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M E Pembrey

Showing results (31-40 of 99) with videos related to

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Lancet (London, England)|June 16, 1973
Maternal synthesis of haemoglobin F in pregnancyM E Pembrey, D J Weatherall, J B Clegg
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Inheritance of parental chromosomes 15 in Angelman syndrome--implications for the familyT Webb, S Malcolm, M E Pembrey, et al.
Journal of Medical Genetics|January 1, 1988
Service experience using DNA analysis for genetic prediction in Duchenne muscular dystrophyJ Goodship, S Malcolm, M E Robertson, et al.
Journal of Medical Genetics|June 1, 1995
A clinical and genetic study of campomelic dysplasiaS Mansour, C M Hall, M E Pembrey, et al.
Journal of Medical Genetics|April 1, 1987
A girl with the Weaver syndromeE M Thompson, S Hill, J V Leonard, et al.
Lancet (London, England)|October 6, 1990
Multicentre study of antenatal calyceal dilatation detected by ultrasoundL S Chittty, M E Pembrey, P M Chudleigh, et al.
Clinical Genetics|December 1, 1989
Phenotypical features of an unique Irish family with severe autosomal recessive Osteogenesis imperfectaE M Thompson, I D Young, C M Hall, et al.
Annals of Internal Medicine|January 1, 1978
Natural history of sickle cell anemia in Saudi Arabs. A study of 270 subjectsR P Perrine, M E Pembrey, P John, et al.
Journal of Medical Genetics|July 1, 1987
Osteogenesis imperfecta type IIA: evidence for dominant inheritanceI D Young, E M Thompson, C M Hall, et al.
Journal of Medical Genetics|July 1, 1987
Recurrence risks and prognosis in severe sporadic osteogenesis imperfectaE M Thompson, I D Young, C M Hall, et al.
Pageof 10

Showing results (31-40 of 99) with videos related to

Sort By:
Pageof 10
Lancet (London, England)|June 16, 1973
Maternal synthesis of haemoglobin F in pregnancyM E Pembrey, D J Weatherall, J B Clegg
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Inheritance of parental chromosomes 15 in Angelman syndrome--implications for the familyT Webb, S Malcolm, M E Pembrey, et al.
Journal of Medical Genetics|January 1, 1988
Service experience using DNA analysis for genetic prediction in Duchenne muscular dystrophyJ Goodship, S Malcolm, M E Robertson, et al.
Journal of Medical Genetics|June 1, 1995
A clinical and genetic study of campomelic dysplasiaS Mansour, C M Hall, M E Pembrey, et al.
Journal of Medical Genetics|April 1, 1987
A girl with the Weaver syndromeE M Thompson, S Hill, J V Leonard, et al.
Lancet (London, England)|October 6, 1990
Multicentre study of antenatal calyceal dilatation detected by ultrasoundL S Chittty, M E Pembrey, P M Chudleigh, et al.
Clinical Genetics|December 1, 1989
Phenotypical features of an unique Irish family with severe autosomal recessive Osteogenesis imperfectaE M Thompson, I D Young, C M Hall, et al.
Annals of Internal Medicine|January 1, 1978
Natural history of sickle cell anemia in Saudi Arabs. A study of 270 subjectsR P Perrine, M E Pembrey, P John, et al.
Journal of Medical Genetics|July 1, 1987
Osteogenesis imperfecta type IIA: evidence for dominant inheritanceI D Young, E M Thompson, C M Hall, et al.
Journal of Medical Genetics|July 1, 1987
Recurrence risks and prognosis in severe sporadic osteogenesis imperfectaE M Thompson, I D Young, C M Hall, et al.
Pageof 10