Showing results (11-20 of 3,822) with videos related to
Sort By:
Pageof 383
Journal of Medical Genetics|October 1, 1983
A complex double translocation involving four chromosomes and five breakpoints in a child with mild mental retardationD A Couzin, J L Watt, I A AuchterlonieJournal of Medical Genetics|May 1, 1987
Structural rearrangements in the parents of children with primary trisomy 21D A Couzin, J L Watt, G S StephenCancer Genetics and Cytogenetics|July 1, 1986
A possible case of chronic leukoerythroblastosis associated with t(12;14)(p13;q22) in bone marrow cellsD A Couzin, A A Dawson, G S StephenPrenatal Diagnosis|January 1, 1986
The prenatal detection of a familial pericentric inversion of chromosome 19D A Couzin, J L Watt, G S StephenJournal of Medical Genetics|August 1, 1991
Interstitial deletion of chromosome 13: prognosis and adult phenotypeJ C Dean, S Simpson, D A Couzin, et al.Journal of Medical Genetics|October 1, 1986
Partial trisomy 7 (q32----qter) syndrome in two childrenD A Couzin, N Haites, J L Watt, et al.Prenatal Diagnosis|January 1, 1989
Prenatal diagnosis of a case of 46,XY,18p-/46,XY,18p+ mosaicismG S Stephen, D A Couzin, J L Watt, et al.Journal of Medical Genetics|August 1, 1986
A paracentric inversion of 7q illustrating a possible interchromosomal effectJ L Watt, K Ward, D A Couzin, et al.Journal of Medical Genetics|October 1, 1984
A familial insertion involving an active nucleolar organiser within chromosome 12J L Watt, D A Couzin, D J Lloyd, et al.Journal of Medical Genetics|June 1, 1981
Prenatal detection of Turner's syndrome in conjunction with trisomy 20 mosaicism (45,X/46, X, +0)J L Watt, D A Couzin, A W Johnston, et al.Pageof 383