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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.
American Journal of Medical Genetics
|
November 1, 1988
Mosaic trisomy 7 confined to the placenta
M J McKinley, L U Kearney, K H Nicolaides, et al.
Molecular Reproduction and Development
|
January 1, 1989
Sexing the human fetus and identification of polyploid nuclei by DNA-DNA in situ hybridisation in interphase nuclei
J D West, C M Gosden, J R Gosden, et al.
Fetal Therapy
|
January 1, 1989
Mean red cell volume in normal, anemic, small, trisomic and triploid fetuses
K H Nicolaides, R J Snijders, J G Thorpe-Beeston, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
April 1, 1995
Identifying genes within microdissected genomic DNA: isolation of brain expressed genes from a translocation region associated with inherited mental illness
A J Brookes, E M Slorach, K L Evans, et al.
British Journal of Obstetrics and Gynaecology
|
July 1, 1985
Fetoscopy in the assessment of unexplained fetal hydrops
K H Nicolaides, C H Rodeck, I Lange, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 63) with videos related to
Sort By:
Page
of 7
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.
American Journal of Medical Genetics
|
November 1, 1988
Mosaic trisomy 7 confined to the placenta
M J McKinley, L U Kearney, K H Nicolaides, et al.
Molecular Reproduction and Development
|
January 1, 1989
Sexing the human fetus and identification of polyploid nuclei by DNA-DNA in situ hybridisation in interphase nuclei
J D West, C M Gosden, J R Gosden, et al.
Fetal Therapy
|
January 1, 1989
Mean red cell volume in normal, anemic, small, trisomic and triploid fetuses
K H Nicolaides, R J Snijders, J G Thorpe-Beeston, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
April 1, 1995
Identifying genes within microdissected genomic DNA: isolation of brain expressed genes from a translocation region associated with inherited mental illness
A J Brookes, E M Slorach, K L Evans, et al.
British Journal of Obstetrics and Gynaecology
|
July 1, 1985
Fetoscopy in the assessment of unexplained fetal hydrops
K H Nicolaides, C H Rodeck, I Lange, et al.
Page
of 7