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

Susan Bint

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

Pageof 1
Sort By:
American Journal of Medical Genetics. Part A|October 15, 2011
Tissue-specific mosaicism for tetrasomy 9p uncovered by array CGHMarwa I Shehab, Inas Mazen, Susan Bint
Journal of Visualized Experiments : Jove|March 6, 2015
Array comparative genomic hybridization (array CGH) for detection of genomic copy number variantsJoo Wook Ahn, Michael Coldwell, Susan Bint, et al.
American Journal of Medical Genetics. Part A|April 6, 2006
Multicolor banding detects a complex three chromosome, seven breakpoint unbalanced rearrangement in an ICSI-derived fetus with multiple abnormalitiesMary J Seller, Susan Bint, Fred Kavalier, et al.
European Journal of Human Genetics : EJHG|September 27, 2003
Class II neocentromeres: a putative common neocentromere site in band 4q21.2Pamela C Warburton, Julian Barwell, Miranda Splitt, et al.
Molecular Cytogenetics|April 9, 2013
Array CGH as a first line diagnostic test in place of karyotyping for postnatal referrals - results from four years' clinical application for over 8,700 patientsJoo Wook Ahn, Susan Bint, Anne Bergbaum, et al.
European Journal of Medical Genetics|August 5, 2008
M-banding characterization of a 16p11.2p13.1 tandem duplication in a child with autism, neurodevelopmental delay and dysmorphismFarkhondeh Behjati, Yousef Shafaghati, Saghar Ghasemi Firouzabadi, et al.
Peerj|May 6, 2014
A new direction for prenatal chromosome microarray testing: software-targeting for detection of clinically significant chromosome imbalance without equivocal findingsJoo Wook Ahn, Susan Bint, Melita D Irving, et al.
Prenatal Diagnosis|December 13, 2024
Advances and Challenges in Prenatal Detection and Genetic Diagnosis of Upper Limb Anomalies: Analysis of a South London and Kent CohortFederica Ruscitti, Tara Giacchino, Lemonia Koutoulas, et al.
Hormone Research in Paediatrics|November 4, 2019
Xq27.1 Duplication Encompassing SOX3: Variable Phenotype and Smallest Duplication Associated with Hypopituitarism to Date - A Large Case Series of Unrelated Patients and a Literature ReviewVed Bhushan Arya, Garima Chawla, Aparna K R Nambisan, et al.
European Journal of Endocrinology|October 15, 2020
Rare CNVs provide novel insights into the molecular basis of GH and IGF-1 insensitivityEmily Cottrell, Claudia P Cabrera, Miho Ishida, et al.
Pageof 1

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

Sort By:
Pageof 1
American Journal of Medical Genetics. Part A|October 15, 2011
Tissue-specific mosaicism for tetrasomy 9p uncovered by array CGHMarwa I Shehab, Inas Mazen, Susan Bint
Journal of Visualized Experiments : Jove|March 6, 2015
Array comparative genomic hybridization (array CGH) for detection of genomic copy number variantsJoo Wook Ahn, Michael Coldwell, Susan Bint, et al.
American Journal of Medical Genetics. Part A|April 6, 2006
Multicolor banding detects a complex three chromosome, seven breakpoint unbalanced rearrangement in an ICSI-derived fetus with multiple abnormalitiesMary J Seller, Susan Bint, Fred Kavalier, et al.
European Journal of Human Genetics : EJHG|September 27, 2003
Class II neocentromeres: a putative common neocentromere site in band 4q21.2Pamela C Warburton, Julian Barwell, Miranda Splitt, et al.
Molecular Cytogenetics|April 9, 2013
Array CGH as a first line diagnostic test in place of karyotyping for postnatal referrals - results from four years' clinical application for over 8,700 patientsJoo Wook Ahn, Susan Bint, Anne Bergbaum, et al.
European Journal of Medical Genetics|August 5, 2008
M-banding characterization of a 16p11.2p13.1 tandem duplication in a child with autism, neurodevelopmental delay and dysmorphismFarkhondeh Behjati, Yousef Shafaghati, Saghar Ghasemi Firouzabadi, et al.
Peerj|May 6, 2014
A new direction for prenatal chromosome microarray testing: software-targeting for detection of clinically significant chromosome imbalance without equivocal findingsJoo Wook Ahn, Susan Bint, Melita D Irving, et al.
Prenatal Diagnosis|December 13, 2024
Advances and Challenges in Prenatal Detection and Genetic Diagnosis of Upper Limb Anomalies: Analysis of a South London and Kent CohortFederica Ruscitti, Tara Giacchino, Lemonia Koutoulas, et al.
Hormone Research in Paediatrics|November 4, 2019
Xq27.1 Duplication Encompassing SOX3: Variable Phenotype and Smallest Duplication Associated with Hypopituitarism to Date - A Large Case Series of Unrelated Patients and a Literature ReviewVed Bhushan Arya, Garima Chawla, Aparna K R Nambisan, et al.
European Journal of Endocrinology|October 15, 2020
Rare CNVs provide novel insights into the molecular basis of GH and IGF-1 insensitivityEmily Cottrell, Claudia P Cabrera, Miho Ishida, et al.
Pageof 1