Frances Stock
Merida, L, Bolivarian Republic of Venezuela
Last Updated: 09/26/2026
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Found 10 publications
Silver-Russell syndrome. Clinical and etiopathological aspects of a model genomic imprinting entity.
Silver-Russell syndrome. Clinical and etiopathological aspects of a model genomic imprinting entity.
Journal: Archivos argentinos de pediatria
Published: April 17, 2019
Hallazgos clínicos y epidemiológicos en la neurofibromatosis tipo 1 y el complejo esclerosis tuberosa en una serie de pacientes pediátricos
Journal: Boletin medico del Hospital Infantil de Mexico
Published: September 26, 2018
Clinical and molecular study in a family with multiple osteochondromatosis
Journal: Acta ortopedica mexicana
Published: September 06, 2018
Two novel mutations in the TSC2 gene causing severe phenotype in nervous system and skin in a patient with tuberous sclerosis complex.
Journal: Journal of the European Academy of Dermatology and Venereology : JEADV
Published: December 22, 2017
Beckwith-Wiedemann syndrome: clinical and etiopathogenic aspects of a model genomic imprinting entity.
Journal: Archivos argentinos de pediatria
Published: October 18, 2017
Mosaic trisomy 18. Series of cases
Journal: Archivos argentinos de pediatria
Published: October 25, 2016
Gastrointestinal obstruction in the mosaic trisomy X
Journal: Acta gastroenterologica Latinoamericana
Published: September 11, 2015
Clinical and molecular findings of pachyonychia congenita type 2 (PC-2)
Journal: Gaceta medica de Mexico
Published: May 07, 2015
Double mutant alleles in the EXT1 gene not previously reported in a teenager with hereditary multiple exostoses
Journal: Archivos argentinos de pediatria
Published: August 29, 2014
Clinical and molecular study of the Noonan syndrome
Journal: Investigacion clinica
Published: March 22, 2013
Showing 1-10 of 10
Last Updated: 09/26/2026