[Sotos syndrome in discordant, dizygotic twins]

[Cervical cancer and DNA microarrays: tumour marker identification].

Ginecologia y obstetricia de Mexico·2007

Trisomy 3q25.1-qter and monosomy 8p23.1-pter in a patient: cytogenetic and molecular analysis with delineation of the phenotype.

American journal of medical genetics. Part A·2005

[Costello syndrome associated to a neuroblastoma. Presentation of a case].

Gaceta medica de Mexico·2000

[Assessment of a preconception preventive program in a community].

Ginecologia y obstetricia de Mexico·2000

Mexican version of the Autism Behavior Checklist: validity and reliability.

Boletin medico del Hospital Infantil de Mexico·2026

Clinical aptitude: two educational strategies for its development in cardiology residents. Quasi-experimental design.

Boletin medico del Hospital Infantil de Mexico·2026

Initial impact assessment of the current PAIDOS clinical care model for school-age children living with obesity in Mexico.

Boletin medico del Hospital Infantil de Mexico·2026

Effectiveness of the "Golden Hour" program in preventing sepsis in pediatric patients with acute lymphoblastic leukemia.

Boletin medico del Hospital Infantil de Mexico·2026

Experience of a third-level hospital teaching the laparoscopic percutaneous extraperitoneal closure technique to residents for pediatric inguinal hernia repair.

Boletin medico del Hospital Infantil de Mexico·2026

Position statement of the Mexican Academy of Pediatrics regarding strategies to prevent respiratory syncytial virus infection in Mexico's pediatric population.

Boletin medico del Hospital Infantil de Mexico·2026

Association of solute carrier family 19 member 1 (SLC19A1) A80G polymorphism with the maternal risk for having a child with Down syndrome: A systematic review and meta-analysis.

Mutation research. Reviews in mutation research·2026

Lethal Transaldolase Deficiency Mimicking Gestational Alloimmune Liver Disease: Prenatal Sonography and Identification of a Novel TALDO1 Variant.

AJP reports·2026

First report of the complete mitochondrial genome of Microtendipes famiefeus Sasa, 1996 (Diptera: Chironomidae).

Mitochondrial DNA. Part B, Resources·2026

Genetic origin and forensic analysis of han populations from four districts in Shanghai, China, based on Y-chromosome STR and SNP markers.

International journal of legal medicine·2026

A novel Doppler ultrasound approach for phenotypic assessment and follow-up of Klippel-Trénaunay syndrome: A retrospective multicenter study.

Phlebology·2026

A familial 22.59 Mb deletion of the 10q11.21q21.3 region on the neocentromeric chromosome 10 with coexistence of SMC(10): Case report and review of literature.

Cytogenetic and genome research·2026

Related Experiment Videos

[Sotos syndrome in discordant, dizygotic twins]

Related Concept Videos

[Cervical cancer and DNA microarrays: tumour marker identification].

Trisomy 3q25.1-qter and monosomy 8p23.1-pter in a patient: cytogenetic and molecular analysis with delineation of the phenotype.

[Costello syndrome associated to a neuroblastoma. Presentation of a case].

[Assessment of a preconception preventive program in a community].

Mexican version of the Autism Behavior Checklist: validity and reliability.

Clinical aptitude: two educational strategies for its development in cardiology residents. Quasi-experimental design.

Initial impact assessment of the current PAIDOS clinical care model for school-age children living with obesity in Mexico.

Effectiveness of the "Golden Hour" program in preventing sepsis in pediatric patients with acute lymphoblastic leukemia.

Experience of a third-level hospital teaching the laparoscopic percutaneous extraperitoneal closure technique to residents for pediatric inguinal hernia repair.

Position statement of the Mexican Academy of Pediatrics regarding strategies to prevent respiratory syncytial virus infection in Mexico's pediatric population.

Association of solute carrier family 19 member 1 (SLC19A1) A80G polymorphism with the maternal risk for having a child with Down syndrome: A systematic review and meta-analysis.

Lethal Transaldolase Deficiency Mimicking Gestational Alloimmune Liver Disease: Prenatal Sonography and Identification of a Novel TALDO1 Variant.

First report of the complete mitochondrial genome of Microtendipes famiefeus Sasa, 1996 (Diptera: Chironomidae).

Genetic origin and forensic analysis of han populations from four districts in Shanghai, China, based on Y-chromosome STR and SNP markers.

A novel Doppler ultrasound approach for phenotypic assessment and follow-up of Klippel-Trénaunay syndrome: A retrospective multicenter study.

A familial 22.59 Mb deletion of the 10q11.21q21.3 region on the neocentromeric chromosome 10 with coexistence of SMC(10): Case report and review of literature.

Related Experiment Videos

[Sotos syndrome in discordant, dizygotic twins]

Related Concept Videos

Related Articles