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Lancet (London, England)
|
December 19, 1981
Vitamin supplementation and neural tube defects
R W Smithells, S Sheppard, C J Schorah, et al.
Human Molecular Genetics
|
February 1, 1994
Genetic linkage of familial expansile osteolysis to chromosome 18q
A E Hughes, A M Shearman, J L Weber, et al.
Archives of Disease in Childhood
|
February 24, 2000
Effect of genotype on changes in intelligence quotient after dietary relaxation in phenylketonuria and hyperphenylalaninaemia
L G Greeves, C C Patterson, D J Carson, et al.
British Medical Journal
|
May 15, 1971
Dysgammaglobulinaemia complicated by disseminated measles
H Mawhinney, I V Allen, J M Beare, et al.
Lancet (London, England)
|
May 7, 1983
Further experience of vitamin supplementation for prevention of neural tube defect recurrences
R W Smithells, N C Nevin, M J Seller, et al.
Archives of Disease in Childhood
|
May 1, 1986
Recurrent neural tube defects, risk factors and vitamins
J Wild, A P Read, S Sheppard, et al.
British Journal of Obstetrics and Gynaecology
|
February 1, 1985
Neural-tube defects and vitamins: the need for a randomized clinical trial
R W Smithells, S Sheppard, J Wild, et al.
The Journal of Bone and Joint Surgery. British Volume
|
March 1, 1988
Familial expansile osteolysis. A new dysplasia
P H Osterberg, R G Wallace, D A Adams, et al.
Human Heredity
|
February 15, 2001
Additional glomangioma families link to chromosome 1p: no evidence for genetic heterogeneity
J T Calvert, S Burns, T J Riney, et al.
Journal of Medical Genetics
|
August 1, 1997
Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosis
W Reardon, D Wilkes, P Rutland, et al.
Page
of 23
Search research articles
Search
Showing results (211-220 of 223) with videos related to
Sort By:
Page
of 23
Lancet (London, England)
|
December 19, 1981
Vitamin supplementation and neural tube defects
R W Smithells, S Sheppard, C J Schorah, et al.
Human Molecular Genetics
|
February 1, 1994
Genetic linkage of familial expansile osteolysis to chromosome 18q
A E Hughes, A M Shearman, J L Weber, et al.
Archives of Disease in Childhood
|
February 24, 2000
Effect of genotype on changes in intelligence quotient after dietary relaxation in phenylketonuria and hyperphenylalaninaemia
L G Greeves, C C Patterson, D J Carson, et al.
British Medical Journal
|
May 15, 1971
Dysgammaglobulinaemia complicated by disseminated measles
H Mawhinney, I V Allen, J M Beare, et al.
Lancet (London, England)
|
May 7, 1983
Further experience of vitamin supplementation for prevention of neural tube defect recurrences
R W Smithells, N C Nevin, M J Seller, et al.
Archives of Disease in Childhood
|
May 1, 1986
Recurrent neural tube defects, risk factors and vitamins
J Wild, A P Read, S Sheppard, et al.
British Journal of Obstetrics and Gynaecology
|
February 1, 1985
Neural-tube defects and vitamins: the need for a randomized clinical trial
R W Smithells, S Sheppard, J Wild, et al.
The Journal of Bone and Joint Surgery. British Volume
|
March 1, 1988
Familial expansile osteolysis. A new dysplasia
P H Osterberg, R G Wallace, D A Adams, et al.
Human Heredity
|
February 15, 2001
Additional glomangioma families link to chromosome 1p: no evidence for genetic heterogeneity
J T Calvert, S Burns, T J Riney, et al.
Journal of Medical Genetics
|
August 1, 1997
Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosis
W Reardon, D Wilkes, P Rutland, et al.
Page
of 23