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BMJ (Clinical Research Ed.)
|
June 20, 1998
Embryonic abnormalities at medical termination of pregnancy with mifepristone and misoprostol during first trimester: observational study
G Blanch, S Quenby, E S Ballantyne, et al.
International Journal of Oncology
|
February 10, 1998
The Knights of the Round Table hypothesis of tumour suppressor gene function--noble sacrifice or sexual dalliance: genes, including p53, BRCA1/2 and RB have evolved by horizontal and vertical transmission of mating factor genes and are involved in gametogenesis, implantation, development and tumourigenesis
C M Gosden, T Liloglou, J Nunn, et al.
Human Genetics
|
January 1, 1984
The use of cloned Y chromosome-specific DNA probes for fetal sex determination in first trimester prenatal diagnosis
J R Gosden, C M Gosden, S Christie, et al.
Prenatal Diagnosis
|
June 1, 1994
Prenatal diagnosis of fragile X syndrome: management of the male fetus with a premutation
L Strain, M E Porteous, C M Gosden, et al.
Lancet (London, England)
|
December 10, 1983
A single-operator technique for first-trimester chorion biopsy
C H Rodeck, J M Morsman, K H Nicolaides, et al.
Journal of Medical Genetics
|
February 1, 1986
Prenatal diagnosis of bullous ichthyosiform erythroderma: detection of tonofilament clumps in fetal epidermal and amniotic fluid cells
R A Eady, D B Gunner, L D Carbone, et al.
British Journal of Obstetrics and Gynaecology
|
September 1, 1995
How acute is the acute shortage of oocyte donors in the UK? Results of a British national survey
M M Biljan, C T Taylor, C M Gosden, et al.
American Journal of Medical Genetics
|
May 1, 1988
Prenatal diagnosis of fragile X syndrome by placental (chorionic villi) biopsy culture
M J McKinley, L U Kearney, K H Nicolaides, et al.
Journal of Pediatric Surgery
|
August 31, 1999
Ontogeny of interstitial cells of Cajal in the human intestine
S E Kenny, G Connell, M N Woodward, et al.
Human Genetics
|
June 1, 1987
Ten families with fragile X syndrome: linkage relationships with four DNA probes from distal Xq
J A Buchanan, K E Buckton, C M Gosden, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 56) with videos related to
Sort By:
Page
of 6
BMJ (Clinical Research Ed.)
|
June 20, 1998
Embryonic abnormalities at medical termination of pregnancy with mifepristone and misoprostol during first trimester: observational study
G Blanch, S Quenby, E S Ballantyne, et al.
International Journal of Oncology
|
February 10, 1998
The Knights of the Round Table hypothesis of tumour suppressor gene function--noble sacrifice or sexual dalliance: genes, including p53, BRCA1/2 and RB have evolved by horizontal and vertical transmission of mating factor genes and are involved in gametogenesis, implantation, development and tumourigenesis
C M Gosden, T Liloglou, J Nunn, et al.
Human Genetics
|
January 1, 1984
The use of cloned Y chromosome-specific DNA probes for fetal sex determination in first trimester prenatal diagnosis
J R Gosden, C M Gosden, S Christie, et al.
Prenatal Diagnosis
|
June 1, 1994
Prenatal diagnosis of fragile X syndrome: management of the male fetus with a premutation
L Strain, M E Porteous, C M Gosden, et al.
Lancet (London, England)
|
December 10, 1983
A single-operator technique for first-trimester chorion biopsy
C H Rodeck, J M Morsman, K H Nicolaides, et al.
Journal of Medical Genetics
|
February 1, 1986
Prenatal diagnosis of bullous ichthyosiform erythroderma: detection of tonofilament clumps in fetal epidermal and amniotic fluid cells
R A Eady, D B Gunner, L D Carbone, et al.
British Journal of Obstetrics and Gynaecology
|
September 1, 1995
How acute is the acute shortage of oocyte donors in the UK? Results of a British national survey
M M Biljan, C T Taylor, C M Gosden, et al.
American Journal of Medical Genetics
|
May 1, 1988
Prenatal diagnosis of fragile X syndrome by placental (chorionic villi) biopsy culture
M J McKinley, L U Kearney, K H Nicolaides, et al.
Journal of Pediatric Surgery
|
August 31, 1999
Ontogeny of interstitial cells of Cajal in the human intestine
S E Kenny, G Connell, M N Woodward, et al.
Human Genetics
|
June 1, 1987
Ten families with fragile X syndrome: linkage relationships with four DNA probes from distal Xq
J A Buchanan, K E Buckton, C M Gosden, et al.
Page
of 6