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Molecular and Cellular Probes
|
August 1, 1994
Frequencies of the most common mutations responsible for phenylketonuria in Poland
C Zekanowski, M Nowacka, M Zgulska, et al.
Geburtshilfe Und Frauenheilkunde
|
March 1, 1991
[Prenatal chromosome findings in sonographically conspicuous fetuses]
K Rezai, W Holzgreve, R Schloo, et al.
Prenatal Diagnosis
|
February 1, 1989
A pitfall in the prenatal diagnosis of beta-thalassaemia by RFLP
C Aulehla-Scholz, P Miny, W Holzgreve, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology
|
January 1, 1990
Beta-thalassemia problems in the Turkish population in the F.R.G
W Holzgreve, E Sevinchan, E Kohne, et al.
Clinical Genetics
|
July 1, 1990
Ratio of fetal to maternal DNA is less than 1 in 5000 at different gestational ages in maternal blood
D Gänshirt-Ahlert, M Pohlschmidt, A Gal, et al.
Plant Physiology
|
December 19, 2009
Stimulation of nonselective amino acid export by glutamine dumper proteins
Réjane Pratelli, Lars M Voll, Robin J Horst, et al.
Brain Research
|
May 1, 1989
Natriuretic action of central angiotensin II in conscious rats
T Unger, P J Horst, M Bauer, et al.
International Journal of Andrology
|
September 28, 1998
Prognostic value of male diagnostic profiles in intracytoplasmic sperm injection (ICSI)
B Koppers, P Gassner, D Meschede, et al.
European Journal of Pediatrics
|
May 1, 1981
Heptacarpo-octatarso-dactyly combined with multiple malformation
U Töllner, J Horst, E Manzke, et al.
Genomics
|
October 1, 1991
Aberrant splicing of phenylalanine hydroxylase mRNA: the major cause for phenylketonuria in parts of southern Europe
B Dworniczak, C Aulehla-Scholz, L Kalaydjieva, et al.
Page
of 28
Search research articles
Search
Showing results (161-170 of 278) with videos related to
Sort By:
Page
of 28
Molecular and Cellular Probes
|
August 1, 1994
Frequencies of the most common mutations responsible for phenylketonuria in Poland
C Zekanowski, M Nowacka, M Zgulska, et al.
Geburtshilfe Und Frauenheilkunde
|
March 1, 1991
[Prenatal chromosome findings in sonographically conspicuous fetuses]
K Rezai, W Holzgreve, R Schloo, et al.
Prenatal Diagnosis
|
February 1, 1989
A pitfall in the prenatal diagnosis of beta-thalassaemia by RFLP
C Aulehla-Scholz, P Miny, W Holzgreve, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology
|
January 1, 1990
Beta-thalassemia problems in the Turkish population in the F.R.G
W Holzgreve, E Sevinchan, E Kohne, et al.
Clinical Genetics
|
July 1, 1990
Ratio of fetal to maternal DNA is less than 1 in 5000 at different gestational ages in maternal blood
D Gänshirt-Ahlert, M Pohlschmidt, A Gal, et al.
Plant Physiology
|
December 19, 2009
Stimulation of nonselective amino acid export by glutamine dumper proteins
Réjane Pratelli, Lars M Voll, Robin J Horst, et al.
Brain Research
|
May 1, 1989
Natriuretic action of central angiotensin II in conscious rats
T Unger, P J Horst, M Bauer, et al.
International Journal of Andrology
|
September 28, 1998
Prognostic value of male diagnostic profiles in intracytoplasmic sperm injection (ICSI)
B Koppers, P Gassner, D Meschede, et al.
European Journal of Pediatrics
|
May 1, 1981
Heptacarpo-octatarso-dactyly combined with multiple malformation
U Töllner, J Horst, E Manzke, et al.
Genomics
|
October 1, 1991
Aberrant splicing of phenylalanine hydroxylase mRNA: the major cause for phenylketonuria in parts of southern Europe
B Dworniczak, C Aulehla-Scholz, L Kalaydjieva, et al.
Page
of 28