Antecedentes: alrededor de 15% de todos los embarazos termina en aborto. En
aproximadamente 60% de todas las p�rdidas se encuentran anormalidades cromos�micas como …

… Lorena Orozco,* Margarita Ch�vez,** Yolanda Salda�a,* Rafael Vel�zquez,* Alessandra
Carnevale,*** Ariadna Gonz�lez-del �ngel,**Silvia Jim�nez* … Csanady L, Seto-Young D�…

Context: Heterozygous mutations in the aggrecan gene (ACAN) cause autosomal dominant
short stature with accelerated skeletal maturation. Objective: We sought to characterize the …

Background: About 15% of all pregnancies end in abortion. In approximately 60% of all
losses are chromosomal abnormalities as a cause of pregnancy loss. Objective: To determine …

Background: The importance of prebiotics consumption is increasing all over the world due
to their beneficial effects on health. Production of better prebiotics from endemic plants raises …

The aim of this study was to improve knowledge of the mutational spectrum causing tuberous
sclerosis complex (TSC) in a sample of Mexican patients, given the limited information …

Cystic fibrosis (CF) is an autosomal recessive disorder characterized by chronic pneumopathy,
pancreatic insufficiency, elevated sweat chloride levels and male infertility. It is caused by …

Non‐syndromic cleft lip/palate ( NSCL / P ) is a common congenital defect in M exico.
Periconceptional intake of folic acid ( FA ) may reduce the risk of this malformation. Although the 5,…

Se presentan los criterios para el abordaje diagn�stico inicial de pacientes con alteraciones
en la diferenciaci�n sexual, de acuerdo a los lineamientos del Grupo Para el Estudio del …

Objective: Identify CTNS gene mutations in nephropathic cystinosis Mexican patients.
Subjects and Methods: Eleven patients were included, nine presenting infantile nephropathic …