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Journal of Medical Genetics
|
July 4, 2009
Encephalocraniocutaneous lipomatosis
U Moog
European Journal of Neurology
|
February 15, 2012
How fingers and face can be the clue?
A Behnecke, N Dikow, U Moog
Journal of Clinical Ultrasound : JCU
|
May 8, 1998
Prenatal sonographic diagnosis of nuchal edema and double aneuploidy (48,XXY,+21): discrepancy between results of chorionic villi and amniotic fluid sampling
U Moog, G Hamers, H Hoogland
American Journal of Medical Genetics
|
December 26, 2001
Acampomelic campomelic syndrome
U Moog, N J Jansen, G Scherer, et al.
Journal of Medical Genetics
|
May 10, 2005
Oculocerebrocutaneous syndrome: the brain malformation defines a core phenotype
U Moog, M C Jones, L M Bird, et al.
Clinical Genetics
|
January 24, 1998
Oculocerebrocutaneous syndrome: report of three additional cases and aetiological considerations
U Moog, C de Die-Smulders, J M Systermans, et al.
Genetic Counseling (Geneva, Switzerland)
|
November 6, 2002
Wolf-Hirschhorn (4p-)syndrome in a near adult with major depression; successful treatment with citalopram
W M A Verhoeven, U Moog, A M A Wagemans, et al.
Clinical Genetics
|
September 30, 2011
Silver-Russell syndrome due to maternal uniparental disomy 7 and a familial reciprocal translocation t(7;13)
A Behnecke, K Hinderhofer, A Jauch, et al.
Clinical Dysmorphology
|
October 1, 1996
Alagille syndrome in a family with duplication 20p11
U Moog, J Engelen, J Albrechts, et al.
Genetic Counseling (Geneva, Switzerland)
|
October 20, 1998
Spasticity, mental retardation, macrocephaly and distinct craniofacial appearance: confirmation of a new subtype of complicated spastic paraplegia?
U Moog, A M Schoonbrood-Lenssen, C T Schrander-Stumpel, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 46) with videos related to
Sort By:
Page
of 5
Journal of Medical Genetics
|
July 4, 2009
Encephalocraniocutaneous lipomatosis
U Moog
European Journal of Neurology
|
February 15, 2012
How fingers and face can be the clue?
A Behnecke, N Dikow, U Moog
Journal of Clinical Ultrasound : JCU
|
May 8, 1998
Prenatal sonographic diagnosis of nuchal edema and double aneuploidy (48,XXY,+21): discrepancy between results of chorionic villi and amniotic fluid sampling
U Moog, G Hamers, H Hoogland
American Journal of Medical Genetics
|
December 26, 2001
Acampomelic campomelic syndrome
U Moog, N J Jansen, G Scherer, et al.
Journal of Medical Genetics
|
May 10, 2005
Oculocerebrocutaneous syndrome: the brain malformation defines a core phenotype
U Moog, M C Jones, L M Bird, et al.
Clinical Genetics
|
January 24, 1998
Oculocerebrocutaneous syndrome: report of three additional cases and aetiological considerations
U Moog, C de Die-Smulders, J M Systermans, et al.
Genetic Counseling (Geneva, Switzerland)
|
November 6, 2002
Wolf-Hirschhorn (4p-)syndrome in a near adult with major depression; successful treatment with citalopram
W M A Verhoeven, U Moog, A M A Wagemans, et al.
Clinical Genetics
|
September 30, 2011
Silver-Russell syndrome due to maternal uniparental disomy 7 and a familial reciprocal translocation t(7;13)
A Behnecke, K Hinderhofer, A Jauch, et al.
Clinical Dysmorphology
|
October 1, 1996
Alagille syndrome in a family with duplication 20p11
U Moog, J Engelen, J Albrechts, et al.
Genetic Counseling (Geneva, Switzerland)
|
October 20, 1998
Spasticity, mental retardation, macrocephaly and distinct craniofacial appearance: confirmation of a new subtype of complicated spastic paraplegia?
U Moog, A M Schoonbrood-Lenssen, C T Schrander-Stumpel, et al.
Page
of 5