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M W Steele

Showing results (41-50 of 68) with videos related to

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Annales De Genetique|January 1, 1994
Cytogenetic characterization of cat eye syndrome marker chromosomeS L Wenger, U Surti, N A Nwokoro, et al.
Clinical Genetics|January 1, 1984
The level of 6-phosphogluconate dehydrogenase (6-PGD) activity in a patient with 1p terminal deletion suggests that the gene locus is not distal to sub-band p36.3 on chromosome 1M W Steele, S L Wenger, L O Geweke, et al.
Clinical Genetics|May 1, 1976
Trisomy of chromosome 20S F Pan, S R Fatora, J E Haas, et al.
American Journal of Medical Genetics|January 1, 1990
Chromosome mosaicism in hypomelanosis of ItoC L Ritter, M W Steele, S L Wenger, et al.
American Journal of Medical Genetics|May 16, 1997
Inherited unbalanced subtelomeric translocation in a child with 8p- and Angelman syndromesS L Wenger, S L Sell, M J Painter, et al.
Clinical Genetics|July 1, 1986
Relative reliability of three different discriminant analysis methods for detecting PKU gene carriersS L Wenger, P W Vieira, J M Breck, et al.
The Journal of Pediatrics|February 1, 1982
Recurrence risk in 21q/21q translocation of Down syndromeK L Garver, S G Marchese, M W Steele, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|May 1, 1989
The fragile X marker and autism in perspectiveJ B Payton, M W Steele, S L Wenger, et al.
American Journal of Medical Genetics|February 27, 1995
Chromosomal abnormalities in a psychiatric populationK E Lewis, M J Lubetsky, S L Wenger, et al.
Ophthalmic Paediatrics and Genetics|March 1, 1993
Broad-spectrum Möbius syndrome associated with a 1;11 chromosome translocationS P Donahue, S L Wenger, M W Steele, et al.
Pageof 7

Showing results (41-50 of 68) with videos related to

Sort By:
Pageof 7
Annales De Genetique|January 1, 1994
Cytogenetic characterization of cat eye syndrome marker chromosomeS L Wenger, U Surti, N A Nwokoro, et al.
Clinical Genetics|January 1, 1984
The level of 6-phosphogluconate dehydrogenase (6-PGD) activity in a patient with 1p terminal deletion suggests that the gene locus is not distal to sub-band p36.3 on chromosome 1M W Steele, S L Wenger, L O Geweke, et al.
Clinical Genetics|May 1, 1976
Trisomy of chromosome 20S F Pan, S R Fatora, J E Haas, et al.
American Journal of Medical Genetics|January 1, 1990
Chromosome mosaicism in hypomelanosis of ItoC L Ritter, M W Steele, S L Wenger, et al.
American Journal of Medical Genetics|May 16, 1997
Inherited unbalanced subtelomeric translocation in a child with 8p- and Angelman syndromesS L Wenger, S L Sell, M J Painter, et al.
Clinical Genetics|July 1, 1986
Relative reliability of three different discriminant analysis methods for detecting PKU gene carriersS L Wenger, P W Vieira, J M Breck, et al.
The Journal of Pediatrics|February 1, 1982
Recurrence risk in 21q/21q translocation of Down syndromeK L Garver, S G Marchese, M W Steele, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|May 1, 1989
The fragile X marker and autism in perspectiveJ B Payton, M W Steele, S L Wenger, et al.
American Journal of Medical Genetics|February 27, 1995
Chromosomal abnormalities in a psychiatric populationK E Lewis, M J Lubetsky, S L Wenger, et al.
Ophthalmic Paediatrics and Genetics|March 1, 1993
Broad-spectrum Möbius syndrome associated with a 1;11 chromosome translocationS P Donahue, S L Wenger, M W Steele, et al.
Pageof 7