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B Zoll

Showing results (31-40 of 63) with videos related to

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Fortschritte Der Neurologie-Psychiatrie|January 24, 2013
[X-linked recessive ichthyosis (XRI), cerebellar ataxia and neuropsychiatric symptoms]J R Pehlke, V Venkataramani, S Emmert, et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|May 1, 1993
Prenatal diagnosis of congenital nephrosis of the Finnish type (CNF) in the second trimesterA Suren, H J Gröne, M Kallerhoff, et al.
DNA and Cell Biology|December 19, 2001
Isolation and characterization of the human forkhead gene FOXQ1A Bieller, B Pasche, S Frank, et al.
Thrombosis Research|February 1, 1991
A single base-pair deletion in the protein C gene causing recurrent thromboembolismC Grundy, H Plendl, W Grote, et al.
Human Genetics|May 1, 1991
Carrier detection in haemophilia A by direct analysis of factor VIII gene lesionsD S Millar, P J Green, B Zoll, et al.
Human Reproduction (Oxford, England)|November 18, 1997
Relevance of genetic counselling in couples prior to intracytoplasmic sperm injectionH U Pauer, B Hinney, H W Michelmann, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Paramyotonia congenita and myotonic dystrophy are not allelic disordersM Koch, H Harley, T Grimm, et al.
Cytogenetic and Genome Research|June 12, 2008
Impairment of gastric acid secretion and increase of embryonic lethality in Foxq1-deficient miceW Goering, I M Adham, B Pasche, et al.
Human Genetics|May 1, 1989
Myotonia congenita (Thomsen's disease) excluded from the region of the myotonic dystrophy locus on chromosome 19M Koch, H Harley, M Sarfarazi, et al.
American Journal of Medical Genetics. Part A|July 29, 2003
Autistic disorder and chromosomal mosaicism 46,XY[123]/46,XY,del(20)(pter --> p12.2)[10]S Sauter, G von Beust, P Burfeind, et al.
Pageof 7

Showing results (31-40 of 63) with videos related to

Sort By:
Pageof 7
Fortschritte Der Neurologie-Psychiatrie|January 24, 2013
[X-linked recessive ichthyosis (XRI), cerebellar ataxia and neuropsychiatric symptoms]J R Pehlke, V Venkataramani, S Emmert, et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|May 1, 1993
Prenatal diagnosis of congenital nephrosis of the Finnish type (CNF) in the second trimesterA Suren, H J Gröne, M Kallerhoff, et al.
DNA and Cell Biology|December 19, 2001
Isolation and characterization of the human forkhead gene FOXQ1A Bieller, B Pasche, S Frank, et al.
Thrombosis Research|February 1, 1991
A single base-pair deletion in the protein C gene causing recurrent thromboembolismC Grundy, H Plendl, W Grote, et al.
Human Genetics|May 1, 1991
Carrier detection in haemophilia A by direct analysis of factor VIII gene lesionsD S Millar, P J Green, B Zoll, et al.
Human Reproduction (Oxford, England)|November 18, 1997
Relevance of genetic counselling in couples prior to intracytoplasmic sperm injectionH U Pauer, B Hinney, H W Michelmann, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Paramyotonia congenita and myotonic dystrophy are not allelic disordersM Koch, H Harley, T Grimm, et al.
Cytogenetic and Genome Research|June 12, 2008
Impairment of gastric acid secretion and increase of embryonic lethality in Foxq1-deficient miceW Goering, I M Adham, B Pasche, et al.
Human Genetics|May 1, 1989
Myotonia congenita (Thomsen's disease) excluded from the region of the myotonic dystrophy locus on chromosome 19M Koch, H Harley, M Sarfarazi, et al.
American Journal of Medical Genetics. Part A|July 29, 2003
Autistic disorder and chromosomal mosaicism 46,XY[123]/46,XY,del(20)(pter --> p12.2)[10]S Sauter, G von Beust, P Burfeind, et al.
Pageof 7