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H Zierler

Showing results (11-20 of 24) with videos related to

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Wiener Medizinische Wochenschrift (1946)|April 15, 1979
[Prenatal diagnosis of trisomy-18-fetus of two women with chromosomal aberrations (author's transl)]H Zierler, W Rosenkranz, R Winter, et al.
Padiatrie Und Padologie|January 1, 1981
[Asymmetric mixed gonadal dysgenesis (author's transl)]J Glatzl, W Müller, H Zierler, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|February 1, 1991
[Holoprosencephaly: criteria and consequences for prenatal diagnosis]K Hecher, H Zierler, R Spernol, et al.
Wiener Klinische Wochenschrift|January 1, 1996
[Pregnancy termination after prenatal diagnosis--data of the Styrian malformation register (1985-1992)]M C Häusler, A Berghold, H Zierler, et al.
Wiener Klinische Wochenschrift|September 26, 1986
[Type and incidence of abnormalities in 23,939 newborn infants in a 5-year period]K Rosanelli, H Rosegger, H L Zeichen, et al.
Gynakologisch-Geburtshilfliche Rundschau|January 1, 1996
[The triple test scenario for Styria. With data of the Styria Abnormalities Register]M C Häusler, A Berghold, H Zierler, et al.
American Journal of Medical Genetics|December 26, 2001
Clinical and molecular cytogenetic characterization of two patients with partial trisomy 1q41-qter: further delineation of partial trisomy 1q syndromeW Emberger, E Petek, P M Kroisel, et al.
Geburtshilfe Und Frauenheilkunde|May 1, 1992
[Doppler ultrasound of the umbilical artery in fetuses with sonographically abnormal findings and/or chromosome abnormalities (corrected)]K Hecher, R Spernol, D Wimmer-Hebein, et al.
American Journal of Medical Genetics|May 20, 1999
Mosaicism in a fragile X male including a de novo deletion in the FMR1 geneE Petek, P M Kroisel, M Schuster, et al.
Prenatal Diagnosis|January 1, 1985
Prenatal diagnosis of campomelic dysplasia by ultrasonographyR Winter, W Rosenkranz, H Hofmann, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Wiener Medizinische Wochenschrift (1946)|April 15, 1979
[Prenatal diagnosis of trisomy-18-fetus of two women with chromosomal aberrations (author's transl)]H Zierler, W Rosenkranz, R Winter, et al.
Padiatrie Und Padologie|January 1, 1981
[Asymmetric mixed gonadal dysgenesis (author's transl)]J Glatzl, W Müller, H Zierler, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|February 1, 1991
[Holoprosencephaly: criteria and consequences for prenatal diagnosis]K Hecher, H Zierler, R Spernol, et al.
Wiener Klinische Wochenschrift|January 1, 1996
[Pregnancy termination after prenatal diagnosis--data of the Styrian malformation register (1985-1992)]M C Häusler, A Berghold, H Zierler, et al.
Wiener Klinische Wochenschrift|September 26, 1986
[Type and incidence of abnormalities in 23,939 newborn infants in a 5-year period]K Rosanelli, H Rosegger, H L Zeichen, et al.
Gynakologisch-Geburtshilfliche Rundschau|January 1, 1996
[The triple test scenario for Styria. With data of the Styria Abnormalities Register]M C Häusler, A Berghold, H Zierler, et al.
American Journal of Medical Genetics|December 26, 2001
Clinical and molecular cytogenetic characterization of two patients with partial trisomy 1q41-qter: further delineation of partial trisomy 1q syndromeW Emberger, E Petek, P M Kroisel, et al.
Geburtshilfe Und Frauenheilkunde|May 1, 1992
[Doppler ultrasound of the umbilical artery in fetuses with sonographically abnormal findings and/or chromosome abnormalities (corrected)]K Hecher, R Spernol, D Wimmer-Hebein, et al.
American Journal of Medical Genetics|May 20, 1999
Mosaicism in a fragile X male including a de novo deletion in the FMR1 geneE Petek, P M Kroisel, M Schuster, et al.
Prenatal Diagnosis|January 1, 1985
Prenatal diagnosis of campomelic dysplasia by ultrasonographyR Winter, W Rosenkranz, H Hofmann, et al.
Pageof 3