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L M Neumann

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Journal of Medical Genetics|September 22, 2001

De novo terminal deletion of chromosome 15q26.1 characterised by comparative genomic hybridisation and FISH with locus specific probesH Tönnies, I Schulze, H Hennies, et al.

Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|July 5, 2006

[Ocular manifestations and surgical results in patients with Marfan syndrome]M S Ladewig, P N Robinson, L M Neumann, et al.

Journal of Inherited Metabolic Disease|January 26, 2006

Smith-Lemli-Opitz syndrome with a classical phenotype, oesophageal achalasia and borderline plasma sterol concentrationsD Haas, S Armbrust, J-P Haas, et al.

Kidney International|August 17, 2006

A complex phenotype with cystic renal diseaseD Müller, E Klopocki, L M Neumann, et al.

Pageof 2

Search research articles

Showing results (11-20 of 14) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 14 results.

Journal of Medical Genetics|September 22, 2001

De novo terminal deletion of chromosome 15q26.1 characterised by comparative genomic hybridisation and FISH with locus specific probesH Tönnies, I Schulze, H Hennies, et al.

Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|July 5, 2006

[Ocular manifestations and surgical results in patients with Marfan syndrome]M S Ladewig, P N Robinson, L M Neumann, et al.

Journal of Inherited Metabolic Disease|January 26, 2006

Smith-Lemli-Opitz syndrome with a classical phenotype, oesophageal achalasia and borderline plasma sterol concentrationsD Haas, S Armbrust, J-P Haas, et al.

Kidney International|August 17, 2006

A complex phenotype with cystic renal diseaseD Müller, E Klopocki, L M Neumann, et al.

Pageof 2