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Human Genetics
|
January 1, 1981
Partial monosomy 7q syndrome due to distal interstitial deletion
R Stallard, R C Juberg
American Journal of Human Genetics
|
May 1, 1981
New deletion syndrome: 1q43
R C Juberg, N R Haney, R Stallard
Clinical Genetics
|
July 1, 1983
Lymphocyte proliferation in a 31-week premature neonate with 69, XXX chromosomal constitution
W B Pittard, R U Sorensen, R Stallard
American Journal of Medical Genetics
|
May 22, 1995
Uniparental isodisomy 13 in a normal female due to transmission of a maternal t(13q13q)
R Stallard, S Krueger, R S James, et al.
Human Genetics
|
January 1, 1983
Dissociation of a t(12;21) resulting in a normal cell line in two trisomic 21 sons of a nonmosaic t(12;21) father?
R C Juberg, R Stallard, P Mowrey, et al.
American Journal of Medical Genetics
|
October 15, 1994
Partial X chromosome trisomy with functional disomy of Xp due to failure of X inactivation
K M Gustashaw, V Zurcher, L H Dickerman, et al.
American Journal of Medical Genetics
|
January 1, 1981
Clinicopathological conference: a newborn monozygotic twin with abnormal facial appearance and respiratory insufficiency
R C Juberg, R Stallard, W J Straughen, et al.
Science (New York, N.Y.)
|
August 12, 1988
Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci
L M Davis, R Stallard, G H Thomas, et al.
Clinical Chemistry
|
September 1, 1992
Noninvasive glucose monitoring in diabetic patients: a preliminary evaluation
M R Robinson, R P Eaton, D M Haaland, et al.
Human Molecular Genetics
|
August 1, 1997
Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNA
T W Depinet, J L Zackowski, W C Earnshaw, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Human Genetics
|
January 1, 1981
Partial monosomy 7q syndrome due to distal interstitial deletion
R Stallard, R C Juberg
American Journal of Human Genetics
|
May 1, 1981
New deletion syndrome: 1q43
R C Juberg, N R Haney, R Stallard
Clinical Genetics
|
July 1, 1983
Lymphocyte proliferation in a 31-week premature neonate with 69, XXX chromosomal constitution
W B Pittard, R U Sorensen, R Stallard
American Journal of Medical Genetics
|
May 22, 1995
Uniparental isodisomy 13 in a normal female due to transmission of a maternal t(13q13q)
R Stallard, S Krueger, R S James, et al.
Human Genetics
|
January 1, 1983
Dissociation of a t(12;21) resulting in a normal cell line in two trisomic 21 sons of a nonmosaic t(12;21) father?
R C Juberg, R Stallard, P Mowrey, et al.
American Journal of Medical Genetics
|
October 15, 1994
Partial X chromosome trisomy with functional disomy of Xp due to failure of X inactivation
K M Gustashaw, V Zurcher, L H Dickerman, et al.
American Journal of Medical Genetics
|
January 1, 1981
Clinicopathological conference: a newborn monozygotic twin with abnormal facial appearance and respiratory insufficiency
R C Juberg, R Stallard, W J Straughen, et al.
Science (New York, N.Y.)
|
August 12, 1988
Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci
L M Davis, R Stallard, G H Thomas, et al.
Clinical Chemistry
|
September 1, 1992
Noninvasive glucose monitoring in diabetic patients: a preliminary evaluation
M R Robinson, R P Eaton, D M Haaland, et al.
Human Molecular Genetics
|
August 1, 1997
Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNA
T W Depinet, J L Zackowski, W C Earnshaw, et al.
Page
of 2