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

Jill K Northup

Showing results (1-10 of 8) with videos related to

Pageof 1
Sort By:
American Journal of Medical Genetics. Part A|March 18, 2009
Molecular cytogenetic characterization of an interstitial de novo 13q deletion in a 3-month-old with severe pediatric gastroesophageal refluxNeena L Champaigne, Nicole A Laird, Jill K Northup, et al.
Clinical Dysmorphology|June 24, 2010
Pericentric inversion, inv(14)(p11.2q22.3), in a 9-month old with features of Goldenhar syndromeJill K Northup, Dena Matalon, Judy C Hawkins, et al.
European Journal of Haematology|February 23, 2007
Do cytogenetic abnormalities precede morphologic abnormalities in a developing malignant condition?Jill K Northup, Swarupa A Gadre, Yimin Ge, et al.
American Journal of Medical Genetics. Part A|September 17, 2008
First report of an interstitial deletion, del(5)(q33.1q35.1) in a girl with primary amenorrhea, seizures, and severe behavioral and developmental deficienciesJill K Northup, Kären E Wain, Judy C Hawkins, et al.
European Journal of Medical Genetics|April 7, 2011
A complex chromosome rearrangement, der(6)ins(6)(p21.1q25.3q27)inv(6)(p25.3q27), in a child with cleidocranial dysplasiaJill K Northup, Reuben Matalon, Lillian H Lockhart, et al.
American Journal of Hematology|July 27, 2005
Interphase FISH screening for the LCR-mediated common rearrangement of isochromosome 17q in primary myelofibrosisGabriel A Bien-Willner, Paweł Stankiewicz, James R Lupski, et al.
American Journal of Medical Genetics. Part A|February 28, 2008
Molecular cytogenetic characterization of a unique and complex de novo 8p rearrangementSusanna L Cooke, Jill K Northup, Neena L Champaige, et al.
American Journal of Human Genetics|February 24, 2005
Position effects due to chromosome breakpoints that map approximately 900 Kb upstream and approximately 1.3 Mb downstream of SOX9 in two patients with campomelic dysplasiaGopalrao V N Velagaleti, Gabriel A Bien-Willner, Jill K Northup, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics. Part A|March 18, 2009
Molecular cytogenetic characterization of an interstitial de novo 13q deletion in a 3-month-old with severe pediatric gastroesophageal refluxNeena L Champaigne, Nicole A Laird, Jill K Northup, et al.
Clinical Dysmorphology|June 24, 2010
Pericentric inversion, inv(14)(p11.2q22.3), in a 9-month old with features of Goldenhar syndromeJill K Northup, Dena Matalon, Judy C Hawkins, et al.
European Journal of Haematology|February 23, 2007
Do cytogenetic abnormalities precede morphologic abnormalities in a developing malignant condition?Jill K Northup, Swarupa A Gadre, Yimin Ge, et al.
American Journal of Medical Genetics. Part A|September 17, 2008
First report of an interstitial deletion, del(5)(q33.1q35.1) in a girl with primary amenorrhea, seizures, and severe behavioral and developmental deficienciesJill K Northup, Kären E Wain, Judy C Hawkins, et al.
European Journal of Medical Genetics|April 7, 2011
A complex chromosome rearrangement, der(6)ins(6)(p21.1q25.3q27)inv(6)(p25.3q27), in a child with cleidocranial dysplasiaJill K Northup, Reuben Matalon, Lillian H Lockhart, et al.
American Journal of Hematology|July 27, 2005
Interphase FISH screening for the LCR-mediated common rearrangement of isochromosome 17q in primary myelofibrosisGabriel A Bien-Willner, Paweł Stankiewicz, James R Lupski, et al.
American Journal of Medical Genetics. Part A|February 28, 2008
Molecular cytogenetic characterization of a unique and complex de novo 8p rearrangementSusanna L Cooke, Jill K Northup, Neena L Champaige, et al.
American Journal of Human Genetics|February 24, 2005
Position effects due to chromosome breakpoints that map approximately 900 Kb upstream and approximately 1.3 Mb downstream of SOX9 in two patients with campomelic dysplasiaGopalrao V N Velagaleti, Gabriel A Bien-Willner, Jill K Northup, et al.
Pageof 1