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g r fraser
g r fraser
retired professor of human genetics
Geverifieerd e-mailadres voor doctors.org.uk
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Murderous science: Elimination by scientific selection of Jews, Gypsies, and others, Germany 1933-1945
B Müller-Hill, GR Fraser
Oxford University Press, 1988
8311988
The causes of profound deafness in childhood: a study of 3,535 individuals with severe hearing loss present at birth or of childhood onset
GR Fraser
(No Title), 1976
3921976
Association of congenital deafness with goitre (Pendred's syndrome).
GR Fraser
Annals of human genetics, 1965
3061965
Congenital deafness associated with electrocardiographic abnormalities, fainting attacks and sudden death: a recessive syndrome
GR Fraser, P Froggatt, TN James
QJM: An International Journal of Medicine 33 (3), 361-385, 1964
2851964
Our genetical ‘load’. A review of some aspects of genetical variation
GR Fraser
Annals of Human Genetics 25 (4), 387-415, 1962
2361962
Profound childhood deafness
GR Fraser
Journal of Medical Genetics 1 (2), 118, 1964
2301964
Cleft lip and palate: seasonal incidence, birth weight, birth rank, sex, site, associated malformations and parental age: A statistical survey
GR Fraser, JS Calnan
Archives of disease in childhood 36 (188), 420, 1961
2121961
Genetical aspects of the cardio‐auditory syndrome of Jervell and Lange‐Nielsen (congenital deafness and electrocardiographic abnormalities)
GR Fraser, P Froggatt, T Murphy
Annals of human genetics 28 (1‐3), 133-157, 1964
1741964
The Causes of Blindness in Childhood; A Study of 776 Children with Severe Visual Handicaps.
GR Fraser, AI Friedman
The Johns Hopkins Press, Baltimore, Maryland 21218, 1968
1711968
Pathology of the ear in the cardio-auditory syndrome of Jervell and Lange-Nielsen (recessive deafness with electrocardiographic abnormalities)
I Friedmann, GR Fraser, P Froggatt
The Journal of Laryngology & Otology 80 (5), 451-470, 1966
169*1966
The syndrome of sporadic goitre and congenital deafness
GR Fraser, ME Morgans, WR Trotter
QJM: An International Journal of Medicine 29 (2), 279-295, 1960
1641960
Family studies on ocular refraction and its components
A Sorsby, GA Leary, GR Fraser
Journal of Medical Genetics 3 (4), 269, 1966
1271966
The Causes of Blindness in Childhood; A Study of 776 Children with Severe Visual Handicaps.
GR Fraser, AI Friedman
The Johns Hopkins Press, Baltimore, Maryland 21218, 1968
1221968
The association of juvenile diabetes mellitus and optic atrophy: clinical and genetical aspects
FC Rose, GR Fraser, AI Friedmann, EM Kohner
QJM: An International Journal of Medicine 35 (3), 385-405, 1966
1101966
Population genetic studies in the Congo. I. Glucose-6-phosphate dehydrogenase deficiency, hemoglobin S, and malaria.
AG Motulsky, J Vandepitte, GR Fraser
American Journal of Human Genetics 18 (6), 514, 1966
941966
On the familial predisposition to favism.
G Stamatoyannopoulos, GR Fraser, AC Motulsky, P Fessas, A Akrivakis, ...
American Journal of Human Genetics 18 (3), 253, 1966
771966
Public health and long-term genetic implications of intrauterine diagnosis and selective abortion
AG Motulsky, GR Fraser, J Felsenstein
Birth defects original article series 7 (5), 22-32, 1971
761971
Sex‐linked recessive congenital deafness and the excess of males in profound childhood deafness
GR Fraser
Annals of Human Genetics 29 (2), 171-196, 1965
751965
Cretinism and taste sensitivity to phenylthiocarbamide
GR Fraser
The Lancet 277 (7184), 964-965, 1961
741961
Common variable immunodeficiency, Hodgkin's disease, and other malignancies in a Newfoundland family
SK Buehler, G Fodor, WH Marshall, F Firme, GR Fraser, P Vaze
The Lancet 305 (7900), 195-197, 1975
711975
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Artikelen 1–20