Search research articles
Contact Us
Filters
Showing results (61-70 of 112) with videos related to
Page
of 12
Sort By:
American Journal of Medical Genetics. Part A
|
April 16, 2005
Congenital anomaly of cervical vertebrae is a major complication of Rubinstein-Taybi syndrome
Toshiyuki Yamamoto, Kenji Kurosawa, Mitsuo Masuno, et al.
American Journal of Medical Genetics. Part A
|
August 14, 2012
Expression analysis of a 17p terminal deletion, including YWHAE, but not PAFAH1B1, associated with normal brain structure on MRI in a young girl
Keisuke Enomoto, Yasuhiro Kishitani, Makiko Tominaga, et al.
Human Genome Variation
|
May 16, 2018
Novel <i>COL4A1</i> mutation in a fetus with early prenatal onset of schizencephaly
Yota Sato, Jun Shibasaki, Noriko Aida, et al.
Journal of Human Genetics
|
December 5, 2014
Mutations in the glutaminyl-tRNA synthetase gene cause early-onset epileptic encephalopathy
Hirofumi Kodera, Hitoshi Osaka, Mizue Iai, et al.
No to Hattatsu = Brain and Development
|
January 29, 2005
[A case of long-term survival of a patient with infantile Alexander disease diagnosed by DNA analysis]
Kazuyo Wakabayashi, Mizue Lai, Kaori Masuko, et al.
Molecular Genetics & Genomic Medicine
|
July 19, 2017
Haploinsufficiency of <i>BCL11A</i> associated with cerebellar abnormalities in 2p15p16.1 deletion syndrome
Hiroko Shimbo, Takayuki Yokoi, Noriko Aida, et al.
Magnetic Resonance in Medical Sciences : MRMS : an Official Journal of Japan Society of Magnetic Resonance in Medicine
|
September 29, 2009
Diffusion-weighted imaging of an atypical teratoid/rhabdoid tumor of the cervical spine
Tetsu Niwa, Noriko Aida, Mio Tanaka, et al.
Radiographics : a Review Publication of the Radiological Society of North America, Inc
|
January 17, 2013
Syndromes associated with vascular tumors and malformations: a pictorial review
Taiki Nozaki, Shunsuke Nosaka, Osamu Miyazaki, et al.
American Journal of Medical Genetics. Part A
|
June 11, 2015
Polyostotic osteolysis and hypophosphatemic rickets with elevated serum fibroblast growth factor 23: A case report
Takeshi Sato, Koji Muroya, Yumi Asakura, et al.
Pediatric Surgery International
|
June 29, 2004
Pericardial hemangioma presenting fetal cardiac tamponade and postnatal bronchostenosis
Norihiko Kitagawa, Youkatsu Ohhama, Yoshimitsu Fukuzato, et al.
Page
of 12
Search research articles
Search
Showing results (61-70 of 112) with videos related to
Sort By:
Page
of 12
American Journal of Medical Genetics. Part A
|
April 16, 2005
Congenital anomaly of cervical vertebrae is a major complication of Rubinstein-Taybi syndrome
Toshiyuki Yamamoto, Kenji Kurosawa, Mitsuo Masuno, et al.
American Journal of Medical Genetics. Part A
|
August 14, 2012
Expression analysis of a 17p terminal deletion, including YWHAE, but not PAFAH1B1, associated with normal brain structure on MRI in a young girl
Keisuke Enomoto, Yasuhiro Kishitani, Makiko Tominaga, et al.
Human Genome Variation
|
May 16, 2018
Novel <i>COL4A1</i> mutation in a fetus with early prenatal onset of schizencephaly
Yota Sato, Jun Shibasaki, Noriko Aida, et al.
Journal of Human Genetics
|
December 5, 2014
Mutations in the glutaminyl-tRNA synthetase gene cause early-onset epileptic encephalopathy
Hirofumi Kodera, Hitoshi Osaka, Mizue Iai, et al.
No to Hattatsu = Brain and Development
|
January 29, 2005
[A case of long-term survival of a patient with infantile Alexander disease diagnosed by DNA analysis]
Kazuyo Wakabayashi, Mizue Lai, Kaori Masuko, et al.
Molecular Genetics & Genomic Medicine
|
July 19, 2017
Haploinsufficiency of <i>BCL11A</i> associated with cerebellar abnormalities in 2p15p16.1 deletion syndrome
Hiroko Shimbo, Takayuki Yokoi, Noriko Aida, et al.
Magnetic Resonance in Medical Sciences : MRMS : an Official Journal of Japan Society of Magnetic Resonance in Medicine
|
September 29, 2009
Diffusion-weighted imaging of an atypical teratoid/rhabdoid tumor of the cervical spine
Tetsu Niwa, Noriko Aida, Mio Tanaka, et al.
Radiographics : a Review Publication of the Radiological Society of North America, Inc
|
January 17, 2013
Syndromes associated with vascular tumors and malformations: a pictorial review
Taiki Nozaki, Shunsuke Nosaka, Osamu Miyazaki, et al.
American Journal of Medical Genetics. Part A
|
June 11, 2015
Polyostotic osteolysis and hypophosphatemic rickets with elevated serum fibroblast growth factor 23: A case report
Takeshi Sato, Koji Muroya, Yumi Asakura, et al.
Pediatric Surgery International
|
June 29, 2004
Pericardial hemangioma presenting fetal cardiac tamponade and postnatal bronchostenosis
Norihiko Kitagawa, Youkatsu Ohhama, Yoshimitsu Fukuzato, et al.
Page
of 12