Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome.. BMC pediatrics. https://doi.org/10.1186/s12887-018-1259-8
Source records
- pubmed · retrieved 2026-11-10T16:46:05.301Z