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Human Genetics
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January 1, 1985
Evidence against close linkage of the loci for fraXq of Martin-Bell syndrome and for factor IX
B Zoll, J Arnemann, M Krawczak, et al.
Prenatal Diagnosis
|
July 2, 2004
Maternal serum levels of placental proteins after in vitro fertilisation and their implications for prenatal screening
N A Bersinger, D Wunder, F Vanderlick, et al.
Human Genetics
|
November 1, 1994
Putative non-Mendelian transmission of retinoblastoma in males: a phenotypic segregation analysis of 150 pedigrees
F L Munier, L Arabien, P Flodman, et al.
Revue Medicale De La Suisse Romande
|
October 1, 1994
[Defects in neural tube closure in the Vaud canton 1980-1992. The impact of prenatal diagnosis]
P Marguerat, M C Addor, G Pescia, et al.
Annales De Genetique
|
January 1, 1988
Cytogenetic analysis of 570 first trimester chorionic villi samplings: technique and results
M Jotterand-Bellomo, G Pescia, H Nguyen The, et al.
Human Genetics
|
July 1, 1992
Paternal selection favoring mutant alleles of the retinoblastoma susceptibility gene
F Munier, M A Spence, G Pescia, et al.
American Journal of Human Genetics
|
December 5, 1998
Evidence of somatic and germinal mosaicism in pseudo-low-penetrant hereditary retinoblastoma, by constitutional and single-sperm mutation analysis
F L Munier, F Thonney, A Girardet, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1996
Delineation of a 1-cM region on distal 5q containing the locus for corneal dystrophies Groenouw type I and lattice type I and exclusion of the candidate genes SPARC and LOX
E Korvatska, F L Munier, L Zografos, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
November 1, 1993
Pseudo low penetrance in retinoblastoma. Fortuitous familial aggregation of sporadic cases caused by independently derived mutations in two large pedigrees
F L Munier, M X Wang, M A Spence, et al.
Revue Medicale De La Suisse Romande
|
December 1, 1994
[Prenatal diagnosis of genetic diseases: Lausanne experience 1989-1993]
S Fokstuen, G Pescia, M C Addor, et al.
Page
of 12
Search research articles
Search
Showing results (101-110 of 117) with videos related to
Sort By:
Page
of 12
Human Genetics
|
January 1, 1985
Evidence against close linkage of the loci for fraXq of Martin-Bell syndrome and for factor IX
B Zoll, J Arnemann, M Krawczak, et al.
Prenatal Diagnosis
|
July 2, 2004
Maternal serum levels of placental proteins after in vitro fertilisation and their implications for prenatal screening
N A Bersinger, D Wunder, F Vanderlick, et al.
Human Genetics
|
November 1, 1994
Putative non-Mendelian transmission of retinoblastoma in males: a phenotypic segregation analysis of 150 pedigrees
F L Munier, L Arabien, P Flodman, et al.
Revue Medicale De La Suisse Romande
|
October 1, 1994
[Defects in neural tube closure in the Vaud canton 1980-1992. The impact of prenatal diagnosis]
P Marguerat, M C Addor, G Pescia, et al.
Annales De Genetique
|
January 1, 1988
Cytogenetic analysis of 570 first trimester chorionic villi samplings: technique and results
M Jotterand-Bellomo, G Pescia, H Nguyen The, et al.
Human Genetics
|
July 1, 1992
Paternal selection favoring mutant alleles of the retinoblastoma susceptibility gene
F Munier, M A Spence, G Pescia, et al.
American Journal of Human Genetics
|
December 5, 1998
Evidence of somatic and germinal mosaicism in pseudo-low-penetrant hereditary retinoblastoma, by constitutional and single-sperm mutation analysis
F L Munier, F Thonney, A Girardet, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1996
Delineation of a 1-cM region on distal 5q containing the locus for corneal dystrophies Groenouw type I and lattice type I and exclusion of the candidate genes SPARC and LOX
E Korvatska, F L Munier, L Zografos, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
November 1, 1993
Pseudo low penetrance in retinoblastoma. Fortuitous familial aggregation of sporadic cases caused by independently derived mutations in two large pedigrees
F L Munier, M X Wang, M A Spence, et al.
Revue Medicale De La Suisse Romande
|
December 1, 1994
[Prenatal diagnosis of genetic diseases: Lausanne experience 1989-1993]
S Fokstuen, G Pescia, M C Addor, et al.
Page
of 12