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Joe J Hoo

Showing results (1-10 of 11) with videos related to

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American Journal of Medical Genetics. Part A|December 12, 2002
Two sibs with brachyolmia type Hobaek: five year follow-up through pubertyJoe J Hoo, Michael Oliphant
American Journal of Medical Genetics. Part A|July 22, 2004
Is brachydactyly type Ballard a variant of brachydactyly type E?Kimberly Jensen, Joe J Hoo
American Journal of Medical Genetics. Part A|November 20, 2004
Familial hyper- and hypopigmentation with age-related pattern changeJoe J Hoo, Antony E Shrimpton
American Journal of Medical Genetics. Part A|January 19, 2008
Distal 3p deletion is not necessarily associated with dysmorphic features or psychomotor delayJoe J Hoo, Antony E Shrimpton
Pediatrics|March 3, 2006
Difficulty in recognizing multiple sulfatase deficiency in an infantRoberto P Santos, Joe J Hoo
European Journal of Medical Genetics|February 25, 2006
A TNNI2 mutation in a family with distal arthrogryposis type 2BAntony E Shrimpton, Joe J Hoo
American Journal of Medical Genetics. Part A|March 14, 2007
"Zwilling" versus "Tai Chi" configuration of double-sized ring chromosomeJoe J Hoo, Constance K Stein
American Journal of Medical Genetics. Part A|January 18, 2006
Karyotype-phenotype analysis and molecular delineation of a 3p26 deletion/8q24.3 duplication case with a virtually normal phenotype and mild cognitive deficitAntony E Shrimpton, Kimberly A Jensen, Joe J Hoo
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 26, 2009
FG syndrome, an X-linked multiple congenital anomaly syndrome: the clinical phenotype and an algorithm for diagnostic testingRobin Dawn Clark, John M Graham, Michael J Friez, et al.
European Journal of Human Genetics : EJHG|January 21, 2011
Deletions flanked by breakpoints 3 and 4 on 15q13 may contribute to abnormal phenotypesJill A Rosenfeld, Lindsey E Stephens, Justine Coppinger, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
American Journal of Medical Genetics. Part A|December 12, 2002
Two sibs with brachyolmia type Hobaek: five year follow-up through pubertyJoe J Hoo, Michael Oliphant
American Journal of Medical Genetics. Part A|July 22, 2004
Is brachydactyly type Ballard a variant of brachydactyly type E?Kimberly Jensen, Joe J Hoo
American Journal of Medical Genetics. Part A|November 20, 2004
Familial hyper- and hypopigmentation with age-related pattern changeJoe J Hoo, Antony E Shrimpton
American Journal of Medical Genetics. Part A|January 19, 2008
Distal 3p deletion is not necessarily associated with dysmorphic features or psychomotor delayJoe J Hoo, Antony E Shrimpton
Pediatrics|March 3, 2006
Difficulty in recognizing multiple sulfatase deficiency in an infantRoberto P Santos, Joe J Hoo
European Journal of Medical Genetics|February 25, 2006
A TNNI2 mutation in a family with distal arthrogryposis type 2BAntony E Shrimpton, Joe J Hoo
American Journal of Medical Genetics. Part A|March 14, 2007
"Zwilling" versus "Tai Chi" configuration of double-sized ring chromosomeJoe J Hoo, Constance K Stein
American Journal of Medical Genetics. Part A|January 18, 2006
Karyotype-phenotype analysis and molecular delineation of a 3p26 deletion/8q24.3 duplication case with a virtually normal phenotype and mild cognitive deficitAntony E Shrimpton, Kimberly A Jensen, Joe J Hoo
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 26, 2009
FG syndrome, an X-linked multiple congenital anomaly syndrome: the clinical phenotype and an algorithm for diagnostic testingRobin Dawn Clark, John M Graham, Michael J Friez, et al.
European Journal of Human Genetics : EJHG|January 21, 2011
Deletions flanked by breakpoints 3 and 4 on 15q13 may contribute to abnormal phenotypesJill A Rosenfeld, Lindsey E Stephens, Justine Coppinger, et al.
Pageof 2