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Genetic Counseling (Geneva, Switzerland)
|
May 3, 2001
De novo unbalanced t(11q;21q) leading to a partial monosomy 21pter-q22.2 and 11q24-qter in a patient initially diagnosed as monosomy 21
M Riegel, A Baumer, A Piram, et al.
Prenatal Diagnosis
|
October 20, 2000
Wolf-Hirschhorn syndrome due to a 3:1 segregation of a maternal balanced t(4;15)(p16.3;q11) translocation
U Zimmermann-Bär, T Stallmach, M Riegel, et al.
Journal of Pediatric Ophthalmology and Strabismus
|
May 1, 1996
Fluorescein angiography and ultrasonography of malignant intraocular medulloepithelioma
J A Shields, R C Eagle, C L Shields, et al.
Pediatric Cardiology
|
October 2, 2007
The fate of children with microdeletion 22q11.2 syndrome and congenital heart defect: clinical course and cardiac outcome
A Kyburz, U Bauersfeld, A Schinzel, et al.
Human Molecular Genetics
|
May 23, 1998
High level of unequal meiotic crossovers at the origin of the 22q11. 2 and 7q11.23 deletions
A Baumer, F Dutly, D Balmer, et al.
Human Mutation
|
June 30, 2000
Isolated central form of tetrahydrobiopterin deficiency associated with hemizygosity on chromosome 11q and a mutant allele of PTPS
N Blau, T Scherer-Oppliger, A Baumer, et al.
Survey of Ophthalmology
|
March 1, 1982
Ocular pathology of Fabry's disease in a hemizygous male following renal transplantation
E M Riegel, K S Pokorny, A H Friedman, et al.
Genetic Counseling (Geneva, Switzerland)
|
November 3, 2004
De novo complex chromosome rearrangement: a study of two patients
D G Melo, J Huber, L R Giuliani, et al.
Journal of Clinical Nursing
|
March 25, 2025
Nurses Must Improve Delirium Care: A Call to Action
V Traynor, B Ho, J Bimrose, et al.
Transplantation
|
February 27, 1996
Tacrolimus (FK506)--its effects on intestinal glucose transport
N L Yanchar, T M Riegel, G Martin, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 48) with videos related to
Sort By:
Page
of 5
Genetic Counseling (Geneva, Switzerland)
|
May 3, 2001
De novo unbalanced t(11q;21q) leading to a partial monosomy 21pter-q22.2 and 11q24-qter in a patient initially diagnosed as monosomy 21
M Riegel, A Baumer, A Piram, et al.
Prenatal Diagnosis
|
October 20, 2000
Wolf-Hirschhorn syndrome due to a 3:1 segregation of a maternal balanced t(4;15)(p16.3;q11) translocation
U Zimmermann-Bär, T Stallmach, M Riegel, et al.
Journal of Pediatric Ophthalmology and Strabismus
|
May 1, 1996
Fluorescein angiography and ultrasonography of malignant intraocular medulloepithelioma
J A Shields, R C Eagle, C L Shields, et al.
Pediatric Cardiology
|
October 2, 2007
The fate of children with microdeletion 22q11.2 syndrome and congenital heart defect: clinical course and cardiac outcome
A Kyburz, U Bauersfeld, A Schinzel, et al.
Human Molecular Genetics
|
May 23, 1998
High level of unequal meiotic crossovers at the origin of the 22q11. 2 and 7q11.23 deletions
A Baumer, F Dutly, D Balmer, et al.
Human Mutation
|
June 30, 2000
Isolated central form of tetrahydrobiopterin deficiency associated with hemizygosity on chromosome 11q and a mutant allele of PTPS
N Blau, T Scherer-Oppliger, A Baumer, et al.
Survey of Ophthalmology
|
March 1, 1982
Ocular pathology of Fabry's disease in a hemizygous male following renal transplantation
E M Riegel, K S Pokorny, A H Friedman, et al.
Genetic Counseling (Geneva, Switzerland)
|
November 3, 2004
De novo complex chromosome rearrangement: a study of two patients
D G Melo, J Huber, L R Giuliani, et al.
Journal of Clinical Nursing
|
March 25, 2025
Nurses Must Improve Delirium Care: A Call to Action
V Traynor, B Ho, J Bimrose, et al.
Transplantation
|
February 27, 1996
Tacrolimus (FK506)--its effects on intestinal glucose transport
N L Yanchar, T M Riegel, G Martin, et al.
Page
of 5