Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

A J M Hoogeboom

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

Pageof 1
Sort By:
Genetic Counseling (Geneva, Switzerland)|August 11, 2012
X-linked Aarskog syndrome: report on a novel FGD1 gene mutation. Executive dysfunction as part of the behavioural phenotypeW M A Verhoeven, J I M Egger, A J M Hoogeboom
Nederlands Tijdschrift Voor Tandheelkunde|March 11, 2008
[Genetics of craniofacial development]L N A van Adrichem, A J M Hoogeboom, E B Wolvius
American Journal of Medical Genetics. Part A|July 17, 2008
Deletion of 1 amino acid in Indian hedgehog leads to brachydactylyA1E M Lodder, A J M Hoogeboom, J H Coert, et al.
Clinical Genetics|April 22, 2004
Deletion of the TWIST gene in a large five-generation familyI M De Heer, A J M Hoogeboom, H J Eussen, et al.
Nederlands Tijdschrift Voor Geneeskunde|February 1, 2002
[From gene to disease; craniosynostosis syndromes due to FGFR2-mutation]C M A van Ravenswaaij-Arts, A M W van den Ouweland, A J M Hoogeboom, et al.
International Journal of Oral and Maxillofacial Surgery|June 18, 2020
Undetected anomalies in foetuses with a prenatal diagnosis of isolated cleftM Haj, M J Koudstaal, M S Ramcharan, et al.
American Journal of Medical Genetics. Part A|April 27, 2004
Early diagnosis of Wolf-Hirschhorn syndrome triggered by a life-threatening event: congenital diaphragmatic herniaM F van Dooren, A S Brooks, A J M Hoogeboom, et al.
European Journal of Human Genetics : EJHG|November 28, 2013
Phenotypes of craniofrontonasal syndrome in patients with a pathogenic mutation in EFNB1M E P van den Elzen, S R F Twigg, J A C Goos, et al.
Journal of Plastic, Reconstructive & Aesthetic Surgery : JPRAS|November 17, 2009
Long-term functional outcome in 167 patients with syndromic craniosynostosis; defining a syndrome-specific risk profileT de Jong, N Bannink, H H Bredero-Boelhouwer, et al.
European Journal of Medical Genetics|June 24, 2017
NGS panel analysis in 24 ectopia lentis patients; a clinically relevant test with a high diagnostic yieldE Overwater, K Floor, D van Beek, et al.
Pageof 1

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

Sort By:
Pageof 1
Genetic Counseling (Geneva, Switzerland)|August 11, 2012
X-linked Aarskog syndrome: report on a novel FGD1 gene mutation. Executive dysfunction as part of the behavioural phenotypeW M A Verhoeven, J I M Egger, A J M Hoogeboom
Nederlands Tijdschrift Voor Tandheelkunde|March 11, 2008
[Genetics of craniofacial development]L N A van Adrichem, A J M Hoogeboom, E B Wolvius
American Journal of Medical Genetics. Part A|July 17, 2008
Deletion of 1 amino acid in Indian hedgehog leads to brachydactylyA1E M Lodder, A J M Hoogeboom, J H Coert, et al.
Clinical Genetics|April 22, 2004
Deletion of the TWIST gene in a large five-generation familyI M De Heer, A J M Hoogeboom, H J Eussen, et al.
Nederlands Tijdschrift Voor Geneeskunde|February 1, 2002
[From gene to disease; craniosynostosis syndromes due to FGFR2-mutation]C M A van Ravenswaaij-Arts, A M W van den Ouweland, A J M Hoogeboom, et al.
International Journal of Oral and Maxillofacial Surgery|June 18, 2020
Undetected anomalies in foetuses with a prenatal diagnosis of isolated cleftM Haj, M J Koudstaal, M S Ramcharan, et al.
American Journal of Medical Genetics. Part A|April 27, 2004
Early diagnosis of Wolf-Hirschhorn syndrome triggered by a life-threatening event: congenital diaphragmatic herniaM F van Dooren, A S Brooks, A J M Hoogeboom, et al.
European Journal of Human Genetics : EJHG|November 28, 2013
Phenotypes of craniofrontonasal syndrome in patients with a pathogenic mutation in EFNB1M E P van den Elzen, S R F Twigg, J A C Goos, et al.
Journal of Plastic, Reconstructive & Aesthetic Surgery : JPRAS|November 17, 2009
Long-term functional outcome in 167 patients with syndromic craniosynostosis; defining a syndrome-specific risk profileT de Jong, N Bannink, H H Bredero-Boelhouwer, et al.
European Journal of Medical Genetics|June 24, 2017
NGS panel analysis in 24 ectopia lentis patients; a clinically relevant test with a high diagnostic yieldE Overwater, K Floor, D van Beek, et al.
Pageof 1