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American Journal of Medical Genetics
|
April 15, 2000
Supernumerary chromosome inherited from a maternal balanced translocation leading to pure trisomy 9p
F Tihy, E Lemyre, L Dallaire, et al.
Birth Defects Original Article Series
|
June 1, 1971
Familial holoprosencephaly
L Dallaire, F C Fraser, F W Wiglesworth
Biochimica Et Biophysica Acta
|
September 7, 1982
[Studies on sialidosis and mucolipidosis. Properties of neuraminidase in cultured skin fibroblasts]
G Beauregard, S B Melançon, L Dallaire, et al.
L'Union Medicale Du Canada
|
April 1, 1974
[Comparative study of urine and serum organic acids in newborn infants using gas chromatography]
S B Melançon, B Grignon, L Dallaire, et al.
L'Union Medicale Du Canada
|
November 1, 1971
[Prenatal diagnosis in medical genetics]
L Dallaire, L Pinsky, R A Kinch, et al.
American Journal of Obstetrics and Gynecology
|
November 1, 1990
Screening for trisomy 21 with ultrasonographic determination of biparietal diameter/femur length ratio
G P Marquette, M Boucher, M Desrochers, et al.
Prenatal Diagnosis
|
October 1, 1982
Separation of amniotic fluid cell types in primary culture by Percoll density gradient centrifugation
J Cousineau, M Potier, L Dallaire, et al.
The Journal of Obstetrics and Gynaecology of the British Commonwealth
|
October 1, 1974
Feto-maternal amino acid metabolism
L Dallaire, M Potier, S B Melancon, et al.
Prenatal Diagnosis
|
November 1, 1992
Prenatal identification of a 45,X/46,Xder(Y) mosaicism and confirmation by high resolution cytogenetics and fluorescence in situ hybridization
J Qu, L Dallaire, R Fetni, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 2, 1977
N-Acetyl-beta-hexosaminidase isoenzymes of amniotic fluid and maternal serum. Their relevance to prenatal diagnosis of the GM2 gangliosidoses
M Potier, G Boire, L Dallaire, et al.
Page
of 13
Search research articles
Search
Showing results (31-40 of 121) with videos related to
Sort By:
Page
of 13
American Journal of Medical Genetics
|
April 15, 2000
Supernumerary chromosome inherited from a maternal balanced translocation leading to pure trisomy 9p
F Tihy, E Lemyre, L Dallaire, et al.
Birth Defects Original Article Series
|
June 1, 1971
Familial holoprosencephaly
L Dallaire, F C Fraser, F W Wiglesworth
Biochimica Et Biophysica Acta
|
September 7, 1982
[Studies on sialidosis and mucolipidosis. Properties of neuraminidase in cultured skin fibroblasts]
G Beauregard, S B Melançon, L Dallaire, et al.
L'Union Medicale Du Canada
|
April 1, 1974
[Comparative study of urine and serum organic acids in newborn infants using gas chromatography]
S B Melançon, B Grignon, L Dallaire, et al.
L'Union Medicale Du Canada
|
November 1, 1971
[Prenatal diagnosis in medical genetics]
L Dallaire, L Pinsky, R A Kinch, et al.
American Journal of Obstetrics and Gynecology
|
November 1, 1990
Screening for trisomy 21 with ultrasonographic determination of biparietal diameter/femur length ratio
G P Marquette, M Boucher, M Desrochers, et al.
Prenatal Diagnosis
|
October 1, 1982
Separation of amniotic fluid cell types in primary culture by Percoll density gradient centrifugation
J Cousineau, M Potier, L Dallaire, et al.
The Journal of Obstetrics and Gynaecology of the British Commonwealth
|
October 1, 1974
Feto-maternal amino acid metabolism
L Dallaire, M Potier, S B Melancon, et al.
Prenatal Diagnosis
|
November 1, 1992
Prenatal identification of a 45,X/46,Xder(Y) mosaicism and confirmation by high resolution cytogenetics and fluorescence in situ hybridization
J Qu, L Dallaire, R Fetni, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 2, 1977
N-Acetyl-beta-hexosaminidase isoenzymes of amniotic fluid and maternal serum. Their relevance to prenatal diagnosis of the GM2 gangliosidoses
M Potier, G Boire, L Dallaire, et al.
Page
of 13