G. Feldman

发表

Utility of the Pediatric Symptom Checklist as a psychosocial screen to meet the federal Early and Periodic Screening, Diagnosis, and Treatment (EPSDT) standards: a pilot study.

D. Kingdon, J. Murphy, M. Jellinek, 1996, The Journal of pediatrics.

Nodular glomerulopathy associated with nonamyloidotic kappa light chain deposits and excess immunoglobulin light chain synthesis.

L. Katz, J. Buxbaum, Feldman, 1980, The American journal of pathology.

Costello syndrome: phenotype, natural history, differential diagnosis, and possible cause.

J. Carey, M. Golabi, M. Norton, 1998, The Journal of pediatrics.

The campomelic syndrome in a singleton and monozygotic twins

B. Crandall, R. Sparkes, G. Austin, 1980, Clinical genetics.

Multiple carboxylase deficiency: clinical and biochemical improvement following neonatal biotin treatment.

D. Crowell, W. Nyhan, B. Wolf, 1981, Pediatrics.

Prenatal diagnosis of pyruvate carboxylase deficiency.

B. Wolf, C. Marsac, R. Berger, 1982, Clinica chimica acta; international journal of clinical chemistry.

The dup(17p) syndrome

R. Sparkes, G. Feldman, J. Baumer, 1982 .

Brief clinical report: the dup(17p) syndrome.

R. Sparkes, G. Feldman, J. Baumer, 1982, American journal of medical genetics.

Trisomy 17p associated with Charcot‐Marie‐Tooth neuropathy type 1A phenotype

T. Bird, N. Matsunami, A. Brothman, 1992, Neurology.

Infantile-onset multisystem inflammatory disease: a differential diagnosis of systemic juvenile rheumatoid arthritis.

J. Goldberg, D. Liberatore, C. D. De Cunto, 1997, The Journal of pediatrics.

The problem of partial trisomy 22 reconsidered

R. Sparkes, G. Feldman, 1978, Human Genetics.