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American Journal of Medical Genetics. Part A
|
January 6, 2005
Double-layered patella in multiple epiphyseal dysplasia is not exclusive to DTDST mutation
Eiji Nakashima, Shiro Ikegawa, Hirofumi Ohashi, et al.
American Journal of Medical Genetics. Part A
|
June 7, 2016
Distinctive skeletal phenotype in high bone mass osteogenesis imperfecta due to a COL1A2 cleavage site mutation
Gen Nishimura, Masahiro Nakajima, Kazuharu Takikawa, et al.
Human Genome Variation
|
June 9, 2016
A novel type II collagen gene mutation in a family with spondyloepiphyseal dysplasia and extensive intrafamilial phenotypic diversity
Yasuharu Nakashima, Yuma Sakamoto, Gen Nishimura, et al.
AJR. American Journal of Roentgenology
|
March 23, 2017
Follow-Up Study on Fetal CT Radiation Dose in Japan: Validating the Decrease in Radiation Dose
Osamu Miyazaki, Hideaki Sawai, Takahiro Yamada, et al.
Pediatric Radiology
|
April 4, 2015
Sclerosteosis (craniotubular hyperostosis-syndactyly) with complex hyperphalangy of the index finger
Hiroko Yagi, Masaki Takagi, Yukihiro Hasegawa, et al.
American Journal of Medical Genetics. Part A
|
February 25, 2003
Microcephalic osteodysplastic primordial short stature type II with cafe-au-lait spots and moyamoya disease
Gen Nishimura, Tomonobu Hasegawa, Motoko Fujino, et al.
Genes, Chromosomes & Cancer
|
January 25, 2002
Diaphyseal medullary stenosis with malignant fibrous histiocytoma: further evidence for loss of heterozygosity involving 9p21-22 in tumor tissue
Koji Muroya, Gen Nishimura, Hideo Douya, et al.
American Journal of Medical Genetics. Part A
|
April 1, 2006
Familial Klippel-Feil anomaly and t(5;8)(q35.1;p21.1) translocation
Masahiro Goto, Gen Nishimura, Toshiro Nagai, et al.
American Journal of Medical Genetics. Part A
|
July 12, 2005
Microdeletion in the SHOX 3' region associated with skeletal phenotypes of Langer mesomelic dysplasia in a 45,X/46,X,r(X) infant and Leri-Weill dyschondrosteosis in her 46,XX mother: implication for the SHOX enhancer
Maki Fukami, Torayuki Okuyama, Shunji Yamamori, et al.
Pediatric Radiology
|
April 17, 2014
Nationwide radiation dose survey of computed tomography for fetal skeletal dysplasias
Osamu Miyazaki, Hideaki Sawai, Jun Murotsuki, et al.
Page
of 34
Search research articles
Search
Showing results (31-40 of 334) with videos related to
Sort By:
Page
of 34
American Journal of Medical Genetics. Part A
|
January 6, 2005
Double-layered patella in multiple epiphyseal dysplasia is not exclusive to DTDST mutation
Eiji Nakashima, Shiro Ikegawa, Hirofumi Ohashi, et al.
American Journal of Medical Genetics. Part A
|
June 7, 2016
Distinctive skeletal phenotype in high bone mass osteogenesis imperfecta due to a COL1A2 cleavage site mutation
Gen Nishimura, Masahiro Nakajima, Kazuharu Takikawa, et al.
Human Genome Variation
|
June 9, 2016
A novel type II collagen gene mutation in a family with spondyloepiphyseal dysplasia and extensive intrafamilial phenotypic diversity
Yasuharu Nakashima, Yuma Sakamoto, Gen Nishimura, et al.
AJR. American Journal of Roentgenology
|
March 23, 2017
Follow-Up Study on Fetal CT Radiation Dose in Japan: Validating the Decrease in Radiation Dose
Osamu Miyazaki, Hideaki Sawai, Takahiro Yamada, et al.
Pediatric Radiology
|
April 4, 2015
Sclerosteosis (craniotubular hyperostosis-syndactyly) with complex hyperphalangy of the index finger
Hiroko Yagi, Masaki Takagi, Yukihiro Hasegawa, et al.
American Journal of Medical Genetics. Part A
|
February 25, 2003
Microcephalic osteodysplastic primordial short stature type II with cafe-au-lait spots and moyamoya disease
Gen Nishimura, Tomonobu Hasegawa, Motoko Fujino, et al.
Genes, Chromosomes & Cancer
|
January 25, 2002
Diaphyseal medullary stenosis with malignant fibrous histiocytoma: further evidence for loss of heterozygosity involving 9p21-22 in tumor tissue
Koji Muroya, Gen Nishimura, Hideo Douya, et al.
American Journal of Medical Genetics. Part A
|
April 1, 2006
Familial Klippel-Feil anomaly and t(5;8)(q35.1;p21.1) translocation
Masahiro Goto, Gen Nishimura, Toshiro Nagai, et al.
American Journal of Medical Genetics. Part A
|
July 12, 2005
Microdeletion in the SHOX 3' region associated with skeletal phenotypes of Langer mesomelic dysplasia in a 45,X/46,X,r(X) infant and Leri-Weill dyschondrosteosis in her 46,XX mother: implication for the SHOX enhancer
Maki Fukami, Torayuki Okuyama, Shunji Yamamori, et al.
Pediatric Radiology
|
April 17, 2014
Nationwide radiation dose survey of computed tomography for fetal skeletal dysplasias
Osamu Miyazaki, Hideaki Sawai, Jun Murotsuki, et al.
Page
of 34