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American Journal of Medical Genetics|November 15, 1993

On the variability of the Brachmann-de Lange syndrome in seven patientsJ G Leroy, J Persijn, V Van de Weghe, et al.

Journal of Bacteriology|May 6, 2003

The yggH gene of Escherichia coli encodes a tRNA (m7G46) methyltransferaseLara G S De Bie, Martine Roovers, Yamina Oudjama, et al.

European Journal of Human Genetics : EJHG|January 1, 1996

Refined genetic and physical mapping of BPES type IIL Messiaen, B P Leroy, S De Bie, et al.

European Journal of Gastroenterology & Hepatology|September 21, 2001

Association between Cys282Tyr missense mutation and haptoglobin phenotype polymorphism in patients with chronic hepatitis CH Van Vlierberghe, J R Delanghe, S De Bie, et al.

American Journal of Medical Genetics|January 1, 1991

Pseudoxanthoma elasticum: similar autosomal recessive subtype in Belgian and Afrikaner familiesA De Paepe, D Viljoen, M Matton, et al.

International Journal of Biometeorology|February 19, 2013

Larger antelopes are sensitive to heat stress throughout all seasons but smaller antelopes only during summer in an African semi-arid environmentA K Shrestha, S E van Wieren, F van Langevelde, et al.

Alimentary Pharmacology & Therapeutics|August 30, 2012

Prescription of nonselective NSAIDs, coxibs and gastroprotective agents in the era of rofecoxib withdrawal - a 617,400-patient studyV E Valkhoff, E M van Soest, G M C Masclee, et al.

The Journal of Biological Chemistry|May 16, 2002

Physical interaction between GATA-5 and hepatocyte nuclear factor-1alpha results in synergistic activation of the human lactase-phlorizin hydrolase promoterHerbert M van Wering, Inge L Huibregtse, Sanne M van der Zwan, et al.

Human Mutation|February 19, 2000

Fifteen new mutations (-195C>T, L-12X, 298-2A>G, T117N, A159T, R229S, 997+2T>A, E274X, A331T, H364R, D389G, 1256delC, R433H, N461I, C472S) in the tissue-nonspecific alkaline phosphatase (TNSALP) gene in patients with hypophosphatasiaA Taillandier, E Cozien, F Muller, et al.

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Showing results (21-30 of 29) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 29 results.

American Journal of Medical Genetics|November 15, 1993

On the variability of the Brachmann-de Lange syndrome in seven patientsJ G Leroy, J Persijn, V Van de Weghe, et al.

Journal of Bacteriology|May 6, 2003

The yggH gene of Escherichia coli encodes a tRNA (m7G46) methyltransferaseLara G S De Bie, Martine Roovers, Yamina Oudjama, et al.

European Journal of Human Genetics : EJHG|January 1, 1996

Refined genetic and physical mapping of BPES type IIL Messiaen, B P Leroy, S De Bie, et al.

European Journal of Gastroenterology & Hepatology|September 21, 2001

Association between Cys282Tyr missense mutation and haptoglobin phenotype polymorphism in patients with chronic hepatitis CH Van Vlierberghe, J R Delanghe, S De Bie, et al.

American Journal of Medical Genetics|January 1, 1991

Pseudoxanthoma elasticum: similar autosomal recessive subtype in Belgian and Afrikaner familiesA De Paepe, D Viljoen, M Matton, et al.

International Journal of Biometeorology|February 19, 2013

Larger antelopes are sensitive to heat stress throughout all seasons but smaller antelopes only during summer in an African semi-arid environmentA K Shrestha, S E van Wieren, F van Langevelde, et al.

Alimentary Pharmacology & Therapeutics|August 30, 2012

Prescription of nonselective NSAIDs, coxibs and gastroprotective agents in the era of rofecoxib withdrawal - a 617,400-patient studyV E Valkhoff, E M van Soest, G M C Masclee, et al.

The Journal of Biological Chemistry|May 16, 2002

Physical interaction between GATA-5 and hepatocyte nuclear factor-1alpha results in synergistic activation of the human lactase-phlorizin hydrolase promoterHerbert M van Wering, Inge L Huibregtse, Sanne M van der Zwan, et al.

Human Mutation|February 19, 2000

Fifteen new mutations (-195C>T, L-12X, 298-2A>G, T117N, A159T, R229S, 997+2T>A, E274X, A331T, H364R, D389G, 1256delC, R433H, N461I, C472S) in the tissue-nonspecific alkaline phosphatase (TNSALP) gene in patients with hypophosphatasiaA Taillandier, E Cozien, F Muller, et al.

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