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N C Nevin

Showing results (51-60 of 223) with videos related to

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British Medical Journal|August 21, 1976
Letter: Raised alpha-fetoprotein levels and congenital defectN C Nevin, W Thompson, G Roberts
Clinical Genetics|May 1, 1979
Trisomy 20 mosaicism in amniotic fluid cell cultureN C Nevin, J Nevin, W Thompson
Lancet (London, England)|July 17, 1971
Isolated absence of IgA with autosomal dominant inheritanceG H Tomkin, M Mawhinney, N C Nevin
Clinical Dysmorphology|April 1, 1994
An 18 week fetus with Elejalde syndrome (acrocephalopolydactylyous dysplasia)N C Nevin, B Herron, M J Armstrong
Developmental Medicine and Child Neurology|August 1, 1982
Family study of congenital hydrocephalusC Adams, W P Johnston, N C Nevin
Irish Journal of Medical Science|August 13, 2016
Quantitative nitroblue tetrazolium test in mongolismN Johnston, J B Bridges, N C Nevin
American Journal of Medical Genetics|May 1, 1986
Syndrome of short stature, microcephaly, mental retardation, and multiple epiphyseal dysplasia--Lowry-Wood syndromeN C Nevin, P S Thomas, J Hutchinson
Journal of Medical Genetics|June 1, 1971
A child with a ring G chromosome (46,XX, Gr)N C Nevin, B MacLaverty, W A Campbell
American Journal of Medical Genetics|November 15, 1994
Polydactyly in a carrier of the gene for the Meckel syndromeJ Nelson, N C Nevin, E J Hanna
Irish Journal of Medical Science|July 1, 1971
An unusual case of chronic granulocytic leukaemiaA Redmond, N C Nevin, J M Bridges
Pageof 23

Showing results (51-60 of 223) with videos related to

Sort By:
Pageof 23
British Medical Journal|August 21, 1976
Letter: Raised alpha-fetoprotein levels and congenital defectN C Nevin, W Thompson, G Roberts
Clinical Genetics|May 1, 1979
Trisomy 20 mosaicism in amniotic fluid cell cultureN C Nevin, J Nevin, W Thompson
Lancet (London, England)|July 17, 1971
Isolated absence of IgA with autosomal dominant inheritanceG H Tomkin, M Mawhinney, N C Nevin
Clinical Dysmorphology|April 1, 1994
An 18 week fetus with Elejalde syndrome (acrocephalopolydactylyous dysplasia)N C Nevin, B Herron, M J Armstrong
Developmental Medicine and Child Neurology|August 1, 1982
Family study of congenital hydrocephalusC Adams, W P Johnston, N C Nevin
Irish Journal of Medical Science|August 13, 2016
Quantitative nitroblue tetrazolium test in mongolismN Johnston, J B Bridges, N C Nevin
American Journal of Medical Genetics|May 1, 1986
Syndrome of short stature, microcephaly, mental retardation, and multiple epiphyseal dysplasia--Lowry-Wood syndromeN C Nevin, P S Thomas, J Hutchinson
Journal of Medical Genetics|June 1, 1971
A child with a ring G chromosome (46,XX, Gr)N C Nevin, B MacLaverty, W A Campbell
American Journal of Medical Genetics|November 15, 1994
Polydactyly in a carrier of the gene for the Meckel syndromeJ Nelson, N C Nevin, E J Hanna
Irish Journal of Medical Science|July 1, 1971
An unusual case of chronic granulocytic leukaemiaA Redmond, N C Nevin, J M Bridges
Pageof 23