I. Porter

发表

D. Janerich, I. Porter, V. Logrillo, 1971, American journal of public health.

Ethical issues with genetic testing in pediatrics.

B. Wilfond, J. Botkin, M. Fallat, 2013, Pediatrics.

Long-term survival after bone marrow transplantation: a 15-year follow-up report of a patient with Wiskott-Aldrich syndrome.

F. Bach, M. Bortin, H. Meuwissen, 1984, The Journal of pediatrics.

American Academy of Pediatrics Committee on Bioethics: Infants with anencephaly as organ sources: ethical considerations.

E. Clayton, R. Dresser, E. Gates, 1992, Pediatrics.

Guidelines on Forgoing Life-Sustaining Medical Treatment

E. Clayton, R. Dresser, E. Gates, 2013, Pediatric Clinical Practice Guidelines & Policies.

Population and biological aspects of human mutation

I. Porter, E. Hook, 1981 .

Decreased HLA heterogeneity in parents of children with Down syndrome.

E. Hook, I. Porter, A. Willey, 1983, American journal of human genetics.

Electrophoretic heterogeneity of glucose-6-phosphate dehydrogenase and its relationship to enzyme deficiency in man.

S. Boyer, I. Porter, R. Weilbacher, 1962, Proceedings of the National Academy of Sciences of the United States of America.

Recent advances in molecular pathology: a review. Some aspects of chromosome changes in cancer.

W. Benedict, C. Brown, I. Porter, 1969, Experimental and molecular pathology.

VARIATION OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE IN DIFFERENT POPULATIONS.

S. Boyer, I. Porter, 1964, Lancet.

Chromosomal aberrations in an ovarian cystadenoma.

I. Porter, C. Brown, W. Benedict, 1969, Lancet.

Cytogenetic diagnosis of malignancy in recurrent meningioma.

I. Porter, R. Florentin, C. Brown, 1970, Lancet.

Chromosomes in malignancy.

I. Porter, C. Brown, W. Benedict, 1968, Lancet.

Age trends in the prevalence of the sickle cell trait.

S. Selvin, R. Herdman, D. Janerich, 1973, Health services reports.

Genetical linkage between the loci for glucose‐6‐phosphate dehydrogenase deficiency and colour‐blindness in American Negroes

V. McKusick, I. Porter, J. Schulze, 1962, Annals of human genetics.

Religious Objections to Medical Care

N. King, F. Vizcarrondo, R. Nelson, 1997, Pediatric Clinical Practice Guidelines & Policies.

THOMAS BARTHOLIN (1616–80) AND NIELS STEENSEN(1638–86) MASTER AND PUPIL

I. Porter, 1963, Medical History.

Ethics and the care of critically ill infants and children. American Academy of Pediatrics Committee on Bioethics.

F. Vizcarrondo, R. Nelson, Kathryn L. Moseley, 1996, Pediatrics.

GENETIC BASIS OF DRUG METABOLISM IN MAN.

I. Porter, 1964, Toxicology and applied pharmacology.

Variants of glucose 6-phosphate dehydrogenase.

I. Porter, 1968, Annals of internal medicine.

Myotonia, shortness of stature, and hip dysplasia. Schwartz-Jampel syndrome.

I. Porter, G. Hug, T. Mereu, 1969, American journal of diseases of children.

Indications for chromosome studies in clinical practice.

I. Porter, D. S. Kim, 1973, Pediatric annals.

Polyneuritis and central hypertension due to non-parotitic mumps.

C. Pallis, I. Porter, 1960, Lancet.

The cytogenetic diagnosis of malignancy in effusions.

I. Porter, W. Benedict, 1972, Acta cytologica.

CHROMOSOMES IN EFFUSIONS

I. Porter, W. Benedict, CharlesD. Brown, 1967 .

Studies of gastrointestinal bleeding caused by corticosteroids, salicylates, and other analgesics.

S. Lewis, J. Scott, A. Dixon, 1961, The Quarterly journal of medicine.

Human embryonic and fetal death

I. Porter, E. Hook, 1980 .

Research into the origin and treatment of muscular dystrophy. Proceedings of a workshop held at „De Hooge Vuursche”︁, Baarn, Holland. L.P. ten Kate, P.L. Pearson, and A.M. Stadhouders, editors. Current Clinical Practice Series 20. Excerpta Medica: Amsterdam, 1984

M. Baraitser, I. Porter, 1986 .

Control of hereditary disorders.

I. Porter, I H Porter, 1982, Annual review of public health.

Clinical aspects of congenital heart disease in mongolism.

R. Shaher, I. Porter, M. Bishop, 1972, The American journal of cardiology.

Paternal transmission of a D/G translocation of Down's syndrome.

I. Porter, C. Brown, D. Mele, 1966, American journal of diseases of children.

Double autosomal trisomy (trisomy D+G) with mosaicism.

I. Porter, C. Brown, W. Petersen, 1969, Journal of medical genetics.

The molecular basis of blood diseases. G. Stamatoyannopoulos, A.W. Nienhuis, P. Leder, P.W. Majerus. Philadelphia: W.B. Saunders Company, 1987, 747 pp $95.00

E. Beutler, I. Porter, 1988 .

Familial simple ectopia lentis: a case study.

J. Simon, S. Lichtenstein, I. Porter, 1985, Journal of pediatric ophthalmology and strabismus.

Linkage between Glucose-6-Phosphate Dehydrogenase Deficiency and Colour-Blindness

I. Porter, J. Schulze, V. A. McKusick, 1962, Nature.

SCREENING FOR ADA DEFICIENCY

H. Meuwissen, I. Porter, E. Moore, 1974, Pediatric Research.

Congenital defects: new directions in research

D. Janerich, R. Skalko, I. Porter, 1974 .

Population cytogenetics : studies in humans : proceedings of a Symposium on Human Population Cytogenetics sponsored by the Birth Defects Institute of the New York State Department of Health, held in Albany, New York, October 14-15, 1975

I. Porter, E. Hook, 1977 .

Alpha-fetoprotein and congenital disorders

G. Mizejewski, I. Porter, 1985 .

Medical genetics 1959

E. J. Battersby, N. Borhani, A. Lilienfeld, 1960 .

Long acrocentric marker chromosomes in malignant effusions and solid tumors.

I. Porter, C. Brown, W. Benedict, 1971, New York state journal of medicine.

THE NINETEENTH-CENTURY PHYSICIAN AND CARDIOLOGIST THOMAS BEVILL PEACOCK (1812–82)

I. Porter, 1962, Medical History.

SUCCESSFUL MARROW RE-TRANSPLANTATION FOLLOWING FAILURE OF FIRST TRANSPLANT FOR APLASTIC ANEMIA

H. Strauss, H. Meuwissen, I. Porter, 1974, Pediatric Research.