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M J Pettenati

Showing results (31-40 of 87) with videos related to

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Journal of Forensic Sciences|November 1, 1996
Gender identification of human hair using fluorescence in situ hybridizationJ A Prahlow, P E Lantz, K Cox-Jones, et al.
Human Molecular Genetics|April 18, 1998
Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndromeJ A Price, D W Bowden, J T Wright, et al.
American Journal of Medical Genetics|March 1, 1993
Inversion (X)(p11.4q22) associated with Norrie disease in a four generation familyM J Pettenati, P N Rao, R G Weaver, et al.
American Journal of Hematology|September 1, 1988
Acute lymphoblastic leukemia in a patient with longstanding polycythemia vera: cytogenetic analysis reveals two distinct abnormal clonesJ Anastasi, M J Pettenati, M M Le Beau, et al.
Prenatal Diagnosis|March 12, 1999
Prenatal interphase detection by FISH of a sex chromosome mosaicism when cytogenetics reports a pseudomosaicismM J Pettenati, M N Berry, P S Hart, et al.
Genomics|May 8, 1998
Characterization of human and mouse rod cGMP phosphodiesterase delta subunit (PDE6D) and chromosomal localization of the human geneN Li, S K Florio, M J Pettenati, et al.
American Journal of Human Genetics|June 13, 1998
Genetic linkage of hereditary gingival fibromatosis to chromosome 2p21T C Hart, D Pallos, D W Bowden, et al.
American Journal of Medical Genetics|December 1, 1993
Blepharophimosis, ptosis, and epicanthus inversus syndrome (BPES) associated with interstitial deletion of band 3q22: review and gene assignment to the interface of band 3q22.3 and 3q23T Jewett, P N Rao, R G Weaver, et al.
Human Genetics|August 1, 1992
Molecular cytogenetic analysis of a familial 8p23.1 deletion associated with minimal dysmorphic features, seizures, and mild mental retardationM J Pettenati, N Rao, C Johnson, et al.
Gene|March 16, 2000
Analysis of the human LHX3 neuroendocrine transcription factor gene and mapping to the subtelomeric region of chromosome 9K W Sloop, A D Showalter, C Von Kap-Herr, et al.
Pageof 9

Showing results (31-40 of 87) with videos related to

Sort By:
Pageof 9
Journal of Forensic Sciences|November 1, 1996
Gender identification of human hair using fluorescence in situ hybridizationJ A Prahlow, P E Lantz, K Cox-Jones, et al.
Human Molecular Genetics|April 18, 1998
Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndromeJ A Price, D W Bowden, J T Wright, et al.
American Journal of Medical Genetics|March 1, 1993
Inversion (X)(p11.4q22) associated with Norrie disease in a four generation familyM J Pettenati, P N Rao, R G Weaver, et al.
American Journal of Hematology|September 1, 1988
Acute lymphoblastic leukemia in a patient with longstanding polycythemia vera: cytogenetic analysis reveals two distinct abnormal clonesJ Anastasi, M J Pettenati, M M Le Beau, et al.
Prenatal Diagnosis|March 12, 1999
Prenatal interphase detection by FISH of a sex chromosome mosaicism when cytogenetics reports a pseudomosaicismM J Pettenati, M N Berry, P S Hart, et al.
Genomics|May 8, 1998
Characterization of human and mouse rod cGMP phosphodiesterase delta subunit (PDE6D) and chromosomal localization of the human geneN Li, S K Florio, M J Pettenati, et al.
American Journal of Human Genetics|June 13, 1998
Genetic linkage of hereditary gingival fibromatosis to chromosome 2p21T C Hart, D Pallos, D W Bowden, et al.
American Journal of Medical Genetics|December 1, 1993
Blepharophimosis, ptosis, and epicanthus inversus syndrome (BPES) associated with interstitial deletion of band 3q22: review and gene assignment to the interface of band 3q22.3 and 3q23T Jewett, P N Rao, R G Weaver, et al.
Human Genetics|August 1, 1992
Molecular cytogenetic analysis of a familial 8p23.1 deletion associated with minimal dysmorphic features, seizures, and mild mental retardationM J Pettenati, N Rao, C Johnson, et al.
Gene|March 16, 2000
Analysis of the human LHX3 neuroendocrine transcription factor gene and mapping to the subtelomeric region of chromosome 9K W Sloop, A D Showalter, C Von Kap-Herr, et al.
Pageof 9