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Journal of Medical Genetics
|
January 18, 2006
High throughput SNP and expression analyses of candidate genes for non-syndromic oral clefts
J W Park, J Cai, I McIntosh, et al.
Annales De Biologie Clinique
|
March 30, 2004
[A preliminary study to assess the value of the DNA chips SpectralChip to detect subtle constitutional chromosome imbalances]
J-M Lapierre, D Sanlaville, J Kang, et al.
Prenatal Diagnosis
|
June 22, 2000
Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann features
S Fert-Ferrer, A Guichet, J Tantau, et al.
Journal of the American Chemical Society
|
May 19, 2007
Switching from S- to R-selectivity in the Candida antarctica lipase B-catalyzed ring-opening of omega-methylated lactones: tuning polymerizations by ring size
Jeroen van Buijtenen, Bart A C van As, Marloes Verbruggen, et al.
Journal of Medical Genetics
|
May 4, 2004
Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome
L Pinson, J Augé, S Audollent, et al.
European Journal of Human Genetics : EJHG
|
November 28, 2000
PAX2 mutations in renal-coloboma syndrome: mutational hotspot and germline mosaicism
J Amiel, S Audollent, D Joly, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
May 23, 2007
Low mannose-binding lectin concentration is associated with severe infection in patients with hematological cancer who are undergoing chemotherapy
M Vekemans, J Robinson, A Georgala, et al.
Nuclear Medicine and Biology
|
January 27, 2004
Synthesis and evaluation of iodinated TZTP-derivatives as potential radioligands for imaging of muscarinic M2 receptors with SPET
Remco J J Knol, Tamme Doornbos, Jan C van den Bos, et al.
European Journal of Medical Genetics
|
July 9, 2013
Monozygotic twins discordant for 18q21.2qter deletion detected by array CGH in amniotic fluid
M Essaoui, M Nizon, M P Beaujard, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
August 31, 2006
[Preimplantation genetic diagnosis (PGD): results from a Parisian center]
E Feyereisen, S Romana, V Kerbrat, et al.
Page
of 29
Search research articles
Search
Showing results (261-270 of 289) with videos related to
Sort By:
Page
of 29
Journal of Medical Genetics
|
January 18, 2006
High throughput SNP and expression analyses of candidate genes for non-syndromic oral clefts
J W Park, J Cai, I McIntosh, et al.
Annales De Biologie Clinique
|
March 30, 2004
[A preliminary study to assess the value of the DNA chips SpectralChip to detect subtle constitutional chromosome imbalances]
J-M Lapierre, D Sanlaville, J Kang, et al.
Prenatal Diagnosis
|
June 22, 2000
Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann features
S Fert-Ferrer, A Guichet, J Tantau, et al.
Journal of the American Chemical Society
|
May 19, 2007
Switching from S- to R-selectivity in the Candida antarctica lipase B-catalyzed ring-opening of omega-methylated lactones: tuning polymerizations by ring size
Jeroen van Buijtenen, Bart A C van As, Marloes Verbruggen, et al.
Journal of Medical Genetics
|
May 4, 2004
Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome
L Pinson, J Augé, S Audollent, et al.
European Journal of Human Genetics : EJHG
|
November 28, 2000
PAX2 mutations in renal-coloboma syndrome: mutational hotspot and germline mosaicism
J Amiel, S Audollent, D Joly, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
May 23, 2007
Low mannose-binding lectin concentration is associated with severe infection in patients with hematological cancer who are undergoing chemotherapy
M Vekemans, J Robinson, A Georgala, et al.
Nuclear Medicine and Biology
|
January 27, 2004
Synthesis and evaluation of iodinated TZTP-derivatives as potential radioligands for imaging of muscarinic M2 receptors with SPET
Remco J J Knol, Tamme Doornbos, Jan C van den Bos, et al.
European Journal of Medical Genetics
|
July 9, 2013
Monozygotic twins discordant for 18q21.2qter deletion detected by array CGH in amniotic fluid
M Essaoui, M Nizon, M P Beaujard, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
August 31, 2006
[Preimplantation genetic diagnosis (PGD): results from a Parisian center]
E Feyereisen, S Romana, V Kerbrat, et al.
Page
of 29