P. J. Waardenburg

发表

ON VARIOUS RECESSIVE BIOTYPES OF LEBER'S CONGENITAL AMAUROSIS *

J. Schappert-Kimmijser, P. J. Waardenburg, 1963, Acta ophthalmologica.

A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness.

P. J. Waardenburg, 1951, American journal of human genetics.

Butterfly-shaped pigment dystrophy of the fovea.

A. Deutman, H. Henkes, P. J. Waardenburg, 1970, Archives of ophthalmology.

A SPECIFIC TYPE OF DOMINANT PROGRESSIVE DYSTROPHY OF THE CORNEA, DEVELOPING AFTER BIRTH

P. J. Waardenburg, G. H. Jankers, 1961, Acta ophthalmologica.

Some notes on publications of Professor Arnold Sorsby and on Aland eye disease (Forsius-Eriksson syndrome).

P. J. Waardenburg, 1970, Journal of Medical Genetics.

X‐CHROMOSOMAL OCULAR ALBINISM IN A DUTCH FAMILY *

P. J. Waardenburg, J. Bosch, 1956, Annals of human genetics.

HYPERPLASIA INTEROCULARIS CUM DYSTOPIA LATEROVERSA CANTHI MEDIALIS, BLEPHAROPHIMOSIS, DYSCHROMIA IRIDOCUTANEA ET DYSPLASIA AUDITIVA

P. J. Waardenburg, 1957 .

ALBINOS WITH NORMAL OFFSPRING

P. J. Waardenburg, 1952, The British journal of ophthalmology.

Hypoplasia of the central fovea.

P. J. Waardenburg, 1948, Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde.

Twin research in ophthalmology

P. J. Waardenburg, 2004, Documenta Ophthalmologica.

[Unilateral aplasia of kidney and ureter in both of identical twins].

P. J. Waardenburg, 1952, Acta geneticae medicae et gemellologiae.

Different types of hereditary optic atrophy.

P. J. Waardenburg, 1957, Acta genetica et statistica medica.

The twin-study method in wider perspective.

P. J. Waardenburg, 1957, Acta genetica et statistica medica.

Squint and heredity

P. J. Waardenburg, 2004, Documenta Ophthalmologica.

Does agenesis or dysgenesis neuroepithelialis retinae, whether or not related to keratoglobus, exist?

P. J. Waardenburg, 1957, Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde.

Intermarriages of hereditarily deaf mute and of hereditarily blind people, marriage counselling and the question of sterilization.

P. J. Waardenburg, 1956, Acta genetica et statistica medica.

Gross remnants of the pupillary membrane, anterior polar cataract and microcornea in a mother and her children.

P. J. Waardenburg, 1949, Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde.

Ocular disturbances in encephalitis lethargica

P. J. Waardenburg, 1921 .

BLOOD COAGULATION IN EPIDERMOLYSIS BULLOSA HEREDITARIA. GENETIC OBSERVATIONS.

H. Vermeulen, P. J. Waardenburg, T. H. Tio, 1963, Archives of dermatology.

NYSTAGMOGRAPHICAL STUDIES IN ALAND EYE DISEASE

A. Eriksson, H. Forsius, A. V. Vliet, 1973, Monographs in human genetics.

Nystagmographical studies in Aland eye disease.

A. Eriksson, H. Forsius, P. J. Waardenburg, 1972, Acta ophthalmologica.

Some notes on publications of Professor Arnold Sorsby and on Aland eye disease (Forsius-Eriksson syndrome).

P. J. Waardenburg, 1970, Journal of Medical Genetics.