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Eric Haan

Showing results (11-20 of 75) with videos related to

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American Journal of Medical Genetics. Part A|April 18, 2020
CDH1-related blepharocheilodontic syndrome is associated with diffuse gastric cancer riskShannon LeBlanc, Dildeepa Naveen, Eric Haan, et al.
Pediatrics|April 25, 2007
Upper-limb botulinum toxin A injection and occupational therapy in children with hemiplegic cerebral palsy identified from a population register: a single-blind, randomized, controlled trialRemo N Russo, Maria Crotty, Michelle D Miller, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|March 1, 2012
Cytomegalovirus and Epstein-Barr virus may be associated with some cases of cerebral palsyGai McMichael, Alastair MacLennan, Catherine Gibson, et al.
Australian and New Zealand Journal of Public Health|December 22, 2005
Health professionals' knowledge, practice and opinions about fetal alcohol syndrome and alcohol consumption in pregnancyJan Payne, Elizabeth Elliott, Heather D'Antoine, et al.
Journal of Genetic Counseling|July 23, 2016
Is there a Role for Genetic Counselors in Prenatal Paternity Testing? - an Assessment Based on Audit of 13 years of Clinical Experience in South AustraliaKate E Riley, Hayley Salvemini, Eric Haan, et al.
American Journal of Medical Genetics. Part A|August 3, 2016
Recurrent chronic histiocytic intervillositis with intrauterine growth restriction, osteopenia, and fracturesApril Crawford, Lynette Moore, Gregory Bennett, et al.
BMC Medical Genetics|May 10, 2017
Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome)Shari Javadiyan, Jamie E Craig, Shiwani Sharma, et al.
American Journal of Medical Genetics. Part A|January 28, 2003
Recombinants of intrachromosomal transposition of subtelomeres in chromosomes 1 and 2: a cause of minute terminal chromosomal imbalancesArt Daniel, Elizabeth Baker, Nicole Chia, et al.
European Journal of Medical Genetics|August 6, 2013
NKX2-1 mutation in a family diagnosed with ataxic dyskinetic cerebral palsyGai McMichael, Eric Haan, Alison Gardner, et al.
The Journal of Pediatrics|April 28, 2009
Sporadic in utero generalized edema caused by mutations in the lymphangiogenic genes VEGFR3 and FOXC2Arash Ghalamkarpour, Christian Debauche, Eric Haan, et al.
Pageof 8

Showing results (11-20 of 75) with videos related to

Sort By:
Pageof 8
American Journal of Medical Genetics. Part A|April 18, 2020
CDH1-related blepharocheilodontic syndrome is associated with diffuse gastric cancer riskShannon LeBlanc, Dildeepa Naveen, Eric Haan, et al.
Pediatrics|April 25, 2007
Upper-limb botulinum toxin A injection and occupational therapy in children with hemiplegic cerebral palsy identified from a population register: a single-blind, randomized, controlled trialRemo N Russo, Maria Crotty, Michelle D Miller, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|March 1, 2012
Cytomegalovirus and Epstein-Barr virus may be associated with some cases of cerebral palsyGai McMichael, Alastair MacLennan, Catherine Gibson, et al.
Australian and New Zealand Journal of Public Health|December 22, 2005
Health professionals' knowledge, practice and opinions about fetal alcohol syndrome and alcohol consumption in pregnancyJan Payne, Elizabeth Elliott, Heather D'Antoine, et al.
Journal of Genetic Counseling|July 23, 2016
Is there a Role for Genetic Counselors in Prenatal Paternity Testing? - an Assessment Based on Audit of 13 years of Clinical Experience in South AustraliaKate E Riley, Hayley Salvemini, Eric Haan, et al.
American Journal of Medical Genetics. Part A|August 3, 2016
Recurrent chronic histiocytic intervillositis with intrauterine growth restriction, osteopenia, and fracturesApril Crawford, Lynette Moore, Gregory Bennett, et al.
BMC Medical Genetics|May 10, 2017
Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome)Shari Javadiyan, Jamie E Craig, Shiwani Sharma, et al.
American Journal of Medical Genetics. Part A|January 28, 2003
Recombinants of intrachromosomal transposition of subtelomeres in chromosomes 1 and 2: a cause of minute terminal chromosomal imbalancesArt Daniel, Elizabeth Baker, Nicole Chia, et al.
European Journal of Medical Genetics|August 6, 2013
NKX2-1 mutation in a family diagnosed with ataxic dyskinetic cerebral palsyGai McMichael, Eric Haan, Alison Gardner, et al.
The Journal of Pediatrics|April 28, 2009
Sporadic in utero generalized edema caused by mutations in the lymphangiogenic genes VEGFR3 and FOXC2Arash Ghalamkarpour, Christian Debauche, Eric Haan, et al.
Pageof 8