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Clinical Genetics
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November 1, 1986
Diagnostic applications of H-Y serology: H-Y negative phenotype in cells from 45,X/46,XY fetus with testes
E Lieber, S S Wachtel, B Aftalion, et al.
Journal of Perinatal Medicine
|
January 13, 2001
Ellis van Creveld syndrome (chondroectodermal dysplasia, MIM 22550) in three siblings from a non-consanguineous mating
E George, S DeSilva, E Lieber, et al.
Clinical Genetics
|
March 1, 1979
Prenatal diagnosis of trisomy 20 mosaicism
N B Kardon, E Lieber, J G Davis, et al.
The Journal of Pediatrics
|
July 1, 1971
Trisomy 22: a clinical entity
L Y Hsu, L R Shapiro, M Gertner, et al.
American Journal of Medical Genetics. Part A
|
December 12, 2002
Congenital myopathy, recurrent secretory diarrhea, bullous eruption of skin, microcephaly, and deafness: a new genetic syndrome?
J Levy, W Chung, M Garzon, et al.
Clinical Genetics
|
December 1, 1991
De novo 13q partial duplication identified by cytogenetic, biochemical and molecular approaches
S Schwartz, M Harris, R Ehrenpreis, et al.
Transplantation Proceedings
|
August 7, 2016
Early and Long-Term Outcomes of Kidney Grafts Procured From Multiple-Organ Donors and Kidney-Only Donors
H Cholewa, J Chronowska, U Kukla, et al.
Transplantation Proceedings
|
August 7, 2016
Effect of the Second Warm Ischemia Time and Its Components on Early and Long-term Kidney Graft Function
U Kukla, H Cholewa, J Chronowska, et al.
Scientific Reports
|
October 9, 2020
Cooperative rescue of a juvenile capuchin (Cebus imitator) from a Boa constrictor
Katharine M Jack, Michaela R Brown, Margaret S Buehler, et al.
Prenatal Diagnosis
|
July 1, 1992
Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies
L Y Hsu, S Kaffe, E C Jenkins, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 41) with videos related to
Sort By:
Page
of 5
Clinical Genetics
|
November 1, 1986
Diagnostic applications of H-Y serology: H-Y negative phenotype in cells from 45,X/46,XY fetus with testes
E Lieber, S S Wachtel, B Aftalion, et al.
Journal of Perinatal Medicine
|
January 13, 2001
Ellis van Creveld syndrome (chondroectodermal dysplasia, MIM 22550) in three siblings from a non-consanguineous mating
E George, S DeSilva, E Lieber, et al.
Clinical Genetics
|
March 1, 1979
Prenatal diagnosis of trisomy 20 mosaicism
N B Kardon, E Lieber, J G Davis, et al.
The Journal of Pediatrics
|
July 1, 1971
Trisomy 22: a clinical entity
L Y Hsu, L R Shapiro, M Gertner, et al.
American Journal of Medical Genetics. Part A
|
December 12, 2002
Congenital myopathy, recurrent secretory diarrhea, bullous eruption of skin, microcephaly, and deafness: a new genetic syndrome?
J Levy, W Chung, M Garzon, et al.
Clinical Genetics
|
December 1, 1991
De novo 13q partial duplication identified by cytogenetic, biochemical and molecular approaches
S Schwartz, M Harris, R Ehrenpreis, et al.
Transplantation Proceedings
|
August 7, 2016
Early and Long-Term Outcomes of Kidney Grafts Procured From Multiple-Organ Donors and Kidney-Only Donors
H Cholewa, J Chronowska, U Kukla, et al.
Transplantation Proceedings
|
August 7, 2016
Effect of the Second Warm Ischemia Time and Its Components on Early and Long-term Kidney Graft Function
U Kukla, H Cholewa, J Chronowska, et al.
Scientific Reports
|
October 9, 2020
Cooperative rescue of a juvenile capuchin (Cebus imitator) from a Boa constrictor
Katharine M Jack, Michaela R Brown, Margaret S Buehler, et al.
Prenatal Diagnosis
|
July 1, 1992
Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies
L Y Hsu, S Kaffe, E C Jenkins, et al.
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of 5