Theile U - Search Results

1

Patient with Kabuki syndrome and acute leukemia.

Scherer S, Theile U, Beyer V, Ferrari R, Kreck C, Rister M. Scherer S, et al. Among authors: theile u. Am J Med Genet A. 2003 Sep 15;122A(1):76-9. doi: 10.1002/ajmg.a.20261. Am J Med Genet A. 2003. PMID: 12949977

2

[Siblings with neonatal progeroid syndrome (Wiedemann-Rautenstrauch)].

Hoppen T, Naumann A, Theile U, Rister M. Hoppen T, et al. Among authors: theile u. Klin Padiatr. 2004 Mar-Apr;216(2):70-1. doi: 10.1055/s-2004-44895. Klin Padiatr. 2004. PMID: 15106077 German.

3

[Neonatal progeroid syndrome (Wiedemann-Rautenstrauch syndrome): case report and review of the literature].

Hoppen T, Hausser I, Theile U, Ferrari R, Müller W, Rister M. Hoppen T, et al. Among authors: theile u. Klin Padiatr. 2000 Mar-Apr;212(2):71-6. doi: 10.1055/s-2000-9655. Klin Padiatr. 2000. PMID: 10812556 German.

4

[Noonan's syndrome with an unusual combination of hypertrophic cardiomyopathy, congenital bicuspid aortic valve, coarctation of the aorta and hypoplastic aortic arch].

Petersen SE, Mohrs OK, Theile U, Pohlmann W, Voigtländer T. Petersen SE, et al. Among authors: theile u. Z Kardiol. 2004 Apr;93(4):310-6. doi: 10.1007/s00392-004-0051-y. Z Kardiol. 2004. PMID: 15085376 German.

5

Syndrome of autosomal recessive polycystic kidneys with skeletal and facial anomalies is not linked to the ARPKD gene locus on chromosome 6p.

Hallermann C, Mücher G, Kohlschmidt N, Wellek B, Schumacher R, Bahlmann F, Shahidi-Asl P, Theile U, Rudnik-Schöneborn S, Müntefering H, Zerres K. Hallermann C, et al. Among authors: theile u. Am J Med Genet. 2000 Jan 17;90(2):115-9. doi: 10.1002/(sici)1096-8628(20000117)90:2<115::aid-ajmg5>3.0.co;2-s. Am J Med Genet. 2000. PMID: 10607948 Review.

6

A previously unrecognised phenotype characterised by obesity, muscular hypotonia, and ability to speak in patients with Angelman syndrome caused by an imprinting defect.

Gillessen-Kaesbach G, Demuth S, Thiele H, Theile U, Lich C, Horsthemke B. Gillessen-Kaesbach G, et al. Among authors: theile u. Eur J Hum Genet. 1999 Sep;7(6):638-44. doi: 10.1038/sj.ejhg.5200362. Eur J Hum Genet. 1999. PMID: 10482951

7

Patchy dermal hypoplasia as a characteristic feature of Proteus syndrome.

Happle R, Steijlen PM, Theile U, Karitzky D, Tinschert S, Albrecht-Nebe H, Küster W. Happle R, et al. Among authors: theile u. Arch Dermatol. 1997 Jan;133(1):77-80. Arch Dermatol. 1997. PMID: 9006375 Free article.

8

Mutations of the androgen receptor gene in patients with complete androgen insensitivity.

Jakubiczka S, Nedel S, Werder EA, Schleiermacher E, Theile U, Wolff G, Wieacker P. Jakubiczka S, et al. Among authors: theile u. Hum Mutat. 1997;9(1):57-61. doi: 10.1002/(SICI)1098-1004(1997)9:1<57::AID-HUMU10>3.0.CO;2-O. Hum Mutat. 1997. PMID: 8990010 No abstract available.

9

Microdissection and DOP-PCR-based reverse chromosome painting as a fast and reliable strategy in the analysis of various structural chromosome abnormalities.

Müller-Navia J, Nebel A, Oehler D, Theile U, Zabel B, Schleiermacher E. Müller-Navia J, et al. Among authors: theile u. Prenat Diagn. 1996 Oct;16(10):915-22. doi: 10.1002/(SICI)1097-0223(199610)16:10<915::AID-PD966>3.0.CO;2-V. Prenat Diagn. 1996. PMID: 8938060

10

[Tumor therapy and family planning].

Theile U, Rapp E. Theile U, et al. Med Klin (Munich). 1996 Jun 15;91(6):402-9. Med Klin (Munich). 1996. PMID: 8767316 Review. German. No abstract available.

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

47 results

Search Page

Filters