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Annales De Genetique|January 1, 1994
Isochromosome-formation in chromosome 9K Miller, M Arslan-KirchnerHNO|June 27, 2012
[Tetrasomy 18p syndrome and hearing loss. An unusual case]C Schwemmle, M Arslan-Kirchner, B Pabst, et al.Cytogenetic and Genome Research|March 9, 2004
The application of region-specific probes for the resolution of duplication 8p: a case report and a review of the literatureB Pabst, M Arslan-Kirchner, J Schmidtke, et al.Laryngo- Rhino- Otologie|September 23, 1998
[Congenital subglottic laryngeal stenosis in 2 brothers with chondrodysplasia syndrome (Keutel-Gabriel syndrome)]I Buchsteiner, H G Kempf, M Arslan-Kirchner, et al.International Journal of Legal Medicine|October 18, 2008
Marfan syndrome: clinical consequences resulting from a medicolegal autopsy of a case of sudden death due to aortic ruptureM Klintschar, U Bilkenroth, M Arslan-Kirchner, et al.European Journal of Pediatrics|December 11, 1999
A search for chromosome 22q11.2 deletions in a series of 176 consecutively catheterized patients with congenital heart disease: no evidence for deletions in non-syndromic patientsS Borgmann, I Luhmer, M Arslan-Kirchner, et al.Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|February 1, 1990
[Recurrent post-infectious immune complex glomerulonephritis with persistent activation of the alternative complement pathway]M Arslan-Kirchner, J H Ehrich, M Kirschfink, et al.Human Mutation|July 29, 1999
Identification of 9 novel FBN1 mutations in German patients with Marfan syndromeA A El-Aleem, M Karck, A Haverich, et al.American Journal of Medical Genetics|April 12, 2001
Patient with trisomy 6 mosaicismK R Miller, K Mühlhaus, R A Herbst, et al.Human Genetics|February 8, 2003
Chromosome 18 replaced by two ring chromosomes of chromosome 18 originK Miller, B Pabst, H Ritter, et al.Pageof 3