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M J Faed

Showing results (21-30 of 34) with videos related to

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Journal of Medical Genetics|March 1, 1972
Deletion of the long arms of chromosome 18 (46,XX,18q-) associated with absence of IgA and hypothyroidism in an adultM J Faed, R Whyte, C R Paterson, et al.
Archives of Disease in Childhood|December 1, 1985
Wiedemann-Beckwith syndrome in one of monozygotic twinsB Bose, R A Wilkie, M Madlom, et al.
Human Genetics|August 1, 1991
Persistence of two Y chromosomes through meiotic prophase and metaphase I in an XYY manR M Speed, M J Faed, P J Batstone, et al.
Cancer Genetics and Cytogenetics|September 1, 1990
Trisomy 21 in transient myeloproliferative disorderM J Faed, J Robertson, A S Todd, et al.
The British Journal of Dermatology|December 1, 1977
Sister chromatid exchanges in lymphocytes of psoriatics after treatment with 8-methoxypsoralen and long wave ultraviolet radiationD Mourelatos, M J Faed, P W Gould, et al.
Cytogenetics|January 1, 1972
Inherited pericentric inversion of chromosome 5: a family with history of neonatal death and a case of the "cri du chat" syndromeM J Faed, V J Marrian, J Robertson, et al.
Human Genetics|August 15, 2000
Mechanisms of maternal aneuploidy: FISH analysis of oocytes and polar bodies in patients undergoing assisted conceptionR Mahmood, C H Brierley, M J Faed, et al.
The British Journal of Dermatology|September 1, 1980
Sister chromatid exchange and chromosome aberration rates in a group of psoriatics before and after a course of PUVA treatmentM J Faed, L Williamson, S Peterson, et al.
Journal of Medical Genetics|April 1, 1987
Features of di George syndrome in a child with 45,XX,-3,-22,+der(3),t(3;22)(p25;q11)M J Faed, J Robertson, J S Beck, et al.
Journal of Medical Genetics|January 1, 1994
Ascertainment and severity of Marfan syndrome in a Scottish populationJ R Gray, A B Bridges, M J Faed, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Journal of Medical Genetics|March 1, 1972
Deletion of the long arms of chromosome 18 (46,XX,18q-) associated with absence of IgA and hypothyroidism in an adultM J Faed, R Whyte, C R Paterson, et al.
Archives of Disease in Childhood|December 1, 1985
Wiedemann-Beckwith syndrome in one of monozygotic twinsB Bose, R A Wilkie, M Madlom, et al.
Human Genetics|August 1, 1991
Persistence of two Y chromosomes through meiotic prophase and metaphase I in an XYY manR M Speed, M J Faed, P J Batstone, et al.
Cancer Genetics and Cytogenetics|September 1, 1990
Trisomy 21 in transient myeloproliferative disorderM J Faed, J Robertson, A S Todd, et al.
The British Journal of Dermatology|December 1, 1977
Sister chromatid exchanges in lymphocytes of psoriatics after treatment with 8-methoxypsoralen and long wave ultraviolet radiationD Mourelatos, M J Faed, P W Gould, et al.
Cytogenetics|January 1, 1972
Inherited pericentric inversion of chromosome 5: a family with history of neonatal death and a case of the "cri du chat" syndromeM J Faed, V J Marrian, J Robertson, et al.
Human Genetics|August 15, 2000
Mechanisms of maternal aneuploidy: FISH analysis of oocytes and polar bodies in patients undergoing assisted conceptionR Mahmood, C H Brierley, M J Faed, et al.
The British Journal of Dermatology|September 1, 1980
Sister chromatid exchange and chromosome aberration rates in a group of psoriatics before and after a course of PUVA treatmentM J Faed, L Williamson, S Peterson, et al.
Journal of Medical Genetics|April 1, 1987
Features of di George syndrome in a child with 45,XX,-3,-22,+der(3),t(3;22)(p25;q11)M J Faed, J Robertson, J S Beck, et al.
Journal of Medical Genetics|January 1, 1994
Ascertainment and severity of Marfan syndrome in a Scottish populationJ R Gray, A B Bridges, M J Faed, et al.
Pageof 4