S. Canún

发表

Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome

S. Subramony, S. Bendahhou, A. George, 2001, Cell.

A de novo heterozygous point mutation in the p63 gene causing the syndrome of ectrodactyly, ectodermal dysplasia and facial clefting

S. Canún, J. Zenteno, G. Pozo, 2004, The British journal of dermatology.

Videonasopharyngoscopy in patients with 22q11.2 deletion syndrome (Shprintzen syndrome).

A. Ysunza, M. Pamplona, S. Canún, 2003, International journal of pediatric otorhinolaryngology.

PCR–PRINS–FISH analysis of structurally abnormal sex chromosomes in eight patients with Turner phenotype

S. Canún, C. Sierra, C. Navarrete, 2001, Clinical genetics.

Microsatellite analysis in Turner syndrome: parental origin of X chromosomes and possible mechanism of formation of abnormal chromosomes.

S. Canún, J. Zenteno, Marisol López, 2002, American journal of medical genetics.

Molecular analysis of mosaicism for two different de novo acrocentric rearrangements demonstrates diversity in Robertsonian translocation formation.

L. Shaffer, S. Page, S. Canún, 1998, American journal of medical genetics.

No mutation in genes of the WNT signaling pathway in patients with Zimmermann-Laband syndrome.

Gabriele Gillessen-Kaesbach, Kerstin Kutsche, Martin Zenker, 2008, Clinical dysmorphology.

Combined trisomy 9 and Ullrich-Turner syndrome in a girl with a 46,X,der(9)t(X;9)(q12;q32) karyotype.

L. Shaffer, S. Canún, O. Mutchinick, 1998, American journal of medical genetics.

Idiopathic multicentric osteolysis with facial anomalies and nephropathy.

A. Carnevale, S. Canún, V. del Castillo, 1987, American journal of medical genetics.

Andersen syndrome autosomal dominant in three generations.

S. Canún, N. Pérez, L. Beirana, 1999, American journal of medical genetics.

Variability between and within laboratories in the analysis of structural chromosomal abnormalities

A. Carnevale, S. Canún, F. Salamanca, 1979, Clinical genetics.

Blepharo-cheilo-dontic (BCD) syndrome in two Mexican patients.

S. Canún, M. Quintana-García, M. H. Valdéz-de la Torre, 1999, American journal of medical genetics.

Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactyly

S. Scherer, L. Tsui, S. Antonarakis, 1998, Human Genetics.