K. Hayashi

发表

Determination of HLA‐A, ‐C, ‐B, ‐DRB1 allele and haplotype frequency in Japanese population based on family study

D. Middleton, H. Saji, T. Futagami, 2015, Tissue antigens.

The rate of sister chromatid exchanges parallel to spontaneous chromosome breakage in Fanconi's anemia and to trenimon-induced aberrations in human lymphocytes and fibroblasts

W. Schmid, K. Hayashi, 1975, Humangenetik.

Further delineation of the clinical picture of trisomy for the distal segment of chromosome 13

A. Schinzel, W. Schmid, K. Hayashi, 1976, Human Genetics.

Mosaic-trisomy and pericentric inversion of chromosome 9 in a malformed boy

A. Schinzel, W. Schmid, K. Hayashi, 2004, Humangenetik.

Trisomy 9p due to paternal translocation, t(9;13)(q13;q12)

A. Schinzel, W. Schmid, K. Hayashi, 1975, Humangenetik.

Structural aberrations of chromosome 18

A. Schinzel, W. Schmid, K. Hayashi, 1975, Humangenetik.

Tandem duplication q14 and dicentric formation by end-to-end chromosome fusions in ataxia telangiectasia (AT)

W. Schmid, K. Hayashi, 1975, Humangenetik.

Tandem duplication q14 and dicentric formation by end-to-end chromosome fusions in ataxia telandiectasia (AT). Clinical and cytogenetic findings in 5 patients.

W. Schmid, K. Hayashi, 1975, Humangenetik.

Trisomy 8 mosaicism syndrome.

A. Schinzel, W. Schmid, K. Hayashi, 1974, Helvetica paediatrica acta.

Acute myeloid leukemia with t(6;9)(p23;q34)

Kosaka, Hiroki, Hasegawa, 2020, Definitions.