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Hormone Research
|
January 1, 1988
46XY siblings with inadequate virilization and CNS deficiency
R P Hoffman, M W Steele, P A Lee, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 15, 1991
X/Y translocations resulting from recombination between homologous sequences on Xp and Yq
P H Yen, S P Tsai, S L Wenger, et al.
Cancer Genetics and Cytogenetics
|
April 1, 1988
Rhabdomyosarcoma in Roberts syndrome
S L Wenger, J Blatt, M W Steele, et al.
American Journal of Medical Genetics
|
February 15, 1994
Three unrelated cases of paracentric inversions of 1p in individuals with abnormal phenotypes
A M Estop, V Bansal, A Lin, et al.
American Journal of Medical Genetics
|
November 1, 1988
Interstitial and terminal deletions of the long arm of chromosome 4: further delineation of phenotypes
A E Lin, K L Garver, G Diggans, et al.
American Journal of Medical Genetics
|
November 6, 1995
Infundibulopelvic stenosis, multicystic kidney, and calyectasis in a kindred: clinical observations and genetic analysis
M Kobayashi, B S Kaplan, R D Bellah, et al.
Human Genetics
|
January 28, 1999
Relaxation of imprinting in Prader-Willi syndrome
P K Rogan, J R Seip, L M White, et al.
Human Genetics
|
July 1, 1996
A molecular anatomical analysis of mosaic trisomy 16
J M Greally, K Neiswanger, J H Cummins, et al.
Page
of 7
Search research articles
Search
Showing results (61-70 of 68) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 68 results.
Hormone Research
|
January 1, 1988
46XY siblings with inadequate virilization and CNS deficiency
R P Hoffman, M W Steele, P A Lee, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 15, 1991
X/Y translocations resulting from recombination between homologous sequences on Xp and Yq
P H Yen, S P Tsai, S L Wenger, et al.
Cancer Genetics and Cytogenetics
|
April 1, 1988
Rhabdomyosarcoma in Roberts syndrome
S L Wenger, J Blatt, M W Steele, et al.
American Journal of Medical Genetics
|
February 15, 1994
Three unrelated cases of paracentric inversions of 1p in individuals with abnormal phenotypes
A M Estop, V Bansal, A Lin, et al.
American Journal of Medical Genetics
|
November 1, 1988
Interstitial and terminal deletions of the long arm of chromosome 4: further delineation of phenotypes
A E Lin, K L Garver, G Diggans, et al.
American Journal of Medical Genetics
|
November 6, 1995
Infundibulopelvic stenosis, multicystic kidney, and calyectasis in a kindred: clinical observations and genetic analysis
M Kobayashi, B S Kaplan, R D Bellah, et al.
Human Genetics
|
January 28, 1999
Relaxation of imprinting in Prader-Willi syndrome
P K Rogan, J R Seip, L M White, et al.
Human Genetics
|
July 1, 1996
A molecular anatomical analysis of mosaic trisomy 16
J M Greally, K Neiswanger, J H Cummins, et al.
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of 7