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Human Genetics
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January 1, 1983
Terminal or interstitial deletion in chromosome 8 long arm in Langer-Giedion syndrome (TRP II syndrome)?
E M Bühler, U K Bühler, R Christen
Clinical Genetics
|
April 1, 1987
A final word on the tricho-rhino-phalangeal syndromes
E M Bühler, U K Bühler, C Beutler, et al.
Helvetica Paediatrica Acta
|
November 1, 1974
Non-fluorescent Y-chromosome
E M Bühler, U K Bühler, T Tsuchimoto, et al.
Archiv Fur Genetik
|
January 1, 1974
[A rare structural anomaly of the Y chromosome: Y ring (author's transl)]
E M Bühler, T Tsuchimoto, U K Bühler, et al.
Humangenetik
|
January 1, 1975
[45,X/46,SYq dic-Sexchromosome mosaic]
R O Frey, E M Bühler, U K Bühler, et al.
Humangenetik
|
January 1, 1970
Non-condensation of one segment of a chromosome No. 2 in a male with an otherwise normal karyotype (and severe hypospadias)
E M Bühler, U Luchsinger, U K Bühler, et al.
European Journal of Pediatrics
|
March 1, 1980
Chromosome deletion and multiple cartilaginous exostoses
E M Bühler, U K Bühler, G R Stalder, et al.
Helvetica Paediatrica Acta
|
August 1, 1971
[Non-ketotic hyperglycinemia: peracute course in neonatal period]
C Bachmann, M J Mihatsch, R E Baumgartner, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Human Genetics
|
January 1, 1983
Terminal or interstitial deletion in chromosome 8 long arm in Langer-Giedion syndrome (TRP II syndrome)?
E M Bühler, U K Bühler, R Christen
Clinical Genetics
|
April 1, 1987
A final word on the tricho-rhino-phalangeal syndromes
E M Bühler, U K Bühler, C Beutler, et al.
Helvetica Paediatrica Acta
|
November 1, 1974
Non-fluorescent Y-chromosome
E M Bühler, U K Bühler, T Tsuchimoto, et al.
Archiv Fur Genetik
|
January 1, 1974
[A rare structural anomaly of the Y chromosome: Y ring (author's transl)]
E M Bühler, T Tsuchimoto, U K Bühler, et al.
Humangenetik
|
January 1, 1975
[45,X/46,SYq dic-Sexchromosome mosaic]
R O Frey, E M Bühler, U K Bühler, et al.
Humangenetik
|
January 1, 1970
Non-condensation of one segment of a chromosome No. 2 in a male with an otherwise normal karyotype (and severe hypospadias)
E M Bühler, U Luchsinger, U K Bühler, et al.
European Journal of Pediatrics
|
March 1, 1980
Chromosome deletion and multiple cartilaginous exostoses
E M Bühler, U K Bühler, G R Stalder, et al.
Helvetica Paediatrica Acta
|
August 1, 1971
[Non-ketotic hyperglycinemia: peracute course in neonatal period]
C Bachmann, M J Mihatsch, R E Baumgartner, et al.
Page
of 1