Found: 31
Select item for more details and to access through your institution.
Heterogeneous Diagnoses Underlying Radial Ray Anomalies.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Hybridization vs. Bond Stretching Isomerism in Ru(II) Cyclometalated Complexes of 2-Phenylpyridine.
- Published in:
- Molecules, 2012, v. 17, n. 1, p. 34, doi. 10.3390/molecules17010034
- By:
- Publication type:
- Article
On the π Coordination of Organometallic Fullerene Complexes.
- Published in:
- Molecules, 2011, v. 16, n. 6, p. 4652, doi. 10.3390/molecules16064652
- By:
- Publication type:
- Article
Translocación recíproca 46,XY, t(1;f)(q21;q13), en un adolescente con cementoma gigantiforme no familiar.
- Published in:
- Boletín Médico del Hospital Infantil de México, 2002, v. 59, n. 2, p. 118
- By:
- Publication type:
- Article
Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCG.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 4, p. 2334, doi. 10.3390/ijms23042334
- By:
- Publication type:
- Article
Presence of 15p Marker D15Z1 on the Short Arm of Acrocentric Chromosomes is Associated with Aneuploid Offspring in Mexican Couples.
- Published in:
- International Journal of Molecular Sciences, 2019, v. 20, n. 21, p. 5251, doi. 10.3390/ijms20215251
- By:
- Publication type:
- Article
Reversion from basal histone H4 hypoacetylation at the replication fork increases DNA damage in FANCA deficient cells.
- Published in:
- PLoS ONE, 2024, v. 19, n. 5, p. 1, doi. 10.1371/journal.pone.0298032
- By:
- Publication type:
- Article
Erratum to: Germline Mutations in NKX2-5, GATA4, and CRELD1 are Rare in a Mexican Sample of Down Syndrome Patients with Endocardial Cushion and Septal Heart Defects.
- Published in:
- 2015
- By:
- Publication type:
- Erratum
Germline Mutations in NKX2- 5, GATA4, and CRELD1 are Rare in a Mexican Sample of Down Syndrome Patients with Endocardial Cushion and Septal Heart Defects.
- Published in:
- Pediatric Cardiology, 2015, v. 36, n. 4, p. 802, doi. 10.1007/s00246-014-1091-3
- By:
- Publication type:
- Article
Investigation of Structural and Optoelectronic Properties of Organic Semiconductor Film Based on 8-Hydroxyquinoline Zinc.
- Published in:
- Electronics (2079-9292), 2021, v. 10, n. 2, p. 117, doi. 10.3390/electronics10020117
- By:
- Publication type:
- Article
Nonclonal Chromosome Aberrations and Genome Chaos in Somatic and Germ Cells from Patients and Survivors of Hodgkin Lymphoma.
- Published in:
- Genes, 2019, v. 10, n. 1, p. 37, doi. 10.3390/genes10010037
- By:
- Publication type:
- Article
Genomic chaos in peripheral blood lymphocytes of Hodgkin's lymphoma patients one year after ABVD chemotherapy/radiotherapy.
- Published in:
- Environmental & Molecular Mutagenesis, 2018, v. 59, n. 8, p. 755, doi. 10.1002/em.22216
- By:
- Publication type:
- Article
Hydroxyurea induces chromosomal damage in G2 and enhances the clastogenic effect of mitomycin C in Fanconi anemia cells.
- Published in:
- Environmental & Molecular Mutagenesis, 2015, v. 56, n. 5, p. 457, doi. 10.1002/em.21938
- By:
- Publication type:
- Article
Anemia de Fanconi, Parte 1. Diagnóstico citogenético.
- Published in:
- Acta Pediatrica de Mexico, 2022, v. 43, n. 2, p. 102, doi. 10.18233/apm43no2pp102-1282393
- By:
- Publication type:
- Article
Translocaciones crípticas de cromosomas acrocéntricos en muestras de tejido de aborto aneuploide.
- Published in:
- Acta Pediatrica de Mexico, 2015, v. 36, n. 5, p. 374, doi. 10.18233/APM36No5pp374-382
- By:
- Publication type:
- Article
Diagnóstico clínico y de laboratorio de la anemia de Fanconi.
- Published in:
- Acta Pediatrica de Mexico, 2012, v. 33, n. 1, p. 38
- By:
- Publication type:
- Article
Expresión diferencial del ARN en la anemia de Fanconi. Una probable característica fenotípica.
- Published in:
- Acta Pediatrica de Mexico, 2006, v. 27, n. 1, p. 24
- By:
- Publication type:
- Article
Capture of Fullerenes in Cages and Rings by Forming Metal-π Bond Arene Interactions.
- Published in:
- Materials (1996-1944), 2021, v. 14, n. 12, p. 3424, doi. 10.3390/ma14123424
- By:
- Publication type:
- Article
Frequent copy number variants in a cohort of Mexican-Mestizo individuals.
- Published in:
- Molecular Cytogenetics (17558166), 2023, v. 16, n. 1, p. 1, doi. 10.1186/s13039-022-00631-z
- By:
- Publication type:
- Article
Detection of short-term chromosomal damage due to therapeutic <sup>131</sup>I exposure in patients with thyroid cancer.
- Published in:
- Clinical & Translational Investigation / Revista de Investigación Clínica, 2010, v. 62, n. 1, p. 31
- By:
- Publication type:
- Article
Duplication 2p and Monosomy 8p in mosaicism: clinical, molecular cytogenetic and molecular markers of a unique case.
- Published in:
- Clinical & Translational Investigation / Revista de Investigación Clínica, 2007, v. 59, n. 6, p. 444
- By:
- Publication type:
- Article
Variabilidad clínica y citogenética en doce familias mexicanas con anemia de Fanconi y su relación con el grupo de complementación al que pertenecen.
- Published in:
- Clinical & Translational Investigation / Revista de Investigación Clínica, 1999, v. 51, n. 5, p. 273
- By:
- Publication type:
- Article
A Boolean network model of the FA/BRCA pathway.
- Published in:
- Bioinformatics, 2012, v. 28, n. 6, p. 858
- By:
- Publication type:
- Article
Non-classical 1p36 deletion in a patient with Duane retraction syndrome: case report and literature review.
- Published in:
- Molecular Cytogenetics (17558166), 2020, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13039-020-00510-5
- By:
- Publication type:
- Article
Report of a patient with a de novo non-recurrent duplication of 17p11.2p12 and Yq11 deletion.
- Published in:
- Molecular Cytogenetics (17558166), 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13039-019-0438-0
- By:
- Publication type:
- Article
Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogenetics.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
7p15 deletion as the cause of hand-foot-genital syndrome: a case report, literature review and proposal of a minimum region for this phenotype.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
Evaluation of Clastogenic/Aneugenic Damage Using the FISH Micronucleus Assay in Mice Exposed to Chromium (VI).
- Published in:
- In Vivo, 2023, v. 37, n. 4, p. 1666, doi. 10.21873/invivo.13252
- By:
- Publication type:
- Article
Interstitial deletion of 2q24.2: Further delineation of an emerging syndrome associated with intellectual disability, severe hypotonia and moderate intrauterine growth restriction.
- Published in:
- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 3, p. 824, doi. 10.1002/ajmg.a.36347
- By:
- Publication type:
- Article
FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México.
- Published in:
- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 6, p. N.PAG, doi. 10.1002/mgg3.710
- By:
- Publication type:
- Article
Exohedral complexes of large fullerenes, a theoretical approach.
- Published in:
- Journal of Molecular Modeling, 2017, v. 23, n. 5, p. 1, doi. 10.1007/s00894-017-3346-4
- By:
- Publication type:
- Article