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M C Addor

Showing results (11-20 of 35) with videos related to

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Journal De Genetique Humaine|August 1, 1986
[Hereditary multicentric osteolysis]M C Addor, G Pescia, D Egloff, et al.
Genetic Counseling (Geneva, Switzerland)|July 14, 2000
An uncommon G375C substitution in a newborn with achondroplasiaM C Addor, F Gudinchet, A Truttmann, et al.
Journal De Genetique Humaine|June 1, 1984
[Familial study of vesico-ureteral reflux]M C Addor, G Pescia, J P Guignard, et al.
Genetic Counseling (Geneva, Switzerland)|February 1, 2003
Partial trisomy 20q in a newborn with dextrocardiaM C Addor, C Castagne, J L Micheli, et al.
European Journal of Pediatrics|March 29, 2001
A characteristic EEG pattern in 4p-syndrome: case report and review of the literatureA Zankl, M C Addor, M M Maeder-Ingvar, et al.
Genetic Counseling (Geneva, Switzerland)|February 1, 2003
Two brothers with atypical syndactylies, cerebellar atrophy and severe mental retardationD F Schorderet, M C Addor, Ph Maeder, et al.
Revue Medicale De La Suisse Romande|July 27, 2000
[Fluorescent in situ hybridization (FISH). Diagnostic aide in certain chromosomal anomalies]A Zankl, M C Addor, F Thonney, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
A new case of Pfeiffer syndrome with mutation in FGFR2M C Addor, F Gudinchet, R N Laurini, et al.
Revue Medicale De La Suisse Romande|April 1, 1993
[Alpha-fetoprotein and chromosome aberrations: what else? Results of a prospective study concerning 15,533 pregnancies]P Marguerat, D Weihs, G Pescia, et al.
European Journal of Pediatrics|June 5, 2001
Fatal outcome in a female monozygotic twin with X-linked hypohydrotic ectodermal dysplasia (XLHED) due to a de novo t(X;9) translocation with probable disruption of the EDA geneA Zankl, M C Addor, P Cousin, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
Journal De Genetique Humaine|August 1, 1986
[Hereditary multicentric osteolysis]M C Addor, G Pescia, D Egloff, et al.
Genetic Counseling (Geneva, Switzerland)|July 14, 2000
An uncommon G375C substitution in a newborn with achondroplasiaM C Addor, F Gudinchet, A Truttmann, et al.
Journal De Genetique Humaine|June 1, 1984
[Familial study of vesico-ureteral reflux]M C Addor, G Pescia, J P Guignard, et al.
Genetic Counseling (Geneva, Switzerland)|February 1, 2003
Partial trisomy 20q in a newborn with dextrocardiaM C Addor, C Castagne, J L Micheli, et al.
European Journal of Pediatrics|March 29, 2001
A characteristic EEG pattern in 4p-syndrome: case report and review of the literatureA Zankl, M C Addor, M M Maeder-Ingvar, et al.
Genetic Counseling (Geneva, Switzerland)|February 1, 2003
Two brothers with atypical syndactylies, cerebellar atrophy and severe mental retardationD F Schorderet, M C Addor, Ph Maeder, et al.
Revue Medicale De La Suisse Romande|July 27, 2000
[Fluorescent in situ hybridization (FISH). Diagnostic aide in certain chromosomal anomalies]A Zankl, M C Addor, F Thonney, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
A new case of Pfeiffer syndrome with mutation in FGFR2M C Addor, F Gudinchet, R N Laurini, et al.
Revue Medicale De La Suisse Romande|April 1, 1993
[Alpha-fetoprotein and chromosome aberrations: what else? Results of a prospective study concerning 15,533 pregnancies]P Marguerat, D Weihs, G Pescia, et al.
European Journal of Pediatrics|June 5, 2001
Fatal outcome in a female monozygotic twin with X-linked hypohydrotic ectodermal dysplasia (XLHED) due to a de novo t(X;9) translocation with probable disruption of the EDA geneA Zankl, M C Addor, P Cousin, et al.
Pageof 4