H. Madokoro

发表

Incidence of Minor Physical Anomalies in Patients With Early Infantile Autism

S. Ohdo, T. Sonoda, K. Hayakawa, 1986 .

Genetic Study on the Etiology of Congenital Heart Diseases

S. Ohdo, T. Nishiguchi, T. Sonoda, 1985 .

Partial trisomy for 19q due to paternal 17/19 reciprocal translocation

S. Ohdo, K. Kawaguchi, T. Sonoda, 1988, Japanese Journal of Human Genetics.

Kabuki make-up syndrome (Niikawa-Kuroki syndrome) associated with congenital heart disease.

S. Ohdo, T. Nishiguchi, K. Kawaguchi, 1985, Journal of medical genetics.

Sibs lacking characteristic features of duplication of distal 17q.

S. Ohdo, T. Sonoda, K. Ohba, 1989, Journal of medical genetics.

Mental retardation associated with congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth.

S. Ohdo, T. Sonoda, K. Hayakawa, 1986, Journal of medical genetics.

Interstitial Deletion of the Long Arm of Chromosome 13 and Retinoblastoma

S. Ohdo, T. Sonoda, K. Hayakawa, 1984 .

Partial monosomy 5p and partial trisomy 5q due to paternal pericentric inversion 5(p15.1q35.1)

S. Ohdo, K. Kawaguchi, T. Sonoda, 1989, Japanese Journal of Human Genetics.

Genetic and Diagnostic Studies of Mental Retardation

K. Naritomi, S. Ohdo, T. Terawaki, 1984 .

Incidence and Etiology of Mental Retardation in Patients with Congenital Heart Disease

S. Ohdo, T. Nishiguchi, T. Sonoda, 1986 .

Association of tetra-amelia, ectodermal dysplasia, hypoplastic lacrimal ducts and sacs opening towards the exterior, peculiar face, and developmental retardation.

S. Ohdo, T. Sonoda, M. Takei, 1987, Journal of medical genetics.

Interstitial deletion of the long arm of chromosome 5: 46,XX,del(5)(q13q22).

S. Ohdo, K. Hayakawa, H. Madokoro, 1982, Journal of medical genetics.

A new recognisable syndrome in three sibs with congenital heart disease, round face with depressed nasal bridge, short stature, and developmental retardation.

S. Ohdo, T. Sonoda, K. Ohba, 1988, Journal of Medical Genetics.

Congenital Heart Disease in a Case with Fetal Alcohol Syndrome: Clinical And Postmortem Findings

S. Ohdo, E. Sennari, H. Madokoro, 1984 .

Partial Trisomy 18q Associated with Terminal Deletion of 5p: 46, XX, +der (5), t(5; 18) (p15.3; q12.2) pat.

S. Ohdo, T. Sonoda, H. Madokoro, 1985 .

Sibslacking characteristic features ofduplication ofdistal 17q

S. Ohdo, T. Sonoda, K. Ohba, 1989 .

Infantile Autism and the Fragile X Syndrome in Japanese Children

S. Ohdo, T. Sonoda, K. Hayakawa, 1989, Acta paediatrica Japonica : Overseas edition.

Partial trisomy for 7p due to maternal balanced translocation

S. Ohdo, T. Sonoda, K. Suzumori, 1983, Japanese Journal of Human Genetics.

Familial X;Y translocation in a malformed male infant and his mother

S. Ohdo, Kiyomi Yamada, K. Kawaguchi, 1988, Japanese Journal of Human Genetics.