Y. Shimakura

Isosexual Precocious Puberty and Polycystic Ovary Syndrome

N. Mesaki, T. Kamoda, H. Takita, 1996 .

Frequent occurrence of hypoalphalipoproteinemia due to mutant apolipoprotein A-I gene in the population: a population-based survey.

T. Arinami, H. Hamaguchi, C. Hirano, 1999, Human molecular genetics.

Comparison of basophil histamine release, eosinophil cationic protein and non‐specific airway responsiveness between mite‐sensitive asthmatic and non‐asthmatic children and non‐allergic controls

H. Takita, K. Takeda, Y. Shimakura, 1996, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

Family studies of the LDL receptor gene of relatively severe hereditary hypercholesterolemia associated with Achilles tendon xanthomas

K. Yamakawa, J. Sasaki, K. Arakawa, 1991, Human Genetics.

A novel complex mutation in the LDL receptor gene probably caused by the simultaneous occurrence of deletion and insertion in the same region

Tsutomu Kobayashi, H. Hamaguchi, H. Yanagi, 1994, Human Genetics.

Genetic Risk Factors for Coronary Heart Disease in the Japanese Population

T. Arinami, Tsuyoshi Tanaka, H. Hamaguchi, 1991 .

Failure to find evidence for association between voltage-gated sodium channel gene SCN2A variants and febrile seizures in humans

T. Arinami, E. Noguchi, N. Iwasaki, 2002, Neuroscience Letters.

Autosomal dominant hypoalphalipoproteinemia due to a completely defective apolipoprotein A-I gene.

T. Arinami, H. Hamaguchi, H. Yanagi, 1993, Biochemical and biophysical research communications.

Association of hypercholesterolemia and apolipoprotein E4 in school children

H. Hamaguchi, H. Yanagi, S. Tsuchiya, 1990, Clinical genetics.

Abnormal myelination in a patient with ring chromosome 18.

T. Arinami, N. Iwasaki, H. Hamaguchi, 1997, Neuropediatrics.

Ring chromosome 10 syndrome: case report and the possibility of clinical diagnosis

I. Kondo, M. Kaneko, T. Hirano, 1984, Clinical genetics.