Norio Niikawa

Chromosome-band-specific painting: chromosome in situ suppression hybridization using PCR products from a microdissected chromosome band as a probe pool

Naoki Harada, Roeland W. Dirks, Koh-ichiro Yoshiura, 1992, Human Genetics.

Uniparental disomy and imprinting defects in Japanese patients with Angelman syndrome

Shinji Saitoh, Kyoko Takano, Akira Sudo, 2005, Brain and Development.

A SNP in the ABCC11 gene is the determinant of human earwax type

Yusuke Nakamura, Tadashi Kaname, Katsushi Tokunaga, 2006, Nature Genetics.

New from NPG

Tadashi Kaname, Kenji Naritomi, Hiroshi Doi, 2012, Nature Medicine.

Heterozygous TGFBR2 mutations in Marfan syndrome

Yusuke Nakamura, Naomichi Matsumoto, Mathilde Varret, 2004, Nature Genetics.

Identification of a 3.0-kb major recombination hotspot in patients with Sotos syndrome who carry a common 1.9-Mb microdeletion.

Naomichi Matsumoto, Naoki Harada, Tohru Ohta, 2005, American journal of human genetics.

Domain-specific mutations in TGFB1 result in Camurati-Engelmann disease

Naoyuki Taniguchi, Jeffrey C. Murray, Kunihiro Yoshida, 2000, Nature Genetics.

BAC array CGH reveals genomic aberrations in idiopathic mental retardation

Naomichi Matsumoto, Kenji Kurosawa, Yoshio Makita, 2006, American journal of medical genetics. Part A.

Fifty microdeletions among 112 cases of Sotos syndrome: Low copy repeats possibly mediate the common deletion

Jan-Fang Cheng, Naomichi Matsumoto, Kenji Kurosawa, 2003, Human mutation.