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M Pembrey

Showing results (11-20 of 48) with videos related to

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European Journal of Human Genetics : EJHG|January 15, 1999
Chinese amend policy on sterilisation for genetic reasonsM Pembrey, S Aymé
Archives of Disease in Childhood|November 1, 1990
The genetics of deafnessW Reardon, M Pembrey
The British Journal of Psychiatry : the Journal of Mental Science|August 3, 2001
Hyperphagic short stature and Prader--Willi syndrome: a comparison of behavioural phenotypes, genotypes and indices of stressJ Gilmour, D Skuse, M Pembrey
Paediatric and Perinatal Epidemiology|March 10, 2001
ALSPAC--the Avon Longitudinal Study of Parents and Children. I. Study methodologyJ Golding, M Pembrey, R Jones, et al.
Clinical Dysmorphology|July 1, 1993
Okihiro syndrome: thenar hypoplasia and Duane anomaly in three generationsA Collins, M Baraitser, M Pembrey
Journal of Medical Genetics|October 1, 1985
Phenotypic variation in LADD syndromeE Thompson, M Pembrey, J M Graham
Journal of Intellectual Disability Research : JIDR|February 1, 1994
Fragile-X syndrome in North East Essex: towards systematic screening: clinical selectionM Sabaratnam, S Laver, L Butler, et al.
Journal of Intellectual Disability Research : JIDR|March 24, 1999
Diagnosis of fragile-X syndrome: the experiences of parentsB Carmichael, M Pembrey, G Turner, et al.
Archives of Disease in Childhood|March 1, 1981
Sickle cell disease in Saudi Arabs in early childhoodR P Perrine, P John, M Pembrey, et al.
Lancet (London, England)|May 8, 1999
Mitochondrial 16189 variant, thinness at birth, and type-2 diabetes. ALSPAC study team. Avon Longitudinal Study of Pregnancy and ChildhoodK Casteels, K Ong, D Phillips, et al.
Pageof 5

Showing results (11-20 of 48) with videos related to

Sort By:
Pageof 5
European Journal of Human Genetics : EJHG|January 15, 1999
Chinese amend policy on sterilisation for genetic reasonsM Pembrey, S Aymé
Archives of Disease in Childhood|November 1, 1990
The genetics of deafnessW Reardon, M Pembrey
The British Journal of Psychiatry : the Journal of Mental Science|August 3, 2001
Hyperphagic short stature and Prader--Willi syndrome: a comparison of behavioural phenotypes, genotypes and indices of stressJ Gilmour, D Skuse, M Pembrey
Paediatric and Perinatal Epidemiology|March 10, 2001
ALSPAC--the Avon Longitudinal Study of Parents and Children. I. Study methodologyJ Golding, M Pembrey, R Jones, et al.
Clinical Dysmorphology|July 1, 1993
Okihiro syndrome: thenar hypoplasia and Duane anomaly in three generationsA Collins, M Baraitser, M Pembrey
Journal of Medical Genetics|October 1, 1985
Phenotypic variation in LADD syndromeE Thompson, M Pembrey, J M Graham
Journal of Intellectual Disability Research : JIDR|February 1, 1994
Fragile-X syndrome in North East Essex: towards systematic screening: clinical selectionM Sabaratnam, S Laver, L Butler, et al.
Journal of Intellectual Disability Research : JIDR|March 24, 1999
Diagnosis of fragile-X syndrome: the experiences of parentsB Carmichael, M Pembrey, G Turner, et al.
Archives of Disease in Childhood|March 1, 1981
Sickle cell disease in Saudi Arabs in early childhoodR P Perrine, P John, M Pembrey, et al.
Lancet (London, England)|May 8, 1999
Mitochondrial 16189 variant, thinness at birth, and type-2 diabetes. ALSPAC study team. Avon Longitudinal Study of Pregnancy and ChildhoodK Casteels, K Ong, D Phillips, et al.
Pageof 5