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

J J Engelen

Showing results (31-40 of 49) with videos related to

Pageof 5
Sort By:
Genetic Counseling (Geneva, Switzerland)|April 11, 2000
Prenatally detected marker chromosome identified as an i(22)(p10) using (micro)FISHJ J Engelen, J H Tuerlings, J C Albrechts, et al.
Genetic Counseling (Geneva, Switzerland)|October 24, 2000
De novo translocation (2;18)(q21;q22) in a child with severe epilepsy, developmental delay and mild dysmorphismM Bal, C T Schrander-Stumpel, L E Meers, et al.
Journal of Medical Genetics|July 1, 1996
Disclosure of five breakpoints in a complex chromosome rearrangement by microdissection and FISHJ J Engelen, W J Loots, J C Albrechts, et al.
Genetic Counseling (Geneva, Switzerland)|April 16, 2004
Hereditary motor and sensory neuropathy (HMSN) IA, developmental delay and autism related disorder in a boy with duplication (17)(p11.2p12)U Moog, J J Engelen, B W Weber, et al.
American Journal of Medical Genetics|June 22, 2000
Severe phenotypes associated with inactive ring X chromosomesB R Migeon, M Ausems, J Giltay, et al.
Genetic Counseling (Geneva, Switzerland)|November 6, 2001
Holoprosencephaly: the Maastricht experienceU Moog, C E De Die-Smulders, C T Schrander-Stumpel, et al.
Genetic Counseling (Geneva, Switzerland)|July 28, 1999
Duplication within chromosome region 15q11-q13 in a patient with similarities to Prader-Willi syndrome confirmed by region-specific and band-specific fishJ J Engelen, W J Loots, J C Albrechts, et al.
American Journal of Medical Genetics|May 5, 2001
De novo duplication (5)(q31.3q33.3): report of a patient and characterization of the duplicated region using microdissection and FISHJ F Sanchez-Garcia, C E de Die-Smulders, J W Weber, et al.
Genetic Counseling (Geneva, Switzerland)|January 5, 2001
Trisomy 7p: report of 2 patients and literature reviewY H Arens, A Toutain, J J Engelen, et al.
Clinical Genetics|December 1, 1994
Partial trisomy of the short arm of chromosome 18 due to inversion duplication and direct duplicationU Moog, J J Engelen, C E de Die-Smulders, et al.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
Genetic Counseling (Geneva, Switzerland)|April 11, 2000
Prenatally detected marker chromosome identified as an i(22)(p10) using (micro)FISHJ J Engelen, J H Tuerlings, J C Albrechts, et al.
Genetic Counseling (Geneva, Switzerland)|October 24, 2000
De novo translocation (2;18)(q21;q22) in a child with severe epilepsy, developmental delay and mild dysmorphismM Bal, C T Schrander-Stumpel, L E Meers, et al.
Journal of Medical Genetics|July 1, 1996
Disclosure of five breakpoints in a complex chromosome rearrangement by microdissection and FISHJ J Engelen, W J Loots, J C Albrechts, et al.
Genetic Counseling (Geneva, Switzerland)|April 16, 2004
Hereditary motor and sensory neuropathy (HMSN) IA, developmental delay and autism related disorder in a boy with duplication (17)(p11.2p12)U Moog, J J Engelen, B W Weber, et al.
American Journal of Medical Genetics|June 22, 2000
Severe phenotypes associated with inactive ring X chromosomesB R Migeon, M Ausems, J Giltay, et al.
Genetic Counseling (Geneva, Switzerland)|November 6, 2001
Holoprosencephaly: the Maastricht experienceU Moog, C E De Die-Smulders, C T Schrander-Stumpel, et al.
Genetic Counseling (Geneva, Switzerland)|July 28, 1999
Duplication within chromosome region 15q11-q13 in a patient with similarities to Prader-Willi syndrome confirmed by region-specific and band-specific fishJ J Engelen, W J Loots, J C Albrechts, et al.
American Journal of Medical Genetics|May 5, 2001
De novo duplication (5)(q31.3q33.3): report of a patient and characterization of the duplicated region using microdissection and FISHJ F Sanchez-Garcia, C E de Die-Smulders, J W Weber, et al.
Genetic Counseling (Geneva, Switzerland)|January 5, 2001
Trisomy 7p: report of 2 patients and literature reviewY H Arens, A Toutain, J J Engelen, et al.
Clinical Genetics|December 1, 1994
Partial trisomy of the short arm of chromosome 18 due to inversion duplication and direct duplicationU Moog, J J Engelen, C E de Die-Smulders, et al.
Pageof 5