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K O Simola

Showing results (1-10 of 25) with videos related to

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Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1986
[Current methods of chromosome studies]K O Simola
Clinical Genetics|January 24, 1998
Applicability of a checklist for clinical screening of the fragile X syndromeM Arvio, M Peippo, K O Simola
Clinical Genetics|February 1, 1988
Translocation t(13;14) in nine generations with a case of translocation homozygosityA Eklund, K O Simola, M Ryynänen
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1982
[X-chromosome-linked mental deficiency and the chromosome marker fra(X)(q28)]K O Simola, M Kähkönen, J Leisti
Science (New York, N.Y.)|June 30, 1989
Cloning of breakpoints of a chromosome translocation identifies the AN2 locusM Gessler, K O Simola, G A Bruns
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1997
[Serum screening in risk pregnancies--experiences and attitudes of mothers living in Tampere]R H Nyberg, R Tuimala, K O Simola
Clinical Genetics|November 1, 1992
A case of human chimerism detected by unbalanced chromosomal translocationR H Nyberg, A K Haapala, K O Simola
Clinical Genetics|October 1, 1993
Reply to the letter from Woods and SmithR H Nyberg, A K Haapala, K O Simola
Prenatal Diagnosis|July 1, 1994
The 48,XXYY syndrome: a case detected by maternal serum alpha-fetoprotein screeningR H Nyberg, R Karhu, R Karikoski, et al.
Clinical Dysmorphology|May 13, 1999
A de novo deletion of chromosome 15(q15.2q21.2) in a dysmorphic, mentally retarded child with congenital scalp defectP A Koivisto, H Koivisto, K Haapala, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1986
[Current methods of chromosome studies]K O Simola
Clinical Genetics|January 24, 1998
Applicability of a checklist for clinical screening of the fragile X syndromeM Arvio, M Peippo, K O Simola
Clinical Genetics|February 1, 1988
Translocation t(13;14) in nine generations with a case of translocation homozygosityA Eklund, K O Simola, M Ryynänen
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1982
[X-chromosome-linked mental deficiency and the chromosome marker fra(X)(q28)]K O Simola, M Kähkönen, J Leisti
Science (New York, N.Y.)|June 30, 1989
Cloning of breakpoints of a chromosome translocation identifies the AN2 locusM Gessler, K O Simola, G A Bruns
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1997
[Serum screening in risk pregnancies--experiences and attitudes of mothers living in Tampere]R H Nyberg, R Tuimala, K O Simola
Clinical Genetics|November 1, 1992
A case of human chimerism detected by unbalanced chromosomal translocationR H Nyberg, A K Haapala, K O Simola
Clinical Genetics|October 1, 1993
Reply to the letter from Woods and SmithR H Nyberg, A K Haapala, K O Simola
Prenatal Diagnosis|July 1, 1994
The 48,XXYY syndrome: a case detected by maternal serum alpha-fetoprotein screeningR H Nyberg, R Karhu, R Karikoski, et al.
Clinical Dysmorphology|May 13, 1999
A de novo deletion of chromosome 15(q15.2q21.2) in a dysmorphic, mentally retarded child with congenital scalp defectP A Koivisto, H Koivisto, K Haapala, et al.
Pageof 3