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A A Schinzel

Showing results (1-10 of 37) with videos related to

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Progress in Medical Genetics|January 1, 1983
Cardiovascular defects associated with chromosomal aberrations and malformation syndromesA A Schinzel
American Journal of Human Genetics|February 1, 1991
Uniparental disomy and gene localizationA A Schinzel
Ergebnisse Der Inneren Medizin Und Kinderheilkunde|January 1, 1993
[Etiology of numerical and structural aberrations of the X chromosome. A study with highly polymorphic DNA markers]I Lorda-Sanchez, A A Schinzel
Human Genetics|March 1, 1993
Deletion breakpoints associated with the Prader-Willi and Angelman syndromes (15q11-q13) are not sites of high homologous recombinationW P Robinson, R Spiegel, A A Schinzel
The Journal of Pediatrics|December 1, 1979
Monozygotic twinning and structural defectsA A Schinzel, D W Smith, J R Miller
Clinical Dysmorphology|January 1, 1994
An interstitial deletion of proximal 8q (q11-q13) in a girl with Silver-Russell syndrome-like featuresA A Schinzel, W P Robinson, F Binkert, et al.
Journal of Medical Genetics|May 1, 1994
Multiple origins of X chromosome tetrasomyW P Robinson, F Binkert, A A Schinzel, et al.
Journal of Medical Genetics|April 1, 1996
The dysmorphic human-mouse homology database (DHMHD): an interactive World-Wide Web resource for gene mappingC D Evans, A G Searle, A A Schinzel, et al.
Human Genetics|July 1, 1992
Reduced recombination and paternal age effect in Klinefelter syndromeI Lorda-Sanchez, F Binkert, M Maechler, et al.
American Journal of Human Genetics|February 1, 1992
No evidence for a paternal interchromosomal effect from analysis of the origin of nondisjunction in Down syndrome patients with concomitant familial chromosome rearrangementsA A Schinzel, P A Adelsberger, F Binkert, et al.
Pageof 4

Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
Progress in Medical Genetics|January 1, 1983
Cardiovascular defects associated with chromosomal aberrations and malformation syndromesA A Schinzel
American Journal of Human Genetics|February 1, 1991
Uniparental disomy and gene localizationA A Schinzel
Ergebnisse Der Inneren Medizin Und Kinderheilkunde|January 1, 1993
[Etiology of numerical and structural aberrations of the X chromosome. A study with highly polymorphic DNA markers]I Lorda-Sanchez, A A Schinzel
Human Genetics|March 1, 1993
Deletion breakpoints associated with the Prader-Willi and Angelman syndromes (15q11-q13) are not sites of high homologous recombinationW P Robinson, R Spiegel, A A Schinzel
The Journal of Pediatrics|December 1, 1979
Monozygotic twinning and structural defectsA A Schinzel, D W Smith, J R Miller
Clinical Dysmorphology|January 1, 1994
An interstitial deletion of proximal 8q (q11-q13) in a girl with Silver-Russell syndrome-like featuresA A Schinzel, W P Robinson, F Binkert, et al.
Journal of Medical Genetics|May 1, 1994
Multiple origins of X chromosome tetrasomyW P Robinson, F Binkert, A A Schinzel, et al.
Journal of Medical Genetics|April 1, 1996
The dysmorphic human-mouse homology database (DHMHD): an interactive World-Wide Web resource for gene mappingC D Evans, A G Searle, A A Schinzel, et al.
Human Genetics|July 1, 1992
Reduced recombination and paternal age effect in Klinefelter syndromeI Lorda-Sanchez, F Binkert, M Maechler, et al.
American Journal of Human Genetics|February 1, 1992
No evidence for a paternal interchromosomal effect from analysis of the origin of nondisjunction in Down syndrome patients with concomitant familial chromosome rearrangementsA A Schinzel, P A Adelsberger, F Binkert, et al.
Pageof 4