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Nature Reviews. Genetics
|
October 19, 2007
From microscopes to microarrays: dissecting recurrent chromosomal rearrangements
Beverly S Emanuel, Sulagna C Saitta
Neoreviews
|
November 30, 2022
Evaluating Genetic Disorders in the Neonate: The Role of Exome Sequencing in the NICU
T Niroshi Senaratne, Sulagna C Saitta
Current Allergy and Asthma Reports
|
November 1, 2018
Immune and Genetic Features of the Chromosome 22q11.2 Deletion (DiGeorge Syndrome)
Caroline Y Kuo, Rebecca Signer, Sulagna C Saitta
Molecular Syndromology
|
June 22, 2018
Interstitial Chromosome 3p13p14 Deletions: An Update and Review
Catherine A Hajek, Jianling Ji, Sulagna C Saitta
Neuron
|
February 3, 2009
MAP'ing CNS development and cognition: an ERKsome process
Ivy S Samuels, Sulagna C Saitta, Gary E Landreth
Molecular Syndromology
|
May 20, 2016
Interstitial Chromosome 3p14.1 Deletion due to a Maternal Insertion: Phenotype and Association with Balanced Parental Rearrangement
Catherine Hajek, Jia-Chi Wang, Loretta W Mahon, et al.
American Journal of Obstetrics & Gynecology MFM
|
June 15, 2024
Fetal and neonatal outcomes after "atypical findings" on cell-free fetal DNA screening
Jenny Y Mei, Aparna Murali, Alexa Nitka, et al.
Cancer Genetics
|
February 27, 2019
Embryonal rhabdomyosarcoma in a patient with a germline CBL pathogenic variant
Jianling Ji, Fariba Navid, Mathew C Hiemenz, et al.
American Journal of Medical Genetics. Part A
|
June 17, 2008
Intracytoplasmic sperm injection (ICSI) with transmission of a ring(Y) chromosome and ovotesticular disorder of sex development in offspring
Nancy B Spinner, Sulagna C Saitta, Daniel P Delaney, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
July 4, 2008
Deletion of ERK2 mitogen-activated protein kinase identifies its key roles in cortical neurogenesis and cognitive function
Ivy S Samuels, J Colleen Karlo, Alicia N Faruzzi, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 30) with videos related to
Sort By:
Page
of 3
Nature Reviews. Genetics
|
October 19, 2007
From microscopes to microarrays: dissecting recurrent chromosomal rearrangements
Beverly S Emanuel, Sulagna C Saitta
Neoreviews
|
November 30, 2022
Evaluating Genetic Disorders in the Neonate: The Role of Exome Sequencing in the NICU
T Niroshi Senaratne, Sulagna C Saitta
Current Allergy and Asthma Reports
|
November 1, 2018
Immune and Genetic Features of the Chromosome 22q11.2 Deletion (DiGeorge Syndrome)
Caroline Y Kuo, Rebecca Signer, Sulagna C Saitta
Molecular Syndromology
|
June 22, 2018
Interstitial Chromosome 3p13p14 Deletions: An Update and Review
Catherine A Hajek, Jianling Ji, Sulagna C Saitta
Neuron
|
February 3, 2009
MAP'ing CNS development and cognition: an ERKsome process
Ivy S Samuels, Sulagna C Saitta, Gary E Landreth
Molecular Syndromology
|
May 20, 2016
Interstitial Chromosome 3p14.1 Deletion due to a Maternal Insertion: Phenotype and Association with Balanced Parental Rearrangement
Catherine Hajek, Jia-Chi Wang, Loretta W Mahon, et al.
American Journal of Obstetrics & Gynecology MFM
|
June 15, 2024
Fetal and neonatal outcomes after "atypical findings" on cell-free fetal DNA screening
Jenny Y Mei, Aparna Murali, Alexa Nitka, et al.
Cancer Genetics
|
February 27, 2019
Embryonal rhabdomyosarcoma in a patient with a germline CBL pathogenic variant
Jianling Ji, Fariba Navid, Mathew C Hiemenz, et al.
American Journal of Medical Genetics. Part A
|
June 17, 2008
Intracytoplasmic sperm injection (ICSI) with transmission of a ring(Y) chromosome and ovotesticular disorder of sex development in offspring
Nancy B Spinner, Sulagna C Saitta, Daniel P Delaney, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
July 4, 2008
Deletion of ERK2 mitogen-activated protein kinase identifies its key roles in cortical neurogenesis and cognitive function
Ivy S Samuels, J Colleen Karlo, Alicia N Faruzzi, et al.
Page
of 3