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Human Genetics
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June 27, 1978
Silver stain reveals nucleolus organizer regions on a satellited Yq chromosome
W M Howell, P N Howard-Peebles, B M Block, et al.
American Journal of Medical Genetics
|
July 15, 1994
Prenatal diagnosis in known fragile X carriers
A Maddalena, B D Hicks, W C Spence, et al.
The Journal of Pediatrics
|
January 1, 1990
Childhood chronic lymphocytic leukemia with (2;14) translocation
G Yoffe, P N Howard-Peebles, R G Smith, et al.
Human Genetics
|
July 1, 1991
Characterization of seven DA/DAPI-positive bisatellited marker chromosomes by in situ hybridization
R Plattner, N A Heerema, S R Patil, et al.
Journal of Medical Genetics
|
June 1, 1982
A complex chromosome rearrangement resulting in trisomy 15q22 to qter
P N Howard-Peebles, P R Scarbrough, J Sharpe, et al.
The New England Journal of Medicine
|
September 8, 1983
Chromosomal translocation involving the immunoglobulin kappa-chain and heavy-chain loci in a child with chronic lymphocytic leukemia
J A Sonnier, G R Buchanan, P N Howard-Peebles, et al.
Prenatal Diagnosis
|
March 1, 2000
Characterization and clinical implications of marker chromosomes identified at prenatal diagnosis
M M Li, P N Howard-Peebles, L D Killos, et al.
Human Genetics
|
July 1, 1993
Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridization
R Plattner, N A Heerema, P N Howard-Peebles, et al.
Prenatal Diagnosis
|
October 1, 1987
Fetal karyotype following ascertainment of fetal anomalies by ultrasound
C G Palmer, J H Miles, P N Howard-Peebles, et al.
American Journal of Medical Genetics
|
November 24, 1999
Isolated bilateral anophthalmia in a girl with an apparently balanced de novo translocation: 46,XX,t(3;11)(q27;p11.2)
R W Driggers, C J Macri, J Greenwald, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 91) with videos related to
Sort By:
Page
of 10
Human Genetics
|
June 27, 1978
Silver stain reveals nucleolus organizer regions on a satellited Yq chromosome
W M Howell, P N Howard-Peebles, B M Block, et al.
American Journal of Medical Genetics
|
July 15, 1994
Prenatal diagnosis in known fragile X carriers
A Maddalena, B D Hicks, W C Spence, et al.
The Journal of Pediatrics
|
January 1, 1990
Childhood chronic lymphocytic leukemia with (2;14) translocation
G Yoffe, P N Howard-Peebles, R G Smith, et al.
Human Genetics
|
July 1, 1991
Characterization of seven DA/DAPI-positive bisatellited marker chromosomes by in situ hybridization
R Plattner, N A Heerema, S R Patil, et al.
Journal of Medical Genetics
|
June 1, 1982
A complex chromosome rearrangement resulting in trisomy 15q22 to qter
P N Howard-Peebles, P R Scarbrough, J Sharpe, et al.
The New England Journal of Medicine
|
September 8, 1983
Chromosomal translocation involving the immunoglobulin kappa-chain and heavy-chain loci in a child with chronic lymphocytic leukemia
J A Sonnier, G R Buchanan, P N Howard-Peebles, et al.
Prenatal Diagnosis
|
March 1, 2000
Characterization and clinical implications of marker chromosomes identified at prenatal diagnosis
M M Li, P N Howard-Peebles, L D Killos, et al.
Human Genetics
|
July 1, 1993
Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridization
R Plattner, N A Heerema, P N Howard-Peebles, et al.
Prenatal Diagnosis
|
October 1, 1987
Fetal karyotype following ascertainment of fetal anomalies by ultrasound
C G Palmer, J H Miles, P N Howard-Peebles, et al.
American Journal of Medical Genetics
|
November 24, 1999
Isolated bilateral anophthalmia in a girl with an apparently balanced de novo translocation: 46,XX,t(3;11)(q27;p11.2)
R W Driggers, C J Macri, J Greenwald, et al.
Page
of 10