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Melanie Babcock

Showing results (1-10 of 21) with videos related to

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Journal of Pediatric Genetics|September 15, 2016
Interstitial duplication of 22q13.2 in a girl with short stature, impaired speech and language, and dysmorphismJoy Samanich, Cristina Montagna, Bernice E Morrow, et al.
Genome Research|February 8, 2007
AT-rich repeats associated with chromosome 22q11.2 rearrangement disorders shape human genome architecture on Yq12Melanie Babcock, Svetlana Yatsenko, Pawel Stankiewicz, et al.
American Journal of Medical Genetics. Part A|February 4, 2012
Dextrocardia, atrial septal defect, severe developmental delay, facial anomalies, and supernumerary ribs in a child with a complex unbalanced 8;22 translocation including partial 8p duplicationKathleen Pope, Joy Samanich, K H Ramesh, et al.
International Journal of Pediatric Otorhinolaryngology|June 15, 2010
Mutational analysis of HOXA2 and SIX2 in a Bronx population with isolated microtiaDennis C Monks, Arthee Jahangir, Alan L Shanske, et al.
American Journal of Medical Genetics. Part A|March 19, 2011
Molecular characterization of an interstitial deletion of 1p31.3 in a patient with obesity and psychiatric illness and a review of the literatureMarilena Petti, Joy Samanich, Qiulu Pan, et al.
Genome Research|December 6, 2003
Shuffling of genes within low-copy repeats on 22q11 (LCR22) by Alu-mediated recombination events during evolutionMelanie Babcock, Adam Pavlicek, Elizabeth Spiteri, et al.
International Journal of Pediatric Otorhinolaryngology|April 13, 2010
GJB2 mutation spectrum in 209 hearing impaired individuals of predominantly Caribbean Hispanic and African descentJidong Shan, Janie Chobot-Rodd, Raquel Castellanos, et al.
Psychiatric Genetics|July 15, 2022
Chromosome 2q12.3-q13 copy number variants in patients with neurodevelopmental disorders: genotype-phenotype correlation and new hotspotsMahmoud Aarabi, Jacqueline Baumann, Melanie Babcock, et al.
The Journal of Applied Laboratory Medicine|January 3, 2024
Clinical Cytogenetics: Current Practices and BeyondMariam T Mathew, Melanie Babcock, Ying-Chen Claire Hou, et al.
American Journal of Medical Genetics. Part A|March 8, 2026
Unusual Recombinant Chromosome 6 Derived From a Parental Rearrangement With Complex Paracentric InversionsMelanie Babcock, Marwa Daghsni, Jessica Sebastian, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Journal of Pediatric Genetics|September 15, 2016
Interstitial duplication of 22q13.2 in a girl with short stature, impaired speech and language, and dysmorphismJoy Samanich, Cristina Montagna, Bernice E Morrow, et al.
Genome Research|February 8, 2007
AT-rich repeats associated with chromosome 22q11.2 rearrangement disorders shape human genome architecture on Yq12Melanie Babcock, Svetlana Yatsenko, Pawel Stankiewicz, et al.
American Journal of Medical Genetics. Part A|February 4, 2012
Dextrocardia, atrial septal defect, severe developmental delay, facial anomalies, and supernumerary ribs in a child with a complex unbalanced 8;22 translocation including partial 8p duplicationKathleen Pope, Joy Samanich, K H Ramesh, et al.
International Journal of Pediatric Otorhinolaryngology|June 15, 2010
Mutational analysis of HOXA2 and SIX2 in a Bronx population with isolated microtiaDennis C Monks, Arthee Jahangir, Alan L Shanske, et al.
American Journal of Medical Genetics. Part A|March 19, 2011
Molecular characterization of an interstitial deletion of 1p31.3 in a patient with obesity and psychiatric illness and a review of the literatureMarilena Petti, Joy Samanich, Qiulu Pan, et al.
Genome Research|December 6, 2003
Shuffling of genes within low-copy repeats on 22q11 (LCR22) by Alu-mediated recombination events during evolutionMelanie Babcock, Adam Pavlicek, Elizabeth Spiteri, et al.
International Journal of Pediatric Otorhinolaryngology|April 13, 2010
GJB2 mutation spectrum in 209 hearing impaired individuals of predominantly Caribbean Hispanic and African descentJidong Shan, Janie Chobot-Rodd, Raquel Castellanos, et al.
Psychiatric Genetics|July 15, 2022
Chromosome 2q12.3-q13 copy number variants in patients with neurodevelopmental disorders: genotype-phenotype correlation and new hotspotsMahmoud Aarabi, Jacqueline Baumann, Melanie Babcock, et al.
The Journal of Applied Laboratory Medicine|January 3, 2024
Clinical Cytogenetics: Current Practices and BeyondMariam T Mathew, Melanie Babcock, Ying-Chen Claire Hou, et al.
American Journal of Medical Genetics. Part A|March 8, 2026
Unusual Recombinant Chromosome 6 Derived From a Parental Rearrangement With Complex Paracentric InversionsMelanie Babcock, Marwa Daghsni, Jessica Sebastian, et al.
Pageof 3