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American Journal of Medical Genetics. Part A
|
August 14, 2012
Assessment of bone mineral status in children with Marfan syndrome
Monica Grover, Nicola Brunetti-Pierri, John Belmont, et al.
Human Mutation
|
June 21, 2012
The KAT6B-related disorders genitopatellar syndrome and Ohdo/SBBYS syndrome have distinct clinical features reflecting distinct molecular mechanisms
Philippe M Campeau, James T Lu, Brian C Dawson, et al.
Scientific Reports
|
December 8, 2017
mTORC1 Signaling is a Critical Regulator of Postnatal Tendon Development
Joohyun Lim, Elda Munivez, Ming-Ming Jiang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 28, 2020
Exome sequencing compared with standard genetic tests for critically ill infants with suspected genetic conditions
Hadley Stevens Smith, John M Swint, Seema R Lalani, et al.
Molecular Genetics and Metabolism Reports
|
July 15, 2014
Diagnosis of ALG12-CDG by exome sequencing in a case of severe skeletal dysplasia
Chaya Murali, James T Lu, Mahim Jain, et al.
American Journal of Medical Genetics. Part A
|
September 25, 2018
Heterozygous WNT1 variant causing a variable bone phenotype
Shatha Alhamdi, Yi-Chien Lee, Shimul Chowdhury, et al.
Human Molecular Genetics
|
April 14, 2012
miRNA-34c regulates Notch signaling during bone development
Yangjin Bae, Tao Yang, Huan-Chang Zeng, et al.
Nature Communications
|
April 12, 2017
MicroRNA miR-23a cluster promotes osteocyte differentiation by regulating TGF-β signalling in osteoblasts
Huan-Chang Zeng, Yangjin Bae, Brian C Dawson, et al.
Regenerative Medicine
|
August 23, 2021
Novel assessment of leukocyte-rich platelet-rich plasma on functional and patient-reported outcomes in knee osteoarthritis: a pilot study
Prathap Jayaram, Gu Eon Kang, Brett L Heldt, et al.
Journal of Human Genetics
|
December 23, 2016
Kaufman oculo-cerebro-facial syndrome in a child with small and absent terminal phalanges and absent nails
Ariana Kariminejad, Norbert Fonya Ajeawung, Bita Bozorgmehr, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 81) with videos related to
Sort By:
Page
of 9
American Journal of Medical Genetics. Part A
|
August 14, 2012
Assessment of bone mineral status in children with Marfan syndrome
Monica Grover, Nicola Brunetti-Pierri, John Belmont, et al.
Human Mutation
|
June 21, 2012
The KAT6B-related disorders genitopatellar syndrome and Ohdo/SBBYS syndrome have distinct clinical features reflecting distinct molecular mechanisms
Philippe M Campeau, James T Lu, Brian C Dawson, et al.
Scientific Reports
|
December 8, 2017
mTORC1 Signaling is a Critical Regulator of Postnatal Tendon Development
Joohyun Lim, Elda Munivez, Ming-Ming Jiang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 28, 2020
Exome sequencing compared with standard genetic tests for critically ill infants with suspected genetic conditions
Hadley Stevens Smith, John M Swint, Seema R Lalani, et al.
Molecular Genetics and Metabolism Reports
|
July 15, 2014
Diagnosis of ALG12-CDG by exome sequencing in a case of severe skeletal dysplasia
Chaya Murali, James T Lu, Mahim Jain, et al.
American Journal of Medical Genetics. Part A
|
September 25, 2018
Heterozygous WNT1 variant causing a variable bone phenotype
Shatha Alhamdi, Yi-Chien Lee, Shimul Chowdhury, et al.
Human Molecular Genetics
|
April 14, 2012
miRNA-34c regulates Notch signaling during bone development
Yangjin Bae, Tao Yang, Huan-Chang Zeng, et al.
Nature Communications
|
April 12, 2017
MicroRNA miR-23a cluster promotes osteocyte differentiation by regulating TGF-β signalling in osteoblasts
Huan-Chang Zeng, Yangjin Bae, Brian C Dawson, et al.
Regenerative Medicine
|
August 23, 2021
Novel assessment of leukocyte-rich platelet-rich plasma on functional and patient-reported outcomes in knee osteoarthritis: a pilot study
Prathap Jayaram, Gu Eon Kang, Brett L Heldt, et al.
Journal of Human Genetics
|
December 23, 2016
Kaufman oculo-cerebro-facial syndrome in a child with small and absent terminal phalanges and absent nails
Ariana Kariminejad, Norbert Fonya Ajeawung, Bita Bozorgmehr, et al.
Page
of 9