Y. Nomura

A new compound heterozygous mutation (W17X, 436 + 5G --> T) in the cytochrome P450c17 gene causes 17 alpha-hydroxylase/17,20-lyase deficiency.

A. Morikawa, T. Nagashima, K. Nagashima, 1998, The Journal of clinical endocrinology and metabolism.

Detection of skewed X-inactivation in two female carriers of vasopressin type 2 receptor gene mutation.

A. Morikawa, H. Mochizuki, T. Nagashima, 1997, The Journal of clinical endocrinology and metabolism.

Anterior Pituitary Dysfunction in Children with Idiopathic Central Diabetes Insipidus

A. Morikawa, T. Nagashima, K. Onigata, 1995 .

A Child with Necrotizing Infundibulo-Hypophysitis?

T. Nagashima, K. Onigata, K. Nagashima, 1994 .

A novel point mutation of thyroid hormone receptor beta gene in a family with resistance to thyroid hormone.

R. Weiss, S. Refetoff, R. Couch, 1997, Thyroid : official journal of the American Thyroid Association.

A sex reversal infant with XX karyotype and complete male external genitalia

T. Nagashima, K. Nagashima, H. Yagi, 1995, Acta paediatrica Japonica : Overseas edition.

A Novel Mutation of the Androgen Receptor Gene Ligand-Binding Domain (V734P) Associated with the Complete Androgen Insensitivity Syndrome

A. Morikawa, T. Nagashima, K. Onigata, 1995 .

A novel point mutation (R243Q) in exon 7 of the c-erbA beta thyroid hormone receptor gene in a family with resistance to thyroid hormone.

K. Hashizume, A. Morikawa, T. Nagashima, 1995, Thyroid.