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British Journal of Obstetrics and Gynaecology
|
March 1, 1994
Investigation of folate intake and metabolism in women who have had two pregnancies complicated by neural tube defects
J Wild, M J Seller, C J Schorah, et al.
Experimental and Clinical Immunogenetics
|
January 1, 1990
Alpha-fetoprotein levels in different strains of mice during development
M Adinolfi, S E Beck, M J Seller, et al.
Journal of Medical Genetics
|
December 1, 1976
Levels of alpha-fetoprotein in amniotic fluids of mice (curly-tail) with neural tube defects
M Adinolfi, S Beck, S Embury, et al.
Clinical Dysmorphology
|
April 18, 1998
Cerebellar hypoplasia, facial dysmorphism and internal abnormalities: a new recessive syndrome?
M J Seller, K Pal, G Moscoso, et al.
American Journal of Medical Genetics
|
December 1, 1992
Chondrodysplasia punctata: another possible X-linked recessive case
C P Bennett, A C Berry, D J Maxwell, et al.
Clinical Dysmorphology
|
January 1, 1997
Phenotypic diversity in the Smith-Lemli-Opitz syndrome
M J Seller, F A Flinter, Z Docherty, et al.
Genomics
|
June 13, 2001
Physical and transcript map of the dominant optic atrophy (OPA1) gene critical region at 3q28-q29
J T Behnam, C Hamer, D Spalton, et al.
Journal of Medical Genetics
|
December 10, 1997
Rapid identification of multiple supernumerary ring chromosomes with a new FISH technique
C Mackie-Ogilvie, K Waddle, J Mandeville, et al.
British Journal of Obstetrics and Gynaecology
|
June 1, 1980
Amniotic fluid acetylcholinesterase and prenatal diagnosis
M J Seller, K J Cole, A H Fensom, et al.
Clinical Dysmorphology
|
July 1, 1996
A new lethal chondrodysplasia with platyspondyly, long bone angulation and mixed bone density
M J Seller, A C Berry, D Maxwell, et al.
Page
of 8
Search research articles
Search
Showing results (51-60 of 80) with videos related to
Sort By:
Page
of 8
British Journal of Obstetrics and Gynaecology
|
March 1, 1994
Investigation of folate intake and metabolism in women who have had two pregnancies complicated by neural tube defects
J Wild, M J Seller, C J Schorah, et al.
Experimental and Clinical Immunogenetics
|
January 1, 1990
Alpha-fetoprotein levels in different strains of mice during development
M Adinolfi, S E Beck, M J Seller, et al.
Journal of Medical Genetics
|
December 1, 1976
Levels of alpha-fetoprotein in amniotic fluids of mice (curly-tail) with neural tube defects
M Adinolfi, S Beck, S Embury, et al.
Clinical Dysmorphology
|
April 18, 1998
Cerebellar hypoplasia, facial dysmorphism and internal abnormalities: a new recessive syndrome?
M J Seller, K Pal, G Moscoso, et al.
American Journal of Medical Genetics
|
December 1, 1992
Chondrodysplasia punctata: another possible X-linked recessive case
C P Bennett, A C Berry, D J Maxwell, et al.
Clinical Dysmorphology
|
January 1, 1997
Phenotypic diversity in the Smith-Lemli-Opitz syndrome
M J Seller, F A Flinter, Z Docherty, et al.
Genomics
|
June 13, 2001
Physical and transcript map of the dominant optic atrophy (OPA1) gene critical region at 3q28-q29
J T Behnam, C Hamer, D Spalton, et al.
Journal of Medical Genetics
|
December 10, 1997
Rapid identification of multiple supernumerary ring chromosomes with a new FISH technique
C Mackie-Ogilvie, K Waddle, J Mandeville, et al.
British Journal of Obstetrics and Gynaecology
|
June 1, 1980
Amniotic fluid acetylcholinesterase and prenatal diagnosis
M J Seller, K J Cole, A H Fensom, et al.
Clinical Dysmorphology
|
July 1, 1996
A new lethal chondrodysplasia with platyspondyly, long bone angulation and mixed bone density
M J Seller, A C Berry, D Maxwell, et al.
Page
of 8