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Clinical Genetics|September 1, 1991
Enhancement of amniotic fluid cell growth for genetic amniocentesisT Mathews, R S VermaGenetica|January 1, 1992
Evolution of pericentromeric heterochromatin of human X chromosomeS Luke, T Mathews, R S VermaGynecologic and Obstetric Investigation|January 1, 1992
Prenatal cytogenetic diagnosis of 1,400 consecutive amniocentesesT Mathews, D Navsaria, R S VermaCytobios|January 1, 1994
In situ nick translation of human chromosomes with the restriction endonuclease Pvu II [5' CAG decreases CTG 3']T Mathews, A K Agarwal, R S VermaHistochemistry|January 1, 1989
Restriction endonuclease AluI resistant chromatin of "aged" slidesA Agarwal, T Mathews, V Sindwani, et al.Human Heredity|May 1, 1993
Chromosomal anomalies in 1,000 children referred with suspected genetic disordersD Navsaria, T Mathews, R A Conte, et al.Journal of Cell Science|December 1, 1992
Molecular characterization of the secondary constriction region (qh) of human chromosome 9 with pericentric inversionS Luke, R S Verma, R A Conte, et al.Gynecologic and Obstetric Investigation|January 1, 1994
Monozygotic twinning in a female with triple X[47,XXX]R S Verma, R A Conte, T Mathews, et al.Genetic Analysis, Techniques and Applications|October 1, 1992
Molecular characterization of the smallest secondary constriction region (qh) of human chromosome 16R S Verma, S Luke, T Mathews, et al.Clinical Genetics|August 1, 1996
Molecular characterization of 21p- variant chromosomeR A Conte, T Mathews, S M Kleyman, et al.Pageof 38