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American Journal of Medical Genetics
|
May 15, 1993
Molecular and cytogenetic characterization of 9p- abnormalities
A S Teebi, L Gibson, J McGrath, et al.
The New England Journal of Medicine
|
November 20, 1975
Expression of H-Y antigen in human males with two Y chromosomes
S S Wachtel, G C Koo, W R Breg, et al.
American Journal of Medical Genetics
|
February 1, 1991
Anthropometric comparison of mentally retarded males with and without the fragile X syndrome
M G Butler, G A Allen, J L Haynes, et al.
Prenatal Diagnosis
|
January 1, 1993
Fetal blood sampling and cytogenetic abnormalities
J D Liou, C P Chen, W R Breg, et al.
Prenatal Diagnosis
|
February 1, 1996
Prenatal detection of two different monosomic cell lines by chorionic villus sampling
T Y Hsu, J D Liou, J A Copel, et al.
Clinical Genetics
|
October 1, 1977
7q deletion syndrome (7q32 leads to 7qter)
E L Harris, R S Wappner, C G Palmer, et al.
Clinical Genetics
|
December 1, 1979
Complete and partial trisomy of different segments of chromosome 8: case reports and review
R M Fineman, R C Ablow, W R Breg, et al.
The New England Journal of Medicine
|
May 31, 1984
Fragile X in a survey of 75 autistic males
M S Watson, J F Leckman, B Annex, et al.
American Journal of Medical Genetics
|
May 1, 1988
Aneuploidy and the fragile X syndrome
M S Watson, W R Breg, D Pauls, et al.
The New England Journal of Medicine
|
October 6, 1983
Fetal cystic hygroma. Cause and natural history
F A Chervenak, G Isaacson, K J Blakemore, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 87) with videos related to
Sort By:
Page
of 9
American Journal of Medical Genetics
|
May 15, 1993
Molecular and cytogenetic characterization of 9p- abnormalities
A S Teebi, L Gibson, J McGrath, et al.
The New England Journal of Medicine
|
November 20, 1975
Expression of H-Y antigen in human males with two Y chromosomes
S S Wachtel, G C Koo, W R Breg, et al.
American Journal of Medical Genetics
|
February 1, 1991
Anthropometric comparison of mentally retarded males with and without the fragile X syndrome
M G Butler, G A Allen, J L Haynes, et al.
Prenatal Diagnosis
|
January 1, 1993
Fetal blood sampling and cytogenetic abnormalities
J D Liou, C P Chen, W R Breg, et al.
Prenatal Diagnosis
|
February 1, 1996
Prenatal detection of two different monosomic cell lines by chorionic villus sampling
T Y Hsu, J D Liou, J A Copel, et al.
Clinical Genetics
|
October 1, 1977
7q deletion syndrome (7q32 leads to 7qter)
E L Harris, R S Wappner, C G Palmer, et al.
Clinical Genetics
|
December 1, 1979
Complete and partial trisomy of different segments of chromosome 8: case reports and review
R M Fineman, R C Ablow, W R Breg, et al.
The New England Journal of Medicine
|
May 31, 1984
Fragile X in a survey of 75 autistic males
M S Watson, J F Leckman, B Annex, et al.
American Journal of Medical Genetics
|
May 1, 1988
Aneuploidy and the fragile X syndrome
M S Watson, W R Breg, D Pauls, et al.
The New England Journal of Medicine
|
October 6, 1983
Fetal cystic hygroma. Cause and natural history
F A Chervenak, G Isaacson, K J Blakemore, et al.
Page
of 9