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M G Bialer

Showing results (11-20 of 25) with videos related to

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Annales De Genetique|January 1, 1996
Characterization of a de novo t(Y;9) (q11.2;q22) by FISH techniqueR A Conte, S M Kleyman, V Klein, et al.
Lancet (London, England)|August 13, 1994
Prenatal diagnosis of Gorlin syndromeM G Bialer, M R Gailani, J A McLaughlin, et al.
American Journal of Medical Genetics|November 1, 1987
Female external genitalia and müllerian duct derivatives in a 46,XY infant with the smith-lemli-Opitz syndromeM G Bialer, V B Penchaszadeh, E Kahn, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Mechanisms of the origin of a G-positive band within the secondary constriction region of human chromosome 9M J Macera, R S Verma, R A Conte, et al.
Archives of Pathology & Laboratory Medicine|January 1, 1982
Wolman's disease: report of a case, with multiple studiesR Miller, M G Bialer, J F Rogers, et al.
Journal of Vascular Surgery|April 18, 1998
Subclavian artery pseudoaneurysm in type IV Ehlers-Danlos syndromeP I Rossi, L A Scher, S G Friedman, et al.
American Journal of Human Genetics|November 30, 2000
AT-rich palindromes mediate the constitutional t(11;22) translocationL Edelmann, E Spiteri, K Koren, et al.
Neurology|February 1, 1995
Mitochondrial encephalomyopathy associated with a single nucleotide pair deletion in the mitochondrial tRNALeu(UUR) geneJ M Shoffner, M G Bialer, S G Pavlakis, et al.
American Journal of Medical Genetics|April 1, 1992
Allan-Herndon-Dudley syndrome: clinical and linkage studies on a second familyM G Bialer, L Lawrence, R E Stevenson, et al.
Prenatal Diagnosis|February 1, 1996
Prenatal diagnosis of mitochondrial fatty acid oxidation defectsM A Nada, C Vianey-Saban, C R Roe, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Annales De Genetique|January 1, 1996
Characterization of a de novo t(Y;9) (q11.2;q22) by FISH techniqueR A Conte, S M Kleyman, V Klein, et al.
Lancet (London, England)|August 13, 1994
Prenatal diagnosis of Gorlin syndromeM G Bialer, M R Gailani, J A McLaughlin, et al.
American Journal of Medical Genetics|November 1, 1987
Female external genitalia and müllerian duct derivatives in a 46,XY infant with the smith-lemli-Opitz syndromeM G Bialer, V B Penchaszadeh, E Kahn, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Mechanisms of the origin of a G-positive band within the secondary constriction region of human chromosome 9M J Macera, R S Verma, R A Conte, et al.
Archives of Pathology & Laboratory Medicine|January 1, 1982
Wolman's disease: report of a case, with multiple studiesR Miller, M G Bialer, J F Rogers, et al.
Journal of Vascular Surgery|April 18, 1998
Subclavian artery pseudoaneurysm in type IV Ehlers-Danlos syndromeP I Rossi, L A Scher, S G Friedman, et al.
American Journal of Human Genetics|November 30, 2000
AT-rich palindromes mediate the constitutional t(11;22) translocationL Edelmann, E Spiteri, K Koren, et al.
Neurology|February 1, 1995
Mitochondrial encephalomyopathy associated with a single nucleotide pair deletion in the mitochondrial tRNALeu(UUR) geneJ M Shoffner, M G Bialer, S G Pavlakis, et al.
American Journal of Medical Genetics|April 1, 1992
Allan-Herndon-Dudley syndrome: clinical and linkage studies on a second familyM G Bialer, L Lawrence, R E Stevenson, et al.
Prenatal Diagnosis|February 1, 1996
Prenatal diagnosis of mitochondrial fatty acid oxidation defectsM A Nada, C Vianey-Saban, C R Roe, et al.
Pageof 3