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B Zoll

Showing results (21-30 of 63) with videos related to

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Clinical Genetics|January 1, 1993
Trisomy 13 (Patau syndrome) with an 11-year survivalB Zoll, J Wolf, D Lensing-Hebben, et al.
Journal of Medical Genetics|March 1, 1993
Direct versus indirect molecular diagnosis of fragile X mental retardation in 40 German families at riskO Knobloch, F Pelz, U Wick, et al.
Journal of Medical Genetics|August 6, 2002
MECP2 gene nucleotide changes and their pathogenicity in males: proceed with cautionF Laccone, B Zoll, P Huppke, et al.
Journal of Cancer Research and Clinical Oncology|January 1, 1992
Alterations of the c-erbB2 gene in human breast cancerB Zoll, B Kynast, B Corell, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|March 1, 1992
[Martin-Bell syndrome. Improved possibilities for molecular genetic diagnosis]B Zoll, J Bal, J Pohnke, et al.
Journal of Neurology|October 1, 1995
Distribution of epidermal growth factor receptor gene amplification in brain tumours and correlation to prognosisU Diedrich, J Lucius, E Baron, et al.
American Journal of Medical Genetics|July 27, 2001
Short stature in a mother and daughter caused by familial der(X)t(X;X)(p22.1-3;q26)T Reinehr, A Jauch, B Zoll, et al.
Cytogenetic and Genome Research|October 12, 2012
A family with an inverted tandem duplication 5q22.1q23.2T Schmidt, I Bartels, T Liehr, et al.
Human Genetics|September 1, 1991
The molecular genetics of haemophilia A: screening for point mutations in the factor VIII gene using the restriction enzyme TaqID S Millar, B Zoll, U Martinowitz, et al.
Human Genetics|August 1, 1993
Recurrent mutations in the factor IX gene: founder effect or repeat de novo events. Investigation of the German haemophilia B population and review of de novo mutationsO Knobloch, B Zoll, K Zerres, et al.
Pageof 7

Showing results (21-30 of 63) with videos related to

Sort By:
Pageof 7
Clinical Genetics|January 1, 1993
Trisomy 13 (Patau syndrome) with an 11-year survivalB Zoll, J Wolf, D Lensing-Hebben, et al.
Journal of Medical Genetics|March 1, 1993
Direct versus indirect molecular diagnosis of fragile X mental retardation in 40 German families at riskO Knobloch, F Pelz, U Wick, et al.
Journal of Medical Genetics|August 6, 2002
MECP2 gene nucleotide changes and their pathogenicity in males: proceed with cautionF Laccone, B Zoll, P Huppke, et al.
Journal of Cancer Research and Clinical Oncology|January 1, 1992
Alterations of the c-erbB2 gene in human breast cancerB Zoll, B Kynast, B Corell, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|March 1, 1992
[Martin-Bell syndrome. Improved possibilities for molecular genetic diagnosis]B Zoll, J Bal, J Pohnke, et al.
Journal of Neurology|October 1, 1995
Distribution of epidermal growth factor receptor gene amplification in brain tumours and correlation to prognosisU Diedrich, J Lucius, E Baron, et al.
American Journal of Medical Genetics|July 27, 2001
Short stature in a mother and daughter caused by familial der(X)t(X;X)(p22.1-3;q26)T Reinehr, A Jauch, B Zoll, et al.
Cytogenetic and Genome Research|October 12, 2012
A family with an inverted tandem duplication 5q22.1q23.2T Schmidt, I Bartels, T Liehr, et al.
Human Genetics|September 1, 1991
The molecular genetics of haemophilia A: screening for point mutations in the factor VIII gene using the restriction enzyme TaqID S Millar, B Zoll, U Martinowitz, et al.
Human Genetics|August 1, 1993
Recurrent mutations in the factor IX gene: founder effect or repeat de novo events. Investigation of the German haemophilia B population and review of de novo mutationsO Knobloch, B Zoll, K Zerres, et al.
Pageof 7