about
Say-Meyer syndrome: additional manifestations in a new patient and phenotypic assessment.Fetus with Casamassima-Morton-Nance Syndrome and Limb-Body Wall Defect: Presentation of a Novel Association and Review of the Phenotype.Congenital hemangioma in spondylocostal dysostosis: a novel associationBranchiootorenal 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.Severe Intrauterine Amputations in One Dichorionic Twin With Pentalogy of Cantrell: Further Evidence and Consideration for Mechanical Teratogenesis.Bilateral tibial hemimelia type 1 (1a and 1b) with T9 and T10 hemivertebrae: a novel association.Prevalence, Mortality, and Spatial Distribution of Gastroschisis in Mexico.Familial occurrence of gastroschisis: a population-based overview on recurrence risk, sex-dependent influence, and geographical distribution.SPINAL MUSCULAR ATROPHY TYPE 1 AND POLAND SYNDROME: A NOVEL ASSOCIATION IN A MEXICAN FEMALE INFANT.Thanatophoric dysplasia type 1 with cloverleaf skull in a dichorionic twin.Genetic variants conferring susceptibility to gastroschisis: a phenomenon restricted to the interaction with the environment?Syringomyelia in VACTERL-H association: a new neurological feature in an adult patient.[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?]Male-to-male transmission of Laurin-Sandrow syndrome in a Mexican familyWhole exome sequencing identifies multiple novel candidate genes in familial gastroschisisA clinical-pathogenetic approach on associated anomalies and chromosomal defects supports novel candidate critical regions and genes for gastroschisisBioinformatic Analysis of Gene Variants from Gastroschisis Recurrence Identifies Multiple Novel Pathogenetic Pathways: Implication for the Closure of the Ventral Body WallFryns syndrome with vertebral defects: a novel association in a Mexican infant
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P50
description
hulumtues
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onderzoeker
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researcher
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հետազոտող
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name
Victor Michael Salinas-Torres
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Victor Michael Salinas-Torres
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Victor Michael Salinas-Torres
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Victor Michael Salinas-Torres
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Victor Michael Salinas-Torres
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Victor Michael Salinas-Torres
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Victor Michael Salinas-Torres
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Victor Michael Salinas-Torres
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Victor Michael Salinas-Torres
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Victor Michael Salinas-Torres
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Michael
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Victor Michael Salinas-Torres
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Victor Michael Salinas-Torres
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Victor Michael Salinas-Torres
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Victor Michael Salinas-Torres
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Victor Michael Salinas-Torres
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P106
P21
P31
P496
0000-0003-4852-8026