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Journal of Medical Genetics
|
April 1, 1983
Delineation of trisomy 9 syndrome
D R Romain, J Sullivan
Clinical Genetics
|
January 1, 1992
Fragile site Xq27.3 in a family without mental retardation
D R Romain, C J Chapman
Journal of Medical Genetics
|
July 1, 1991
A rare heteromorphism of chromosome 20 and reproductive loss
D R Romain, S Whyte, D F Callen, et al.
Clinical Genetics
|
September 1, 1979
Discovery of an inherited bisatellited metacentric microchromosome in amniotic cell culture
D R Romain, L Columbano-Green, R H Smythe, et al.
Cancer Genetics and Cytogenetics
|
September 1, 1990
t(2;14)(q23;q32.3) as the sole abnormality in a patient with acute nonlymphocytic leukemia (FAB-M4)
L M Columbano-Green, D R Romain, J Carter, et al.
Journal of Medical Genetics
|
April 1, 1982
Two pericentric inversions, inv(2)(p11q13) and inv(5)(p13q13), in a patient referred for psychiatric problems
D R Romain, C J Chapman, L Columbano-Green, et al.
The New Zealand Medical Journal
|
August 12, 1981
Three unrelated cases of accessory bisatellited microchromosomes in New Zealand
D R Romain, R H Smythe, L M Columbano-Green, et al.
Journal of Medical Genetics
|
July 1, 1992
Trisomy 18 with karyotype 47,XX,-18,+i psu dic(18p)
D R Romain, P Dagger, L M Columbano-Green, et al.
American Journal of Medical Genetics
|
January 11, 1996
Molecular studies of translocations and trisomy involving chromosome 13
W P Robinson, F Bernasconi, F Dutly, et al.
Journal of Medical Genetics
|
September 1, 1990
Partial monosomy for chromosome 22 in a patient with del(22)(pter----q13.1::q13.33----qter)
D R Romain, J Goldsmith, H Cairney, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 24) with videos related to
Sort By:
Page
of 3
Journal of Medical Genetics
|
April 1, 1983
Delineation of trisomy 9 syndrome
D R Romain, J Sullivan
Clinical Genetics
|
January 1, 1992
Fragile site Xq27.3 in a family without mental retardation
D R Romain, C J Chapman
Journal of Medical Genetics
|
July 1, 1991
A rare heteromorphism of chromosome 20 and reproductive loss
D R Romain, S Whyte, D F Callen, et al.
Clinical Genetics
|
September 1, 1979
Discovery of an inherited bisatellited metacentric microchromosome in amniotic cell culture
D R Romain, L Columbano-Green, R H Smythe, et al.
Cancer Genetics and Cytogenetics
|
September 1, 1990
t(2;14)(q23;q32.3) as the sole abnormality in a patient with acute nonlymphocytic leukemia (FAB-M4)
L M Columbano-Green, D R Romain, J Carter, et al.
Journal of Medical Genetics
|
April 1, 1982
Two pericentric inversions, inv(2)(p11q13) and inv(5)(p13q13), in a patient referred for psychiatric problems
D R Romain, C J Chapman, L Columbano-Green, et al.
The New Zealand Medical Journal
|
August 12, 1981
Three unrelated cases of accessory bisatellited microchromosomes in New Zealand
D R Romain, R H Smythe, L M Columbano-Green, et al.
Journal of Medical Genetics
|
July 1, 1992
Trisomy 18 with karyotype 47,XX,-18,+i psu dic(18p)
D R Romain, P Dagger, L M Columbano-Green, et al.
American Journal of Medical Genetics
|
January 11, 1996
Molecular studies of translocations and trisomy involving chromosome 13
W P Robinson, F Bernasconi, F Dutly, et al.
Journal of Medical Genetics
|
September 1, 1990
Partial monosomy for chromosome 22 in a patient with del(22)(pter----q13.1::q13.33----qter)
D R Romain, J Goldsmith, H Cairney, et al.
Page
of 3