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Organic & Biomolecular Chemistry
|
March 19, 2010
Microwave-induced electrostatic etching: generation of highly reactive magnesium for application in Grignard reagent formation
Bastiaan H P van de Kruijs, Mark H C L Dressen, Jan Meuldijk, et al.
Genes, Chromosomes & Cancer
|
March 10, 2001
Reassessment of childhood B-lineage lymphoblastic leukemia karyotypes using spectral analysis
H Elghezal, G Le Guyader, I Radford-Weiss, et al.
Prenatal Diagnosis
|
September 24, 2004
Prenatal diagnosis and characterization of an analphoid marker chromosome 16
A C Tabet, P Gosset, H Elghezal, et al.
Biochemical and Biophysical Research Communications
|
June 6, 2006
Acyl-CoA dehydrogenase 9 (ACAD 9) is the long-chain acyl-CoA dehydrogenase in human embryonic and fetal brain
N A Oey, J P N Ruiter, L Ijlst, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
April 23, 2019
Cost-effectiveness of five prenatal screening strategies for trisomies and other unbalanced chromosomal abnormalities: model-based analysis
A Le Bras, L J Salomon, L Bussières, et al.
Journal of Medical Genetics
|
April 5, 2003
Cryptic terminal deletion of chromosome 9q34: a novel cause of syndromic obesity in childhood?
V Cormier-Daire, F Molinari, M Rio, et al.
Clinical Genetics
|
July 3, 1998
Wilms' tumor and gonadal dysgenesis in a child with the 2q37.1 deletion syndrome
G Viot-Szoboszlai, J Amiel, F Doz, et al.
American Journal of Medical Genetics
|
November 29, 2002
Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature
S Brisset, G Joly, C Ozilou, et al.
Lancet (London, England)
|
January 22, 1994
SRY-negative XX fetus with complete male phenotype
E Vilain, B Le Fiblec, N Morichon-Delvallez, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
September 13, 2005
[Microarray CGH: principle and use for constitutional disorders]
D Sanlaville, J M Lapierre, A Coquin, et al.
Page
of 29
Search research articles
Search
Showing results (201-210 of 289) with videos related to
Sort By:
Page
of 29
Organic & Biomolecular Chemistry
|
March 19, 2010
Microwave-induced electrostatic etching: generation of highly reactive magnesium for application in Grignard reagent formation
Bastiaan H P van de Kruijs, Mark H C L Dressen, Jan Meuldijk, et al.
Genes, Chromosomes & Cancer
|
March 10, 2001
Reassessment of childhood B-lineage lymphoblastic leukemia karyotypes using spectral analysis
H Elghezal, G Le Guyader, I Radford-Weiss, et al.
Prenatal Diagnosis
|
September 24, 2004
Prenatal diagnosis and characterization of an analphoid marker chromosome 16
A C Tabet, P Gosset, H Elghezal, et al.
Biochemical and Biophysical Research Communications
|
June 6, 2006
Acyl-CoA dehydrogenase 9 (ACAD 9) is the long-chain acyl-CoA dehydrogenase in human embryonic and fetal brain
N A Oey, J P N Ruiter, L Ijlst, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
April 23, 2019
Cost-effectiveness of five prenatal screening strategies for trisomies and other unbalanced chromosomal abnormalities: model-based analysis
A Le Bras, L J Salomon, L Bussières, et al.
Journal of Medical Genetics
|
April 5, 2003
Cryptic terminal deletion of chromosome 9q34: a novel cause of syndromic obesity in childhood?
V Cormier-Daire, F Molinari, M Rio, et al.
Clinical Genetics
|
July 3, 1998
Wilms' tumor and gonadal dysgenesis in a child with the 2q37.1 deletion syndrome
G Viot-Szoboszlai, J Amiel, F Doz, et al.
American Journal of Medical Genetics
|
November 29, 2002
Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature
S Brisset, G Joly, C Ozilou, et al.
Lancet (London, England)
|
January 22, 1994
SRY-negative XX fetus with complete male phenotype
E Vilain, B Le Fiblec, N Morichon-Delvallez, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
September 13, 2005
[Microarray CGH: principle and use for constitutional disorders]
D Sanlaville, J M Lapierre, A Coquin, et al.
Page
of 29