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Human Genetics
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September 1, 1994
ICF syndrome: a new case and review of the literature
D F Smeets, U Moog, C M Weemaes, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
March 26, 2017
At first sight or second glance: clinical presentation of mosaic manifestations of autosomal dominant skin disorders - a case series
F Toberer, R Happle, R Schneiderbauer, et al.
American Journal of Medical Genetics. Part A
|
September 11, 2003
Rett syndrome in adolescent and adult females: clinical and molecular genetic findings
E Smeets, E Schollen, U Moog, et al.
Genetic Counseling (Geneva, Switzerland)
|
August 9, 2001
Lateral facial clefts: a case report
C E de Die-Smulders, U Moog, J J Engelen, et al.
Genetic Counseling (Geneva, Switzerland)
|
April 16, 2004
Hereditary motor and sensory neuropathy (HMSN) IA, developmental delay and autism related disorder in a boy with duplication (17)(p11.2p12)
U Moog, J J Engelen, B W Weber, et al.
Molecular Syndromology
|
January 18, 2013
5q31 Microdeletions: Definition of a Critical Region and Analysis of LRRTM2, a Candidate Gene for Intellectual Disability
W Kleffmann, A M Zink, J A Lee, et al.
New Microbes and New Infections
|
November 14, 2015
Acute Q fever infection in Thuringia, Germany, after burial of roe deer fawn cadavers (Capreolus capreolus): a case report
B T Schleenvoigt, L D Sprague, K Mertens, et al.
American Journal of Medical Genetics. Part A
|
June 5, 2003
Deletion of chromosome region 18q21.1 --> 18q21.3 in a patient without clinical features of the 18q- phenotype
J J M Engelen, U Moog, J Weber, et al.
Clinical Genetics
|
August 5, 2010
Pseudoautosomal inheritance of Léri-Weill syndrome: what does it mean?
C Evers, P H Heidemann, D Dunstheimer, et al.
Journal of Inherited Metabolic Disease
|
August 18, 2009
Mental retardation and inborn errors of metabolism
A García-Cazorla, N I Wolf, M Serrano, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 46) with videos related to
Sort By:
Page
of 5
Human Genetics
|
September 1, 1994
ICF syndrome: a new case and review of the literature
D F Smeets, U Moog, C M Weemaes, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
March 26, 2017
At first sight or second glance: clinical presentation of mosaic manifestations of autosomal dominant skin disorders - a case series
F Toberer, R Happle, R Schneiderbauer, et al.
American Journal of Medical Genetics. Part A
|
September 11, 2003
Rett syndrome in adolescent and adult females: clinical and molecular genetic findings
E Smeets, E Schollen, U Moog, et al.
Genetic Counseling (Geneva, Switzerland)
|
August 9, 2001
Lateral facial clefts: a case report
C E de Die-Smulders, U Moog, J J Engelen, et al.
Genetic Counseling (Geneva, Switzerland)
|
April 16, 2004
Hereditary motor and sensory neuropathy (HMSN) IA, developmental delay and autism related disorder in a boy with duplication (17)(p11.2p12)
U Moog, J J Engelen, B W Weber, et al.
Molecular Syndromology
|
January 18, 2013
5q31 Microdeletions: Definition of a Critical Region and Analysis of LRRTM2, a Candidate Gene for Intellectual Disability
W Kleffmann, A M Zink, J A Lee, et al.
New Microbes and New Infections
|
November 14, 2015
Acute Q fever infection in Thuringia, Germany, after burial of roe deer fawn cadavers (Capreolus capreolus): a case report
B T Schleenvoigt, L D Sprague, K Mertens, et al.
American Journal of Medical Genetics. Part A
|
June 5, 2003
Deletion of chromosome region 18q21.1 --> 18q21.3 in a patient without clinical features of the 18q- phenotype
J J M Engelen, U Moog, J Weber, et al.
Clinical Genetics
|
August 5, 2010
Pseudoautosomal inheritance of Léri-Weill syndrome: what does it mean?
C Evers, P H Heidemann, D Dunstheimer, et al.
Journal of Inherited Metabolic Disease
|
August 18, 2009
Mental retardation and inborn errors of metabolism
A García-Cazorla, N I Wolf, M Serrano, et al.
Page
of 5