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Bassem A Bejjani

Showing results (41-50 of 71) with videos related to

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American Journal of Medical Genetics|October 12, 2002
Partial deletions of the long arm of chromosome 13 associated with holoprosencephaly and the Dandy-Walker malformationW Michael McCormack, Joseph J Shen, Stacey M Curry, et al.
American Journal of Medical Genetics. Part A|April 18, 2003
Partial deletions of the long arm of chromosome 13 associated with holoprosencephaly and the Dandy-Walker malformationW Michael McCormack, Joseph J Shen, Stacey M Curry, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|November 26, 2009
Greig cephalopolysyndactyly syndrome: diagnosis based on prenatal sonographic features coupled with comparative genomic hybridizationIlan E Timor-Tritsch, Sarah Kapp, Robert Berg, et al.
Investigative Ophthalmology & Visual Science|March 28, 2006
Of mice and men: tyrosinase modification of congenital glaucoma in mice but not in humansCarla Bidinost, Natalie Hernandez, Deepak P Edward, et al.
Carcinogenesis|June 17, 2003
Single amino acid mutations, but not common polymorphisms, decrease the activity of CYP1B1 against (-)benzo[a]pyrene-7R-trans-7,8-dihydrodiolJennifer S Mammen, Gary S Pittman, Ying Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 15, 2009
Impact of genotype-first diagnosis: the detection of microdeletion and microduplication syndromes with cancer predisposition by aCGHSara Anne Adams, Justine Coppinger, Sulagna C Saitta, et al.
American Journal of Medical Genetics. Part A|November 15, 2006
Detection of low-level mosaicism by array CGH in routine diagnostic specimensBlake C Ballif, Emily A Rorem, Kyle Sundin, et al.
Investigative Ophthalmology & Visual Science|March 28, 2006
Heterozygous and homozygous mutations in PITX3 in a large Lebanese family with posterior polar cataracts and neurodevelopmental abnormalitiesCarla Bidinost, Masayuki Matsumoto, Daniel Chung, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2010
Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disordersJill A Rosenfeld, Blake C Ballif, Beth S Torchia, et al.
Molecular Vision|August 19, 2011
Identification of novel suggestive loci for high-grade myopia in Polish familiesMalgorzata Rydzanicz, Swapan K Nath, Celi Sun, et al.
Pageof 8

Showing results (41-50 of 71) with videos related to

Sort By:
Pageof 8
American Journal of Medical Genetics|October 12, 2002
Partial deletions of the long arm of chromosome 13 associated with holoprosencephaly and the Dandy-Walker malformationW Michael McCormack, Joseph J Shen, Stacey M Curry, et al.
American Journal of Medical Genetics. Part A|April 18, 2003
Partial deletions of the long arm of chromosome 13 associated with holoprosencephaly and the Dandy-Walker malformationW Michael McCormack, Joseph J Shen, Stacey M Curry, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|November 26, 2009
Greig cephalopolysyndactyly syndrome: diagnosis based on prenatal sonographic features coupled with comparative genomic hybridizationIlan E Timor-Tritsch, Sarah Kapp, Robert Berg, et al.
Investigative Ophthalmology & Visual Science|March 28, 2006
Of mice and men: tyrosinase modification of congenital glaucoma in mice but not in humansCarla Bidinost, Natalie Hernandez, Deepak P Edward, et al.
Carcinogenesis|June 17, 2003
Single amino acid mutations, but not common polymorphisms, decrease the activity of CYP1B1 against (-)benzo[a]pyrene-7R-trans-7,8-dihydrodiolJennifer S Mammen, Gary S Pittman, Ying Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 15, 2009
Impact of genotype-first diagnosis: the detection of microdeletion and microduplication syndromes with cancer predisposition by aCGHSara Anne Adams, Justine Coppinger, Sulagna C Saitta, et al.
American Journal of Medical Genetics. Part A|November 15, 2006
Detection of low-level mosaicism by array CGH in routine diagnostic specimensBlake C Ballif, Emily A Rorem, Kyle Sundin, et al.
Investigative Ophthalmology & Visual Science|March 28, 2006
Heterozygous and homozygous mutations in PITX3 in a large Lebanese family with posterior polar cataracts and neurodevelopmental abnormalitiesCarla Bidinost, Masayuki Matsumoto, Daniel Chung, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2010
Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disordersJill A Rosenfeld, Blake C Ballif, Beth S Torchia, et al.
Molecular Vision|August 19, 2011
Identification of novel suggestive loci for high-grade myopia in Polish familiesMalgorzata Rydzanicz, Swapan K Nath, Celi Sun, et al.
Pageof 8