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Experientia
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August 15, 1977
Sister chromatid exchanges in human lymphocytes exposed to 8-methoxypsoralen and long wave UV radiation prior to incorporation of bromodeoxyuridine
D Mourelatos, M J Faed, B E Johnson
Journal of Medical Genetics
|
February 1, 1982
Cytogenetic and histological studies of testicular biopsies from subfertile men with chromosome anomaly
M J Faed, M A Lamont, K Baxby
The British Journal of Dermatology
|
May 1, 1983
In vitro growth rates of epidermal cells derived from the skin of psoriatic patients and non-psoriatic controls
M R West, K J Kenicer, M J Faed
Human Genetics
|
January 1, 1983
Chromosome abnormality in couples with histories of multiple abortions. The outcome of pregnancies subsequent to ascertainment and a study of familial translocation carriers
J Wolstenholme, M J Faed, J Robertson, et al.
Journal of Medical Genetics
|
December 1, 1982
Isodicentric X chromosome in a moderately tall patient with gonadal dysgenesis: lack of effect of functional centromere on inactivation pattern
J Robertson, M J Faed, M A Lamont, et al.
Prenatal Diagnosis
|
January 1, 1983
Amylo-1,6-glucosidase activity in cultured cells: a deficiency in type III glycogenosis with prenatal studies
G T Besley, P T Cohen, M J Faed, et al.
Clinical Genetics
|
September 1, 1979
A chromosome survey of a hospital for the mentally subnormal
M J Faed, J Robertson, M A Field, et al.
Archives of Disease in Childhood
|
February 1, 1991
45,X/46,X dic (Y) mosaicism in a phenotypic male
P J Batstone, M J Faed, R T Jung, et al.
British Journal of Cancer
|
May 1, 1983
Incidence of familial Hodgkin's disease
L Kerzin-Storrar, M J Faed, J B MacGillivray, et al.
Clinical Genetics
|
October 1, 1978
An XYY boy with short stature and a case of Klinefelter's syndrome (XXY) in a family with inversion 9
M J Faed, M Lamont, H G Morton, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 34) with videos related to
Sort By:
Page
of 4
Experientia
|
August 15, 1977
Sister chromatid exchanges in human lymphocytes exposed to 8-methoxypsoralen and long wave UV radiation prior to incorporation of bromodeoxyuridine
D Mourelatos, M J Faed, B E Johnson
Journal of Medical Genetics
|
February 1, 1982
Cytogenetic and histological studies of testicular biopsies from subfertile men with chromosome anomaly
M J Faed, M A Lamont, K Baxby
The British Journal of Dermatology
|
May 1, 1983
In vitro growth rates of epidermal cells derived from the skin of psoriatic patients and non-psoriatic controls
M R West, K J Kenicer, M J Faed
Human Genetics
|
January 1, 1983
Chromosome abnormality in couples with histories of multiple abortions. The outcome of pregnancies subsequent to ascertainment and a study of familial translocation carriers
J Wolstenholme, M J Faed, J Robertson, et al.
Journal of Medical Genetics
|
December 1, 1982
Isodicentric X chromosome in a moderately tall patient with gonadal dysgenesis: lack of effect of functional centromere on inactivation pattern
J Robertson, M J Faed, M A Lamont, et al.
Prenatal Diagnosis
|
January 1, 1983
Amylo-1,6-glucosidase activity in cultured cells: a deficiency in type III glycogenosis with prenatal studies
G T Besley, P T Cohen, M J Faed, et al.
Clinical Genetics
|
September 1, 1979
A chromosome survey of a hospital for the mentally subnormal
M J Faed, J Robertson, M A Field, et al.
Archives of Disease in Childhood
|
February 1, 1991
45,X/46,X dic (Y) mosaicism in a phenotypic male
P J Batstone, M J Faed, R T Jung, et al.
British Journal of Cancer
|
May 1, 1983
Incidence of familial Hodgkin's disease
L Kerzin-Storrar, M J Faed, J B MacGillivray, et al.
Clinical Genetics
|
October 1, 1978
An XYY boy with short stature and a case of Klinefelter's syndrome (XXY) in a family with inversion 9
M J Faed, M Lamont, H G Morton, et al.
Page
of 4