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Search Results - Barahona, Aldo F. Ponce
Search Results - Barahona, Aldo F. Ponce
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A novel description of a syndrome consisting of 7q21.3 deletion including DYNC1I1 with preserved DLX5/6 without ectrodactyly: a case report
by
Ramos-Zaldívar, Héctor M
,
Martínez-Irías, Daniel G
,
Espinoza-Moreno, Nelson A
,
Napky-Rajo, José S
,
Bueso-Aguilar, Tulio A
,
Reyes-Perdomo, Karla G
,
Montes-Gambarelli, Jimena A
,
Euceda, Isis M
,
Ponce-Barahona, Aldo F
,
Gámez-Fernández, Carlos A
,
Moncada-Arita, Wilberg A
,
Palomo-Bermúdez, Victoria A
,
Jiménez-Faraj, Julia E
,
Hernández-Padilla, Amanda G
,
Olivera, Denys A
,
Robertson, Kevin J
,
Leiva-Sanchez, Luis A
,
Herrera-Paz, Edwin Francisco
Published in
Journal of medical case reports
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SAFETY AND EFFECTIVENESS OF A LOW MOLECULAR WEIGHT HEPARIN IN PULMONARY EMBOLISM ASSOCIATED WITH CHEMOTHERAPY-INDUCED HEART FAILURE AND SEVERE THROMBOCYTOPENIA
by
Barahona, Aldo F. Ponce
,
Jerjes-Sanchez, Carlos
,
Vazquez, Jose G. Paredes
,
Ibarra, Arturo A. Martinez
,
Garza, Silvia M. Galindo
,
Lozano, Jaime A. Guajardo
,
Garza, Hector Lopez de la
,
Harrison, Jorge A. Joya
,
Casanova, Jose A. Salinas
,
Almaguer, Erasmo De la Peña
Published in
Journal of the American College of Cardiology
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Journal Of Medical Case Reports
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Journal Of The American College Of Cardiology
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Abnormalities, Multiple - Genetics
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Abnormalities, Multiple - Physiopathology
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Abnormalities, Multiple - Psychology
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Adult
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Birth Defects
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Case Report
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Chromosome Aberrations
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Chromosome Deletion
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Chromosomes, Human, Pair 7
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Col1A2
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Cytoplasmic Dyneins - Genetics
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Deafness
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Deletion 7Q21.3
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Diagnosis
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Disease
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Dlx5/6
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Dss1
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Dync1I1
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Ectrodactyly
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Gene Mutations
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Doaj Directory Of Open Access Journals
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Ingentaconnect Journals
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Road: Directory Of Open Access Scholarly Resources
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Springer Nature - Connect Here First To Enable Access
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