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American Journal of Medical Genetics. Part A
|
November 27, 2014
Expanding the clinical spectrum of ocular anomalies in Noonan syndrome: Axenfeld-anomaly in a child with PTPN11 mutation
Andrea Guerin, Joyce So, Kamiar Mireskandari, et al.
American Journal of Medical Genetics. Part A
|
October 6, 2017
Noncompaction cardiomyopathy in an infant with Walker-Warburg syndrome
Sarah Abdullah, Cynthia Hawkins, Gregory Wilson, et al.
Frontiers in Genetics
|
September 5, 2022
Prenatal phenotype analysis and mutation identification of a fetus with meckel gruber syndrome
Laura Moreno-Leon, Marco A Quezada-Ramirez, Evan Bilsbury, et al.
American Journal of Medical Genetics. Part A
|
September 27, 2022
Scope of coverage of medical genetics and genomics in pre-clerkship programs of Canadian faculties of medicine: A curriculum analysis
Jade Ouellet, Julie Lapointe, Camille Raîche, et al.
American Journal of Medical Genetics. Part A
|
November 12, 2020
Bilateral severe microphthalmia in a neonate with trisomy 8 mosaicism: A new finding
Bevan Sanderson, Courtney Leach, Mike Zein, et al.
American Journal of Medical Genetics. Part A
|
December 10, 2015
Triplication of 16p12.1p12.3 associated with developmental and growth delay and distinctive facial features
Graeme A M Nimmo, Andrea Guerin, Ramses Badilla-Porras, et al.
American Journal of Medical Genetics. Part A
|
March 22, 2022
Novel FGF9 variant contributes to multiple synostoses syndrome 3
Stephanie M Dobson, Courtney Kiss, Daniel Borschneck, et al.
Epidemiology (Cambridge, Mass.)
|
February 16, 2007
Trends in obesity in pregnancy
Joel G Ray, Rosane Nisenbaum, Gita Singh, et al.
American Journal of Medical Genetics. Part A
|
September 12, 2012
Interstitial deletion of 11q-implicating the KIRREL3 gene in the neurocognitive delay associated with Jacobsen syndrome
Andrea Guerin, Dimitri J Stavropoulos, Yaser Diab, et al.
Journal of Human Genetics
|
December 13, 2019
Exome sequencing identifies de novo splicing variant in XRCC6 in sporadic case of autism
Calvin P Sjaarda, Shalandra Wood, Amy J M McNaughton, et al.
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of 4
Search research articles
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Showing results (11-20 of 39) with videos related to
Sort By:
Page
of 4
American Journal of Medical Genetics. Part A
|
November 27, 2014
Expanding the clinical spectrum of ocular anomalies in Noonan syndrome: Axenfeld-anomaly in a child with PTPN11 mutation
Andrea Guerin, Joyce So, Kamiar Mireskandari, et al.
American Journal of Medical Genetics. Part A
|
October 6, 2017
Noncompaction cardiomyopathy in an infant with Walker-Warburg syndrome
Sarah Abdullah, Cynthia Hawkins, Gregory Wilson, et al.
Frontiers in Genetics
|
September 5, 2022
Prenatal phenotype analysis and mutation identification of a fetus with meckel gruber syndrome
Laura Moreno-Leon, Marco A Quezada-Ramirez, Evan Bilsbury, et al.
American Journal of Medical Genetics. Part A
|
September 27, 2022
Scope of coverage of medical genetics and genomics in pre-clerkship programs of Canadian faculties of medicine: A curriculum analysis
Jade Ouellet, Julie Lapointe, Camille Raîche, et al.
American Journal of Medical Genetics. Part A
|
November 12, 2020
Bilateral severe microphthalmia in a neonate with trisomy 8 mosaicism: A new finding
Bevan Sanderson, Courtney Leach, Mike Zein, et al.
American Journal of Medical Genetics. Part A
|
December 10, 2015
Triplication of 16p12.1p12.3 associated with developmental and growth delay and distinctive facial features
Graeme A M Nimmo, Andrea Guerin, Ramses Badilla-Porras, et al.
American Journal of Medical Genetics. Part A
|
March 22, 2022
Novel FGF9 variant contributes to multiple synostoses syndrome 3
Stephanie M Dobson, Courtney Kiss, Daniel Borschneck, et al.
Epidemiology (Cambridge, Mass.)
|
February 16, 2007
Trends in obesity in pregnancy
Joel G Ray, Rosane Nisenbaum, Gita Singh, et al.
American Journal of Medical Genetics. Part A
|
September 12, 2012
Interstitial deletion of 11q-implicating the KIRREL3 gene in the neurocognitive delay associated with Jacobsen syndrome
Andrea Guerin, Dimitri J Stavropoulos, Yaser Diab, et al.
Journal of Human Genetics
|
December 13, 2019
Exome sequencing identifies de novo splicing variant in XRCC6 in sporadic case of autism
Calvin P Sjaarda, Shalandra Wood, Amy J M McNaughton, et al.
Page
of 4