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F L Raymond

Showing results (1-10 of 26) with videos related to

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Developmental Medicine and Child Neurology|June 1, 1997
Spinal muscular atrophy of childhood: geneticsF L Raymond
Journal of Medical Genetics|August 25, 2005
X linked mental retardation: a clinical guideF L Raymond
Journal of Intellectual Disability Research : JIDR|September 17, 2003
Genetic services for people with intellectual disability and their familiesF L Raymond
Clinical Genetics|November 22, 2011
Genetic testing and screening of individuals at risk of NF2D G Evans, F L Raymond, J G Barwell, et al.
Heart (British Cardiac Society)|December 1, 1996
Isomerism of the atrial appendages associated with 22q11 deletion in a fetusR W Yates, F L Raymond, A Cook, et al.
Journal of Medical Genetics|August 1, 1997
Prenatal diagnosis of 22q11 deletions: a series of five cases with congenital heart defectsF L Raymond, J M Simpson, C M Mackie, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|September 17, 2002
Hypophosphatasia associated with increased nuchal translucency: a report of two affected pregnanciesA P Souka, F L Raymond, E Mornet, et al.
Lancet (London, England)|October 7, 1997
Fetal echocardiography as a predictor of chromosomal abnormalityF L Raymond, J M Simpson, G K Sharland, et al.
Clinical Genetics|December 12, 2007
Restoring reproductive confidence in families with X-linked mental retardation by finding the causal mutationG Turner, J Boyle, M W Partington, et al.
Journal of Medical Genetics|March 8, 2003
Identification of a 650 kb duplication at the X chromosome breakpoint in a patient with 46,X,t(X;8)(q28;q12) and non-syndromic mental retardationJ J Cox, S T Holden, S Dee, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Developmental Medicine and Child Neurology|June 1, 1997
Spinal muscular atrophy of childhood: geneticsF L Raymond
Journal of Medical Genetics|August 25, 2005
X linked mental retardation: a clinical guideF L Raymond
Journal of Intellectual Disability Research : JIDR|September 17, 2003
Genetic services for people with intellectual disability and their familiesF L Raymond
Clinical Genetics|November 22, 2011
Genetic testing and screening of individuals at risk of NF2D G Evans, F L Raymond, J G Barwell, et al.
Heart (British Cardiac Society)|December 1, 1996
Isomerism of the atrial appendages associated with 22q11 deletion in a fetusR W Yates, F L Raymond, A Cook, et al.
Journal of Medical Genetics|August 1, 1997
Prenatal diagnosis of 22q11 deletions: a series of five cases with congenital heart defectsF L Raymond, J M Simpson, C M Mackie, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|September 17, 2002
Hypophosphatasia associated with increased nuchal translucency: a report of two affected pregnanciesA P Souka, F L Raymond, E Mornet, et al.
Lancet (London, England)|October 7, 1997
Fetal echocardiography as a predictor of chromosomal abnormalityF L Raymond, J M Simpson, G K Sharland, et al.
Clinical Genetics|December 12, 2007
Restoring reproductive confidence in families with X-linked mental retardation by finding the causal mutationG Turner, J Boyle, M W Partington, et al.
Journal of Medical Genetics|March 8, 2003
Identification of a 650 kb duplication at the X chromosome breakpoint in a patient with 46,X,t(X;8)(q28;q12) and non-syndromic mental retardationJ J Cox, S T Holden, S Dee, et al.
Pageof 3