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Haploinsufficiency for SOX9, the master chondrogenesis transcription factor, can underlie campomelic...
Sox9 is a Sry-related HMG-domain containing transcription factor. Lines of evidence suggest that Sox...
Induction of testis development in mammals requires the presence of the Y-chromosome gene SPY. This ...
abstractpublished_or_final_versionOrthopaedics and TraumatologyDoctoralDoctor of Philosoph
An international course for phycisians and scientistsThe 4th Annual Introductory Course on Skeletal ...
Symposium in Honor of Patrick Tam FRS "60 Years & Still Gastrulating"Conference Theme: From Embryolo...
Campomelic dysplasia (CD) is a congenital disease causing skeletal defects, such as shortened and an...
Human SOX9 mutations cause the skeletal malformation syndrome campomelic dysplasia (CD). Complete in...
cause campomelic dysplasia, a severe skeletal dysmorphology syndrome in humans characterized by a g...
In eutherian mammals, the Y-chromosome gene SRY is required for induction of testis development. Alt...
The involvement of SOX9 in congenital skeletal malformation was demonstrated 15 years ago with the i...
Haploinsufficiency of SOX9, which encodes a homeodomain transcription factor, results in Campomelic ...
Two decades after the discovery that heterozygous mutations within and around SOX9 cause campomelic ...
It has previously been shown that, in the heterozygous state, mutations in the SOX9 gene cause campo...
AbstractThe transcription factor Sox9 was first discovered in patients with campomelic dysplasia, a ...
Haploinsufficiency for SOX9, the master chondrogenesis transcription factor, can underlie campomelic...
Sox9 is a Sry-related HMG-domain containing transcription factor. Lines of evidence suggest that Sox...
Induction of testis development in mammals requires the presence of the Y-chromosome gene SPY. This ...
abstractpublished_or_final_versionOrthopaedics and TraumatologyDoctoralDoctor of Philosoph
An international course for phycisians and scientistsThe 4th Annual Introductory Course on Skeletal ...
Symposium in Honor of Patrick Tam FRS "60 Years & Still Gastrulating"Conference Theme: From Embryolo...
Campomelic dysplasia (CD) is a congenital disease causing skeletal defects, such as shortened and an...
Human SOX9 mutations cause the skeletal malformation syndrome campomelic dysplasia (CD). Complete in...
cause campomelic dysplasia, a severe skeletal dysmorphology syndrome in humans characterized by a g...
In eutherian mammals, the Y-chromosome gene SRY is required for induction of testis development. Alt...
The involvement of SOX9 in congenital skeletal malformation was demonstrated 15 years ago with the i...
Haploinsufficiency of SOX9, which encodes a homeodomain transcription factor, results in Campomelic ...
Two decades after the discovery that heterozygous mutations within and around SOX9 cause campomelic ...
It has previously been shown that, in the heterozygous state, mutations in the SOX9 gene cause campo...
AbstractThe transcription factor Sox9 was first discovered in patients with campomelic dysplasia, a ...
Haploinsufficiency for SOX9, the master chondrogenesis transcription factor, can underlie campomelic...
Sox9 is a Sry-related HMG-domain containing transcription factor. Lines of evidence suggest that Sox...
Induction of testis development in mammals requires the presence of the Y-chromosome gene SPY. This ...