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American Journal of Medical Genetics|January 8, 1999
Microcephaly-lymphedema syndrome: report of a family with short stature as additional manifestationS Strenge, U G FrosterDer Nervenarzt|August 1, 1997
[Diagnostic problems in juvenile Huntington chorea]H Woldag, S Strenge, K WeiseKlinische Padiatrie|September 25, 2008
[Muscular hypotonia, developmental retardation, speech delay and mildly dysmorphic features: 22q13 deletion syndrome (Phelan-McDermid Syndrome) as an important differential diagnosis]S Strenge, U G Froster, A Kujat, et al.Prenatal Diagnosis|December 13, 2000
Prenatal diagnosis of del(15)(q26.1) and del(18)(q21.3) due to an unbalanced de novo translocation: ultrasound, molecular cytogenetic and autopsy findingsU G Froster, L C Horn, H Holland, et al.Cutis|August 12, 2022
Deployed Airbag Causes Bullous Reaction Following a Motor Vehicle AccidentKatlin R Poladian, Rechelle Tull, Karen S Strenge, et al.Laboratory Medicine|January 25, 2015
Utility of reflexive gomori methenamine silver and Acid-fast bacillus staining on bronchoalveolar lavage specimensKaren S Strenge, Julie E Kunkel, Alan A George, et al.Prenatal Diagnosis|March 12, 1999
Pitfalls in prenatal diagnosis of DMD due to placental mosaicism of the X-chromosomes: prenatal and postnatal findings in a fetus with a deletion of exons 67-71 of the dystrophin geneS Vondran, J Edelmann, H Holland, et al.Klinische Padiatrie|January 10, 2008
[Neurofibromatosis type 1 and associated clinical abnormalities in 27 children]S Syrbe, K Eberle, S Strenge, et al.Human Molecular Genetics|August 11, 1999
Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndromeM Kalff-Suske, A Wild, J Topp, et al.Pageof 1