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Mayo Clinic Proceedings|January 13, 2001
Application of multicolor fluorescent in situ hybridization for enhanced characterization of chromosomal abnormalities in congenital disordersS M Jalal, M E Law, N M Lindor, et al.American Journal of Medical Genetics|April 1, 1993
Method for sequential staining of GTL-banded metaphases with fluorescent-labeled chromosome-specific paint probesS M Jalal, M E Law, E R Christensen, et al.American Journal of Medical Genetics|December 18, 1998
Visual impairment due to macular disciform scars in a 20-year-old man with Smith-Magenis syndrome: another ophthalmologic complicationD Babovic-Vuksanovic, S M Jalal, J A Garrity, et al.Clinical Genetics|June 4, 1998
Maternal cell contamination of buccal smear samples in nursing neonatesD Babovic-Vuksanovic, V V Michels, M E Law, et al.American Journal of Medical Genetics|December 26, 2001
Tandem translocation of chromosomes 22 and 15 with two preserved satellite stalk regions and deletion 22q13.3-qterK A Lee, S H Kim, M H Lee, et al.Journal of Medical Genetics|February 1, 1978
Trisomy 18 syndrome with an unusual karyotype: possible double isochromosomeL M Larson, W A Wasdahl, J H Saumur, et al.Prenatal Diagnosis|March 1, 2000
Inherited interstitial deletion of chromosomes 5p and 16q without apparent phenotypic effect: further confirmationJ L Hand, V V Michels, M J Marinello, et al.Annales De Genetique|January 1, 1988
Complete trisomy 17p a relatively new syndromeJ T Martsolf, L Larson, S M Jalal, et al.Mayo Clinic Proceedings|December 1, 1995
DNA fluorescent probes for diagnosis of velocardiofacial and related syndromesP A Crifasi, V V Michels, D J Driscoll, et al.American Journal of Medical Genetics|December 1, 1988
Direct chromosome analysis from neonatal cord bloodD W Day, S M Jalal, L Sinclair-Worley, et al.Pageof 8