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Human Genetics
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November 1, 1995
Complement component C3: molecular basis of the C3*S025 variant and evidence for molecular heterogeneity of other variants
T Höhler, M Botto, C Rittner, et al.
Human Genetics
|
November 1, 1995
Influence of transcription and replication on the in situ resolution of immunoglobulin heavy-chain constant region genes: an interphase cytogenetics analysis
M Telhada, C Carvalho, M Carmo-Fonseca, et al.
Human Genetics
|
November 1, 1995
A sublocus of the multicopy microsatellite marker CMS1 maps proximal to spinal muscular atrophy (SMA) as shown by recombinant analysis
G van der Steege, J M Cobben, J Osinga, et al.
Human Genetics
|
December 1, 1995
Detection of chromosome aberrations in paraffin sections of seven gonadal yolk sac tumors of childhood
J Jenderny, E Köster, A Meyer, et al.
Human Genetics
|
December 1, 1995
Parental generalized EEG alpha activity predisposes to spike wave discharges in offspring
H Doose, E Castiglione, S Waltz
Human Genetics
|
December 1, 1995
APC mutation in the alternatively spliced region of exon 9 associated with late onset familial adenomatous polyposis
R B van der Luijt, H F Vasen, C M Tops, et al.
Human Genetics
|
May 1, 1993
FFU complex: an analysis of 491 cases
W Lenz, M Zygulska, J Horst
Human Genetics
|
May 1, 1993
Duplication of the short arm of the X chromosome in mother and daughter
C M Tuck-Muller, J E Martinez, D A Batista, et al.
Human Genetics
|
May 1, 1993
A beta-galactosidase gene mutation identified in both Morquio B disease and infantile GM1 gangliosidosis
Y Suzuki, A Oshima
Human Genetics
|
April 1, 1993
Human reciprocal translocations: is the unbalanced mode at birth predictable?
C Cans, O Cohen, M A Mermet, et al.
Page
of 1,127
Search research articles
Search
Showing results (471-480 of 11,264) with videos related to
Sort By:
Page
of 1,127
Human Genetics
|
November 1, 1995
Complement component C3: molecular basis of the C3*S025 variant and evidence for molecular heterogeneity of other variants
T Höhler, M Botto, C Rittner, et al.
Human Genetics
|
November 1, 1995
Influence of transcription and replication on the in situ resolution of immunoglobulin heavy-chain constant region genes: an interphase cytogenetics analysis
M Telhada, C Carvalho, M Carmo-Fonseca, et al.
Human Genetics
|
November 1, 1995
A sublocus of the multicopy microsatellite marker CMS1 maps proximal to spinal muscular atrophy (SMA) as shown by recombinant analysis
G van der Steege, J M Cobben, J Osinga, et al.
Human Genetics
|
December 1, 1995
Detection of chromosome aberrations in paraffin sections of seven gonadal yolk sac tumors of childhood
J Jenderny, E Köster, A Meyer, et al.
Human Genetics
|
December 1, 1995
Parental generalized EEG alpha activity predisposes to spike wave discharges in offspring
H Doose, E Castiglione, S Waltz
Human Genetics
|
December 1, 1995
APC mutation in the alternatively spliced region of exon 9 associated with late onset familial adenomatous polyposis
R B van der Luijt, H F Vasen, C M Tops, et al.
Human Genetics
|
May 1, 1993
FFU complex: an analysis of 491 cases
W Lenz, M Zygulska, J Horst
Human Genetics
|
May 1, 1993
Duplication of the short arm of the X chromosome in mother and daughter
C M Tuck-Muller, J E Martinez, D A Batista, et al.
Human Genetics
|
May 1, 1993
A beta-galactosidase gene mutation identified in both Morquio B disease and infantile GM1 gangliosidosis
Y Suzuki, A Oshima
Human Genetics
|
April 1, 1993
Human reciprocal translocations: is the unbalanced mode at birth predictable?
C Cans, O Cohen, M A Mermet, et al.
Page
of 1,127