Noritaka Iwatani

Deletion of NKX2.1 gene encoding thyroid transcription factor-1 in two siblings with hypothyroidism and respiratory failure

Noritaka Iwatani, Hiroyo Mabe, K Devriendt et al. · The Journal of Pediatrics · 2000 · 169 citations

Nkx2.1 Gene, Genetics, Thyroid Disease +9

A new mutation causing inherited growth hormone deficiency: a compound heterozygote of a 6.7 kb deletion and a two base deletion in the third exon of the GH-1 gene

Yutaka Igarashi, Masamichi Ogawa, Takashi Kamijo et al. · Human Molecular Genetics · 1993 · 42 citations

Reproductive Sciences, Kb Deletion, Base Deletion +21

The majority of the marker chromosomes in Japanese patients with stigmata of turner syndrome are derived from Y chromosomes

Shigeo Nagafuchi, Takashi Tamura, Yutaka Nakahori et al. · Human Genetics · 1992 · 40 citations

Mendelian Disorder, Y Chromosomes, Cytogenetics +10

Effects of exogenous melatonin on pituitary hormones in humans

Tosirou Ninomiya, Noritaka Iwatani, Akemi Tomoda et al. · Clinical Physiology · 2001 · 27 citations

Treatment of pituitary dwarfism with methionyl human growth hormone in Japan.

Kazue Takano, KAZUO SHIZUME, Naomi Hizuka et al. · Endocrinologia Japonica · 1986 · 19 citations · Full text