FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México-Reference-Cited by-同舟云学术

FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México

Published:2019-05 Issue:6 Volume:7 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

García‐de Teresa Benilde¹^ORCID,Frias Sara¹²^ORCID,Molina Bertha¹^ORCID,Villarreal María Teresa³^ORCID,Rodriguez Alfredo¹^ORCID,Carnevale Alessandra⁴^ORCID,López‐Hernández Gerardo⁵^ORCID,Vollbrechtshausen Lilia⁶,Olaya‐Vargas Alberto⁵^ORCID,Torres Leda¹^ORCID

Affiliation:

1. Laboratorio de Citogenética Instituto Nacional de Pediatría Ciudad de México México

2. Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México Ciudad de México México

3. Laboratorio de Enfermedades Cardiovasculares Instituto Nacional de Medicina Genómica Ciudad de México México

4. Laboratorio de Enfermedades Mendelianas Instituto Nacional de Medicina Genómica Ciudad de México México

5. Servicio de Trasplante de Células Progenitoras Hematopoyéticas Instituto Nacional de Pediatría Ciudad de México México

6. Servicio de Oncología Hospital Infantil de Tamaulipas Ciudad Victoria, Tamaulipas México

Funder

Consejo Nacional de Ciencia y Tecnología

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.710

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5. International Fanconi Anemia Registry: relation of clinical symptoms to diepoxybutane sensitivity

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