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BMJ (Clinical Research Ed.)
|
July 17, 1993
Case-control study of congenital anomalies in children of cancer patients
L Dodds, L D Marrett, D J Tomkins, et al.
Occupational and Environmental Medicine
|
January 10, 1998
Risk of congenital anomalies in children of parents occupationally exposed to low level ionising radiation
L M Green, L Dodds, A B Miller, et al.
Experimental Cell Research
|
December 1, 1986
Transformation of human cultured fibroblasts with plasmids carrying dominant selection markers and immortalizing potential
P L Chang, J L Gunby, D J Tomkins, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1996
Maternal uniparental isodisomy of human chromosome 14 associated with a paternal t(13q14q) and precocious puberty
D J Tomkins, A F Roux, J Waye, et al.
Clinical Genetics
|
June 14, 2000
Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency
M J Nowaczyk, M J Huggins, D J Tomkins, et al.
Prenatal Diagnosis
|
July 27, 1999
Cytogenetic aspects of the Canadian early and mid-trimester amniotic fluid trial (CEMAT)
E J Winsor, D J Tomkins, D Kalousek, et al.
Nature Genetics
|
April 1, 1996
Inactivation of Fac in mice produces inducible chromosomal instability and reduced fertility reminiscent of Fanconi anaemia
M Chen, D J Tomkins, W Auerbach, et al.
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Search research articles
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Showing results (21-30 of 27) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 27 results.
BMJ (Clinical Research Ed.)
|
July 17, 1993
Case-control study of congenital anomalies in children of cancer patients
L Dodds, L D Marrett, D J Tomkins, et al.
Occupational and Environmental Medicine
|
January 10, 1998
Risk of congenital anomalies in children of parents occupationally exposed to low level ionising radiation
L M Green, L Dodds, A B Miller, et al.
Experimental Cell Research
|
December 1, 1986
Transformation of human cultured fibroblasts with plasmids carrying dominant selection markers and immortalizing potential
P L Chang, J L Gunby, D J Tomkins, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1996
Maternal uniparental isodisomy of human chromosome 14 associated with a paternal t(13q14q) and precocious puberty
D J Tomkins, A F Roux, J Waye, et al.
Clinical Genetics
|
June 14, 2000
Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency
M J Nowaczyk, M J Huggins, D J Tomkins, et al.
Prenatal Diagnosis
|
July 27, 1999
Cytogenetic aspects of the Canadian early and mid-trimester amniotic fluid trial (CEMAT)
E J Winsor, D J Tomkins, D Kalousek, et al.
Nature Genetics
|
April 1, 1996
Inactivation of Fac in mice produces inducible chromosomal instability and reduced fertility reminiscent of Fanconi anaemia
M Chen, D J Tomkins, W Auerbach, et al.
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of 3