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L Brueton

Showing results (1-10 of 22) with videos related to

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European Journal of Medical Genetics|February 21, 2006
Partial trisomy 17p12pter, associated with pre and postnatal growth retardation, dysmorphic facial and digital features, developmental delay, and signs of HMSN1 in early childhoodJ Vogt, S Hill, L Brueton
Lancet (London, England)|July 31, 1993
Homozygous nonsense mutation in the insulin receptor gene in infant with leprechaunismA Krook, L Brueton, S O'Rahilly
Lancet (London, England)|July 21, 1990
Genetic counselling for cystic fibrosis based upon mutation/haplotype analysisE Watson, B Williamson, L Brueton, et al.
Journal of Plastic, Reconstructive & Aesthetic Surgery : JPRAS|March 14, 2007
Hypoplastic thumb in Gorlin's syndromeA Kansal, L Brueton, A Lahiri, et al.
American Journal of Medical Genetics|December 1, 1988
Chromosomal localisation of a developmental gene in man: direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13L Brueton, S M Huson, R M Winter, et al.
Prenatal Diagnosis|July 1, 1995
Prenatal analysis of the insulin receptor gene in a family with leprechaunismA Krook, J A Bell, M E Robertson, et al.
Lancet (London, England)|July 1, 1995
Arthrogryposis multiplex congenita with maternal autoantibodies specific for a fetal antigenA Vincent, C Newland, L Brueton, et al.
Clinical Genetics|November 15, 2000
Imprinting centre deletions in two PWS families: implications for diagnostic testing and genetic counselingK Buiting, C Färber, P Kroisel, et al.
Prenatal Diagnosis|July 22, 2005
Omphalopagus conjoining and twin-twin transfusion syndromeJ C Y Chan, D A Somerset, N Ostojic, et al.
Clinical Genetics|April 19, 2011
Screening and cell-based assessment of mutations in the Aristaless-related homeobox (ARX) geneT Fullston, M Finnis, A Hackett, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
European Journal of Medical Genetics|February 21, 2006
Partial trisomy 17p12pter, associated with pre and postnatal growth retardation, dysmorphic facial and digital features, developmental delay, and signs of HMSN1 in early childhoodJ Vogt, S Hill, L Brueton
Lancet (London, England)|July 31, 1993
Homozygous nonsense mutation in the insulin receptor gene in infant with leprechaunismA Krook, L Brueton, S O'Rahilly
Lancet (London, England)|July 21, 1990
Genetic counselling for cystic fibrosis based upon mutation/haplotype analysisE Watson, B Williamson, L Brueton, et al.
Journal of Plastic, Reconstructive & Aesthetic Surgery : JPRAS|March 14, 2007
Hypoplastic thumb in Gorlin's syndromeA Kansal, L Brueton, A Lahiri, et al.
American Journal of Medical Genetics|December 1, 1988
Chromosomal localisation of a developmental gene in man: direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13L Brueton, S M Huson, R M Winter, et al.
Prenatal Diagnosis|July 1, 1995
Prenatal analysis of the insulin receptor gene in a family with leprechaunismA Krook, J A Bell, M E Robertson, et al.
Lancet (London, England)|July 1, 1995
Arthrogryposis multiplex congenita with maternal autoantibodies specific for a fetal antigenA Vincent, C Newland, L Brueton, et al.
Clinical Genetics|November 15, 2000
Imprinting centre deletions in two PWS families: implications for diagnostic testing and genetic counselingK Buiting, C Färber, P Kroisel, et al.
Prenatal Diagnosis|July 22, 2005
Omphalopagus conjoining and twin-twin transfusion syndromeJ C Y Chan, D A Somerset, N Ostojic, et al.
Clinical Genetics|April 19, 2011
Screening and cell-based assessment of mutations in the Aristaless-related homeobox (ARX) geneT Fullston, M Finnis, A Hackett, et al.
Pageof 3