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E V Davison

Showing results (21-30 of 39) with videos related to

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British Journal of Haematology|March 1, 1987
Familial myelodysplasia: progressive disease associated with emergency of monosomy 7B Paul, M M Reid, E V Davison, et al.
Journal of Medical Genetics|October 1, 1986
A terminal deletion of the long arm of chromosome 4 [46,XX,del(4)(q33)] in an infant with phenotypic features of Williams syndromeR D Jefferson, J Burn, K L Gaunt, et al.
Journal of Medical Genetics|September 1, 1993
Epidermal mosaicism and Blaschko's linesC Moss, S Larkins, M Stacey, et al.
Cancer Genetics and Cytogenetics|March 1, 1991
Cytogenetic analysis of a congenital fibrosarcomaL R Adam, E V Davison, A J Malcolm, et al.
Prenatal Diagnosis|October 26, 2006
Rapid prenatal diagnosis of common trisomies: discordant results between QF-PCR analysis and karyotype analysis on long-term culture for a case of trisomy 18 detected in CVSS K Allen, A Luharia, C P Gould, et al.
Archives of Disease in Childhood|April 1, 1987
Chromosomes of metastatic retinoblastomaH A Daly, E V Davison, A D Pearson, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 26, 2001
First-trimester prenatal diagnosis of a familial subtelomeric translocationM D Kilby, K J Brackley, J J Walters, et al.
Prenatal Diagnosis|July 5, 2001
Prenatal testing for uniparental disomy (UPD)A M Jay, E Roberts, T Davies, et al.
British Medical Journal|July 1, 1978
Neural tube defects and immunoreactive beta-melanocyte-stimulating hormone in amniotic fluidA G Smith, S Shuster, D Clark, et al.
Prenatal Diagnosis|October 16, 1999
Prenatal diagnosis of mosaicism for partial trisomy 8: a case report including fetal pathologyA Jay, M D Kilby, E Roberts, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
British Journal of Haematology|March 1, 1987
Familial myelodysplasia: progressive disease associated with emergency of monosomy 7B Paul, M M Reid, E V Davison, et al.
Journal of Medical Genetics|October 1, 1986
A terminal deletion of the long arm of chromosome 4 [46,XX,del(4)(q33)] in an infant with phenotypic features of Williams syndromeR D Jefferson, J Burn, K L Gaunt, et al.
Journal of Medical Genetics|September 1, 1993
Epidermal mosaicism and Blaschko's linesC Moss, S Larkins, M Stacey, et al.
Cancer Genetics and Cytogenetics|March 1, 1991
Cytogenetic analysis of a congenital fibrosarcomaL R Adam, E V Davison, A J Malcolm, et al.
Prenatal Diagnosis|October 26, 2006
Rapid prenatal diagnosis of common trisomies: discordant results between QF-PCR analysis and karyotype analysis on long-term culture for a case of trisomy 18 detected in CVSS K Allen, A Luharia, C P Gould, et al.
Archives of Disease in Childhood|April 1, 1987
Chromosomes of metastatic retinoblastomaH A Daly, E V Davison, A D Pearson, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 26, 2001
First-trimester prenatal diagnosis of a familial subtelomeric translocationM D Kilby, K J Brackley, J J Walters, et al.
Prenatal Diagnosis|July 5, 2001
Prenatal testing for uniparental disomy (UPD)A M Jay, E Roberts, T Davies, et al.
British Medical Journal|July 1, 1978
Neural tube defects and immunoreactive beta-melanocyte-stimulating hormone in amniotic fluidA G Smith, S Shuster, D Clark, et al.
Prenatal Diagnosis|October 16, 1999
Prenatal diagnosis of mosaicism for partial trisomy 8: a case report including fetal pathologyA Jay, M D Kilby, E Roberts, et al.
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