Lista de obras - Victor Michael Salinas-Torres

A clinical-pathogenetic approach on associated anomalies and chromosomal defects supports novel candidate critical regions and genes for gastroschisis

artículo científico publicado en 2018

Bilateral tibial hemimelia type 1 (1a and 1b) with T9 and T10 hemivertebrae: a novel association

artículo científico publicado en 2013

Bioinformatic Analysis of Gene Variants from Gastroschisis Recurrence Identifies Multiple Novel Pathogenetic Pathways: Implication for the Closure of the Ventral Body Wall ⬇️

scientific article published on 09 May 2019

Branchiootorenal syndrome with skeletal defects: a novel association in a Mexican child

artículo científico publicado en 2015

Callosotomy in a girl with refractory epilepsy and Smith-Magenis syndrome

artículo científico publicado en 2013

Clinical, cytogenetic, environmental and inheritance findings in Mexican neonates with VACTERL association

artículo científico publicado en 2014

Congenital hemangioma in spondylocostal dysostosis: a novel association

artículo científico publicado en 2016

Familial occurrence of gastroschisis: a population-based overview on recurrence risk, sex-dependent influence, and geographical distribution

artículo científico publicado en 2018

Fetus with Casamassima-Morton-Nance Syndrome and Limb-Body Wall Defect: Presentation of a Novel Association and Review of the Phenotype.

artículo científico

Fryns syndrome with vertebral defects: a novel association in a Mexican infant

Genetic variants conferring susceptibility to gastroschisis: a phenomenon restricted to the interaction with the environment?

artículo científico publicado en 2018

Male-to-male transmission of Laurin-Sandrow syndrome in a Mexican family

artículo científico publicado en 2014

Prevalence, Mortality, and Spatial Distribution of Gastroschisis in Mexico

artículo científico publicado en 2018

SPINAL MUSCULAR ATROPHY TYPE 1 AND POLAND SYNDROME: A NOVEL ASSOCIATION IN A MEXICAN FEMALE INFANT.

artículo científico publicado en 2015

Say-Meyer syndrome: additional manifestations in a new patient and phenotypic assessment

artículo científico publicado en 2015

Severe Intrauterine Amputations in One Dichorionic Twin With Pentalogy of Cantrell: Further Evidence and Consideration for Mechanical Teratogenesis.

artículo científico publicado en 2017

Syringomyelia in VACTERL-H association: a new neurological feature in an adult patient.

artículo científico publicado en 2015

Thanatophoric dysplasia type 1 with cloverleaf skull in a dichorionic twin.

artículo científico publicado en 2015

Whole exome sequencing identifies multiple novel candidate genes in familial gastroschisis

artículo científico publicado en 2020

[Unusual branchial arch, dermoepidermal and nervous system anomalies in a neonate with VACTERL-H syndrome]

artículo científico publicado en 2012

[VACTERL-H association with tibial agenesis. Expansion of the clinical phenotype?]

scientific article published on 20 December 2012

Lista de obras de Victor Michael Salinas-Torres

A clinical-pathogenetic approach on associated anomalies and chromosomal defects supports novel candidate critical regions and genes for gastroschisis

Bilateral tibial hemimelia type 1 (1a and 1b) with T9 and T10 hemivertebrae: a novel association

Bioinformatic Analysis of Gene Variants from Gastroschisis Recurrence Identifies Multiple Novel Pathogenetic Pathways: Implication for the Closure of the Ventral Body Wall ⬇️

Branchiootorenal syndrome with skeletal defects: a novel association in a Mexican child

Callosotomy in a girl with refractory epilepsy and Smith-Magenis syndrome

Clinical, cytogenetic, environmental and inheritance findings in Mexican neonates with VACTERL association

Congenital hemangioma in spondylocostal dysostosis: a novel association

Familial occurrence of gastroschisis: a population-based overview on recurrence risk, sex-dependent influence, and geographical distribution

Fetus with Casamassima-Morton-Nance Syndrome and Limb-Body Wall Defect: Presentation of a Novel Association and Review of the Phenotype.

Fryns syndrome with vertebral defects: a novel association in a Mexican infant

Genetic variants conferring susceptibility to gastroschisis: a phenomenon restricted to the interaction with the environment?

Male-to-male transmission of Laurin-Sandrow syndrome in a Mexican family

Prevalence, Mortality, and Spatial Distribution of Gastroschisis in Mexico

SPINAL MUSCULAR ATROPHY TYPE 1 AND POLAND SYNDROME: A NOVEL ASSOCIATION IN A MEXICAN FEMALE INFANT.

Say-Meyer syndrome: additional manifestations in a new patient and phenotypic assessment

Severe Intrauterine Amputations in One Dichorionic Twin With Pentalogy of Cantrell: Further Evidence and Consideration for Mechanical Teratogenesis.

Syringomyelia in VACTERL-H association: a new neurological feature in an adult patient.

Thanatophoric dysplasia type 1 with cloverleaf skull in a dichorionic twin.

Whole exome sequencing identifies multiple novel candidate genes in familial gastroschisis

[Unusual branchial arch, dermoepidermal and nervous system anomalies in a neonate with VACTERL-H syndrome]

[VACTERL-H association with tibial agenesis. Expansion of the clinical phenotype?]