E-LIB Suche - Ergebnisse für: Sakazume, Satoru

1

Interstitial microdeletions of 3q26.2q26.31 in two patients..:

Tamura, Takeaki ; Yamamoto Shimojima, Keiko ; Shiihara, Takashi...
American Journal of Medical Genetics Part A. 191 (2022) 2 - p. 400-407 , 2022

Link: https://doi.org/10.1002/..

2

Correction to: Growth references for Japanese individuals w..:

Isojima, Tsuyoshi ; Sakazume, Satoru ; Hasegawa, Tomonobu...
Pediatric Research. 92 (2022) 6 - p. 1820-1820 , 2022

Link: https://doi.org/10.1038/..

3

Acute lymphoblastic leukemia in a male with Simpson–Golabi–..:

Minatogawa, Mari ; Iwasaki, Fuminori ; Yokoi, Takayuki...
American Journal of Medical Genetics Part A. 176 (2018) 7 - p. 1680-1682 , 2018

Link: https://doi.org/10.1002/..

4

Validation of auxological reference values for Japanese chi..:

Isojima, Tsuyoshi ; Sakazume, Satoru ; Hasegawa, Tomonobu...
Clinical Pediatric Endocrinology. 26 (2017) 3 - p. 153-164 , 2017

Link: https://doi.org/10.1297/..

5

Holoprosencephaly with cerebellar vermis hypoplasia in 13q ..:

Mimaki, Masakazu ; Shiihara, Takashi ; Watanabe, Mio...
Brain and Development. 37 (2015) 7 - p. 714-718 , 2015

Link: https://doi.org/10.1016/..

6

Additional patients with 4q deletion: Severe growth delay a..:

Sakazume, Satoru ; Kido, Yasuhiro ; Murakami, Nobuyuki..
Pediatrics International. 57 (2015) 5 - p. 880-883 , 2015

Link: https://doi.org/10.1111/..

7

Breakpoint analysis of the recurrent constitutional t(8;22)..:

Mishra, Divya ; Kato, Takema ; Inagaki, Hidehito...
Molecular Cytogenetics. 7 (2014) 1 - p. , 2014

Link: https://doi.org/10.1186/..

8

Selection of infants who potentially have congenital anomal..:

Yoshino, Atsunori ; Honda, Masataka ; Sasaki, Naomi...
Clinical and Experimental Nephrology. 19 (2014) 4 - p. 678-682 , 2014

Link: https://doi.org/10.1007/..

9

Testosterone replacement therapy to improve secondary sexua..:

Kido, Yasuhiro ; Sakazume, Satoru ; Abe, Yoshiko...
American Journal of Medical Genetics Part A. 161 (2013) 9 - p. 2167-2173 , 2013

Link: https://doi.org/10.1002/..

10

Clinical correlations of mutations affecting six components..:

Kosho, Tomoki ; Okamoto, Nobuhiko ; Ohashi, Hirofumi...
American Journal of Medical Genetics Part A. 161 (2013) 6 - p. 1221-1237 , 2013

Link: https://doi.org/10.1002/..

11

Further characterization of atypical features in auriculoco..:

Kido, Yasuhiro ; Gordon, Christopher T. ; Sakazume, Satoru...
American Journal of Medical Genetics Part A. 161 (2013) 9 - p. 2339-2346 , 2013

Link: https://doi.org/10.1002/..

12

Growth hormone secretion and its effect on height in pediat..:

Oto, Yuji ; Obata, Kazuo ; Matsubara, Keiko...
American Journal of Medical Genetics Part A. 158A (2012) 6 - p. 1477-1480 , 2012

Link: https://doi.org/10.1002/..

13

Mutations affecting components of the SWI/SNF complex cause..:

Tsurusaki, Yoshinori ; Okamoto, Nobuhiko ; Ohashi, Hirofumi...
Nature Genetics. 44 (2012) 4 - p. 376-378 , 2012

Link: https://doi.org/10.1038/..

14

A founder mutation of CANT1 common in Korean and Japanese D..:

Dai, Jin ; Kim, Ok-Hwa ; Cho, Tae-Joon...
Journal of Human Genetics. 56 (2011) 5 - p. 398-400 , 2011

Link: https://doi.org/10.1038/..

15

Spread of X-chromosome inactivation into chromosome 15 is a..:

Sakazume, Satoru ; Ohashi, Hirofumi ; Sasaki, Yuki...
Human Genetics. 131 (2011) 1 - p. 121-130 , 2011

Link: https://doi.org/10.1007/..