Currarino Syndrome in Two Moroccan Siblings with Inherited 7q36 Deletion due to Maternal t(7;21)(q36;p11)mat: A Case Report.

El Amrani Z, Natiq A, Sbiti A, Ratbi I, Liehr T, Sefiani A, Sahli M.

DOI: 10.1159/000534432
Published: 2023-11-03
Container: Mol Syndromol
Publisher: Not recorded
Open access: no

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Cite this work

BibTeX

@article{allodium:10.1159/000534432,
  title = {Currarino Syndrome in Two Moroccan Siblings with Inherited 7q36 Deletion due to Maternal t(7;21)(q36;p11)mat: A Case Report.},
  author = {El Amrani Z and  Natiq A and  Sbiti A and  Ratbi I and  Liehr T and  Sefiani A and  Sahli M.},
  year = {2024},
  journal = {Mol Syndromol},
  doi = {10.1159/000534432},
  url = {https://doi.org/10.1159/000534432}
}

RIS

TY  - JOUR
TI  - Currarino Syndrome in Two Moroccan Siblings with Inherited 7q36 Deletion due to Maternal t(7;21)(q36;p11)mat: A Case Report.
AU  - El Amrani Z
AU  -  Natiq A
AU  -  Sbiti A
AU  -  Ratbi I
AU  -  Liehr T
AU  -  Sefiani A
AU  -  Sahli M.
PY  - 2024
JO  - Mol Syndromol
DO  - 10.1159/000534432
UR  - https://doi.org/10.1159/000534432
ER  -

APA

Z, E. A., A, N., A, S., I, R., T, L., A, S., & M., S. (2024). Currarino Syndrome in Two Moroccan Siblings with Inherited 7q36 Deletion due to Maternal t(7;21)(q36;p11)mat: A Case Report.. Mol Syndromol. https://doi.org/10.1159/000534432

Source records

europe-pmc · retrieved 2026-09-26T17:41:01.669Z