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J L Frias

Showing results (61-70 of 71) with videos related to

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American Journal of Medical Genetics|June 1, 1990
Partial duplication 1q: report of four patients and review of the literatureS A Rasmussen, J L Frias, C Z Lafer, et al.
American Journal of Medical Genetics. Supplement|January 1, 1990
Clinical, cytogenetic, and molecular evaluation of a patient with partial trisomy 21 (21q11-q22) lacking the classical Down syndrome phenotypeC A Williams, J L Frias, M K McCormick, et al.
Southern Medical Journal|February 1, 1982
Evaluation of a Tay-Sachs screening program on a college campusJ P Krischer, T L Savitt, A Spring, et al.
Skeletal Radiology|January 1, 1991
Radiographic features of craniometadiaphyseal dysplasia, wormian bone typeL O Langer, P W Brill, E Afshani, et al.
American Journal of Medical Genetics|January 1, 1978
Normal intelligence in two children with Carpenter syndromeJ L Frias, A H Felman, A L Rosenbloom, et al.
American Journal of Medical Genetics|September 1, 1986
Isolated and syndromic cryptophthalmosI T Thomas, J L Frias, V Felix, et al.
American Journal of Human Genetics|August 1, 1989
Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerismI T Thomas, J L Frias, E S Cantu, et al.
Journal of Medical Genetics|August 1, 1994
Facial morphometry of Ecuadorian patients with growth hormone receptor deficiency/Laron syndromeG B Schaefer, A L Rosenbloom, J Guevara-Aguirre, et al.
Clinical Genetics|September 1, 1996
Neuroradiology and clinical aspects of Usher syndromeM L Tamayo, C Maldonado, S L Plaza, et al.
Clinical Genetics|October 1, 1991
Usher syndrome: results of a screening program in ColombiaM L Tamayo, J E Bernal, G E Tamayo, et al.
Pageof 8

Showing results (61-70 of 71) with videos related to

Sort By:
Pageof 8
American Journal of Medical Genetics|June 1, 1990
Partial duplication 1q: report of four patients and review of the literatureS A Rasmussen, J L Frias, C Z Lafer, et al.
American Journal of Medical Genetics. Supplement|January 1, 1990
Clinical, cytogenetic, and molecular evaluation of a patient with partial trisomy 21 (21q11-q22) lacking the classical Down syndrome phenotypeC A Williams, J L Frias, M K McCormick, et al.
Southern Medical Journal|February 1, 1982
Evaluation of a Tay-Sachs screening program on a college campusJ P Krischer, T L Savitt, A Spring, et al.
Skeletal Radiology|January 1, 1991
Radiographic features of craniometadiaphyseal dysplasia, wormian bone typeL O Langer, P W Brill, E Afshani, et al.
American Journal of Medical Genetics|January 1, 1978
Normal intelligence in two children with Carpenter syndromeJ L Frias, A H Felman, A L Rosenbloom, et al.
American Journal of Medical Genetics|September 1, 1986
Isolated and syndromic cryptophthalmosI T Thomas, J L Frias, V Felix, et al.
American Journal of Human Genetics|August 1, 1989
Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerismI T Thomas, J L Frias, E S Cantu, et al.
Journal of Medical Genetics|August 1, 1994
Facial morphometry of Ecuadorian patients with growth hormone receptor deficiency/Laron syndromeG B Schaefer, A L Rosenbloom, J Guevara-Aguirre, et al.
Clinical Genetics|September 1, 1996
Neuroradiology and clinical aspects of Usher syndromeM L Tamayo, C Maldonado, S L Plaza, et al.
Clinical Genetics|October 1, 1991
Usher syndrome: results of a screening program in ColombiaM L Tamayo, J E Bernal, G E Tamayo, et al.
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