Zankl A - Search Results

1

New chimaeric hepatitis B virus core particles carrying hantavirus (serotype Puumala) epitopes: immunogenicity and protection against virus challenge.

Ulrich R, Koletzki D, Lachmann S, Lundkvist A, Zankl A, Kazaks A, Kurth A, Gelderblom HR, Borisova G, Meisel H, Krüger DH. Ulrich R, et al. Among authors: zankl a. J Biotechnol. 1999 Aug 20;73(2-3):141-53. doi: 10.1016/s0168-1656(99)00117-0. J Biotechnol. 1999. PMID: 10486924 Review.

2

[Fluorescent in situ hybridization (FISH). Diagnostic aide in certain chromosomal anomalies].

Zankl A, Addor MC, Thonney F, Gaide AC, Schorderet DF. Zankl A, et al. Rev Med Suisse Romande. 2000 May;120(5):389-92. Rev Med Suisse Romande. 2000. PMID: 10911741 French. No abstract available.

3

A characteristic EEG pattern in 4p-syndrome: case report and review of the literature.

Zankl A, Addor MC, Maeder-Ingvar MM, Schorderet DF. Zankl A, et al. Eur J Pediatr. 2001 Feb;160(2):123-7. doi: 10.1007/s004310000679. Eur J Pediatr. 2001. PMID: 11271384 Review.

4

Defective DNA Polymerase α-Primase Leads to X-Linked Intellectual Disability Associated with Severe Growth Retardation, Microcephaly, and Hypogonadism.

Van Esch H, Colnaghi R, Freson K, Starokadomskyy P, Zankl A, Backx L, Abramowicz I, Outwin E, Rohena L, Faulkner C, Leong GM, Newbury-Ecob RA, Challis RC, Õunap K, Jaeken J, Seuntjens E, Devriendt K, Burstein E, Low KJ, O'Driscoll M. Van Esch H, et al. Among authors: zankl a. Am J Hum Genet. 2019 May 2;104(5):957-967. doi: 10.1016/j.ajhg.2019.03.006. Epub 2019 Apr 18. Am J Hum Genet. 2019. PMID: 31006512 Free PMC article.

5

Prenatal and postnatal presentation of severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN) due to the FGFR3 Lys650Met mutation.

Zankl A, Elakis G, Susman RD, Inglis G, Gardener G, Buckley MF, Roscioli T. Zankl A, et al. Am J Med Genet A. 2008 Jan 15;146A(2):212-8. doi: 10.1002/ajmg.a.32085. Am J Med Genet A. 2008. PMID: 18076102

6

Natural history of twin disruption sequence.

Zankl A, Brooks D, Boltshauser E, Largo R, Schinzel A. Zankl A, et al. Am J Med Genet A. 2004 Jun 1;127A(2):133-8. doi: 10.1002/ajmg.a.20680. Am J Med Genet A. 2004. PMID: 15108199

7

Spondyloperipheral dysplasia is caused by truncating mutations in the C-propeptide of COL2A1.

Zankl A, Zabel B, Hilbert K, Wildhardt G, Cuenot S, Xavier B, Ha-Vinh R, Bonafé L, Spranger J, Superti-Furga A. Zankl A, et al. Am J Med Genet A. 2004 Aug 30;129A(2):144-8. doi: 10.1002/ajmg.a.30222. Am J Med Genet A. 2004. PMID: 15316962

8

Novel mutation in the tyrosine kinase domain of FGFR2 in a patient with Pfeiffer syndrome.

Zankl A, Jaeger G, Bonafé L, Boltshauser E, Superti-Furga A. Zankl A, et al. Am J Med Genet A. 2004 Dec 15;131(3):299-300. doi: 10.1002/ajmg.a.30366. Am J Med Genet A. 2004. PMID: 15523615

9

Computer-aided anthropometry in the evaluation of dysmorphic children.

Zankl A. Zankl A. Pediatrics. 2004 Sep;114(3):e333-6. doi: 10.1542/peds.2004-0045. Pediatrics. 2004. PMID: 15342894

10

Juvenile myoclonic epilepsy with photosensitivity in a female with Velocardiofacial syndrome (del(22)(q11.2))--causal relationship or coincidence?

Lemke JR, Beck-Wödl S, Zankl A, Riegel M, Krämer G, Dorn T. Lemke JR, et al. Among authors: zankl a. Seizure. 2009 Nov;18(9):660-3. doi: 10.1016/j.seizure.2009.07.008. Epub 2009 Aug 19. Seizure. 2009. PMID: 19695908 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

114 results

Search Page

Filters