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American Journal of Medical Genetics
|
September 5, 2002
Apparently new osteodysplastic and primordial short stature with severe microdontia, opalescent teeth, and rootless molars in two siblings
Piranit N Kantaputra
American Journal of Medical Genetics. Part A
|
November 24, 2004
A newly recognized syndrome involving limbs, pelvis, and genital organs or a variant of Al-Awadi/Raas-Rothschild syndrome?
Piranit N Kantaputra, Pranoot Tanpaiboon
Clinical Genetics
|
August 14, 2018
Genetic regulatory pathways of split-hand/foot malformation
Piranit N Kantaputra, Bruce M Carlson
American Journal of Medical Genetics. Part A
|
November 9, 2011
Split hand-split foot-ectodermal dysplasia and amelogenesis imperfecta with a TP63 mutation
Piranit N Kantaputra, Oranart Matangkasombut, Warissara Sripathomsawat
American Journal of Medical Genetics. Part A
|
October 16, 2010
A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome
Piranit N Kantaputra, Stefan Mundlos, Warissara Sripathomsawat
American Journal of Medical Genetics. Part A
|
September 17, 2004
Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies: confirmation of a new syndrome
Piranit N Kantaputra, Pranoot Tanpaiboon, Kevalee Unachak, et al.
American Journal of Medical Genetics
|
March 29, 2002
Van der Woude syndrome with sensorineural hearing loss, large craniofacial sinuses, dental pulp stones, and minor limb anomalies: report of a four-generation Thai family
Piranit N Kantaputra, Yupa Sumitsawan, Brian C Schutte, et al.
American Journal of Medical Genetics. Part A
|
September 27, 2006
A newly recognized polyosteolysis/hyperostosis syndrome
Piranit N Kantaputra, Chanin Limwongse, Ajchara Koolvisoot, et al.
American Journal of Medical Genetics
|
September 5, 2002
A dominantly inherited malformation syndrome with short stature, upper limb anomaly, minor craniofacial anomalies, and absence of TBX5 mutations: report of a Thai family
Piranit N Kantaputra, Kentaro Yamasaki, Takafumi Ishida, et al.
American Journal of Medical Genetics
|
April 5, 2002
A Thai mother and son with distal symphalangism, hypoplastic carpal bones, microdontia, dental pulp stones, and narrowing of the zygomatic arch: a new distal symphalangism syndrome?
Piranit N Kantaputra, Akira Kinoshita, Chanin Limwonges, et al.
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Search research articles
Search
Showing results (1-10 of 22) with videos related to
Sort By:
Page
of 3
American Journal of Medical Genetics
|
September 5, 2002
Apparently new osteodysplastic and primordial short stature with severe microdontia, opalescent teeth, and rootless molars in two siblings
Piranit N Kantaputra
American Journal of Medical Genetics. Part A
|
November 24, 2004
A newly recognized syndrome involving limbs, pelvis, and genital organs or a variant of Al-Awadi/Raas-Rothschild syndrome?
Piranit N Kantaputra, Pranoot Tanpaiboon
Clinical Genetics
|
August 14, 2018
Genetic regulatory pathways of split-hand/foot malformation
Piranit N Kantaputra, Bruce M Carlson
American Journal of Medical Genetics. Part A
|
November 9, 2011
Split hand-split foot-ectodermal dysplasia and amelogenesis imperfecta with a TP63 mutation
Piranit N Kantaputra, Oranart Matangkasombut, Warissara Sripathomsawat
American Journal of Medical Genetics. Part A
|
October 16, 2010
A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome
Piranit N Kantaputra, Stefan Mundlos, Warissara Sripathomsawat
American Journal of Medical Genetics. Part A
|
September 17, 2004
Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies: confirmation of a new syndrome
Piranit N Kantaputra, Pranoot Tanpaiboon, Kevalee Unachak, et al.
American Journal of Medical Genetics
|
March 29, 2002
Van der Woude syndrome with sensorineural hearing loss, large craniofacial sinuses, dental pulp stones, and minor limb anomalies: report of a four-generation Thai family
Piranit N Kantaputra, Yupa Sumitsawan, Brian C Schutte, et al.
American Journal of Medical Genetics. Part A
|
September 27, 2006
A newly recognized polyosteolysis/hyperostosis syndrome
Piranit N Kantaputra, Chanin Limwongse, Ajchara Koolvisoot, et al.
American Journal of Medical Genetics
|
September 5, 2002
A dominantly inherited malformation syndrome with short stature, upper limb anomaly, minor craniofacial anomalies, and absence of TBX5 mutations: report of a Thai family
Piranit N Kantaputra, Kentaro Yamasaki, Takafumi Ishida, et al.
American Journal of Medical Genetics
|
April 5, 2002
A Thai mother and son with distal symphalangism, hypoplastic carpal bones, microdontia, dental pulp stones, and narrowing of the zygomatic arch: a new distal symphalangism syndrome?
Piranit N Kantaputra, Akira Kinoshita, Chanin Limwonges, et al.
Page
of 3