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K Wisniewski

Showing results (41-50 of 67) with videos related to

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Pediatric Neurology|November 1, 1986
Farber lipogranulomatosis: an unusual presentation in a black childL Eviatar, S L Sklower, K Wisniewski, et al.
Neoplasma|January 1, 1989
Detection of blood group A antigen expression in human colon cancer using monoclonal antibodies with different specificitiesJ Vanák, D Drímalová, O Smyslová, et al.
Clinical Genetics|February 1, 1983
Monosomy 21 syndrome: further delineation including clinical, neuropathological, cytogenetic and biochemical studiesK Wisniewski, M Dambska, E C Jenkins, et al.
Annals of Neurology|March 1, 1985
Adrenoleukomyeloneuropathy with onset in early childhoodN L Rosen, R Lechtenberg, K Wisniewski, et al.
Casopis Lekaru Ceskych|March 18, 1988
[Use of monoclonal antibodies in the detection of blood group antigens A and B in the mucosa of the large intestine]J Vanák, J Ehrmann, D Drímalová, et al.
American Journal of Human Genetics|January 1, 1984
Verbal vs. nonverbal ability, fragile X syndrome, and heterozygous carriersC M Miezejeski, E C Jenkins, A L Hill, et al.
Neuropediatrics|August 1, 1985
Cystathionine disappearance with neuronal loss: a possible neuronal markerK Wisniewski, J A Sturman, E Devine, et al.
Lancet (London, England)|May 28, 1983
Testicular size in fetal fragile X syndromeR D Rudelli, E C Jenkins, K Wisniewski, et al.
American Journal of Clinical Pathology|February 20, 2015
Effectiveness of multiple initiatives to reduce blood component wastageRyan A Collins, Mary K Wisniewski, Jonathan H Waters, et al.
Journal of Autism and Developmental Disorders|September 1, 1982
Autism is associated with the fragile-X syndromeW T Brown, E C Jenkins, E Friedman, et al.
Pageof 7

Showing results (41-50 of 67) with videos related to

Sort By:
Pageof 7
Pediatric Neurology|November 1, 1986
Farber lipogranulomatosis: an unusual presentation in a black childL Eviatar, S L Sklower, K Wisniewski, et al.
Neoplasma|January 1, 1989
Detection of blood group A antigen expression in human colon cancer using monoclonal antibodies with different specificitiesJ Vanák, D Drímalová, O Smyslová, et al.
Clinical Genetics|February 1, 1983
Monosomy 21 syndrome: further delineation including clinical, neuropathological, cytogenetic and biochemical studiesK Wisniewski, M Dambska, E C Jenkins, et al.
Annals of Neurology|March 1, 1985
Adrenoleukomyeloneuropathy with onset in early childhoodN L Rosen, R Lechtenberg, K Wisniewski, et al.
Casopis Lekaru Ceskych|March 18, 1988
[Use of monoclonal antibodies in the detection of blood group antigens A and B in the mucosa of the large intestine]J Vanák, J Ehrmann, D Drímalová, et al.
American Journal of Human Genetics|January 1, 1984
Verbal vs. nonverbal ability, fragile X syndrome, and heterozygous carriersC M Miezejeski, E C Jenkins, A L Hill, et al.
Neuropediatrics|August 1, 1985
Cystathionine disappearance with neuronal loss: a possible neuronal markerK Wisniewski, J A Sturman, E Devine, et al.
Lancet (London, England)|May 28, 1983
Testicular size in fetal fragile X syndromeR D Rudelli, E C Jenkins, K Wisniewski, et al.
American Journal of Clinical Pathology|February 20, 2015
Effectiveness of multiple initiatives to reduce blood component wastageRyan A Collins, Mary K Wisniewski, Jonathan H Waters, et al.
Journal of Autism and Developmental Disorders|September 1, 1982
Autism is associated with the fragile-X syndromeW T Brown, E C Jenkins, E Friedman, et al.
Pageof 7