Reichenbach H - Search Results

1

Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome.

Kohlhase J, Wischermann A, Reichenbach H, Froster U, Engel W. Kohlhase J, et al. Among authors: reichenbach h. Nat Genet. 1998 Jan;18(1):81-3. doi: 10.1038/ng0198-81. Nat Genet. 1998. PMID: 9425907

2

De novo complete trisomy 5p: clinical report and FISH studies.

Reichenbach H, Holland H, Dalitz E, Demandt C, Meiner A, Chudoba I, Lemke J, Claussen U, Froster UG. Reichenbach H, et al. Am J Med Genet. 1999 Aug 27;85(5):447-51. doi: 10.1002/(sici)1096-8628(19990827)85:5<447::aid-ajmg3>3.0.co;2-5. Am J Med Genet. 1999. PMID: 10405440 Review.

3

Hereditary congenital posterior dislocation of radial heads.

Reichenbach H, Hörmann D, Theile H. Reichenbach H, et al. Am J Med Genet. 1995 Jan 2;55(1):101-4. doi: 10.1002/ajmg.1320550124. Am J Med Genet. 1995. PMID: 7702079

4

[A further case with Baller-Gerold syndrome (craniosynostosis--radial aplasia syndrome)--overview and new viewpoints on a rare syndrome].

Reichenbach H, Hörmann D, Theile H. Reichenbach H, et al. Kinderarztl Prax. 1993 Jun;61(4-5):161-7. Kinderarztl Prax. 1993. PMID: 8361146 Review. German.

5

[Brachydactyly type A4 (brachymesophalangia II and V, Temtamy type). A rare type of brachydactyly].

Reichenbach H, Hörmann D, Theile H. Reichenbach H, et al. Kinderarztl Prax. 1993 Mar;61(2):59-62. Kinderarztl Prax. 1993. PMID: 8510402 German.

6

[Multiple abnormalities in a child with male karyotype due to familial partial Xp duplication].

Reichenbach H, Holland H, Thamm B, Theile T. Reichenbach H, et al. Kinderarztl Prax. 1993 Oct;61(7-8):291-5. Kinderarztl Prax. 1993. PMID: 8271681 German.

7

Trisomy of 5p and marker chromosomes.

Froster UG, Reichenbach H. Froster UG, et al. Among authors: reichenbach h. Am J Med Genet. 2000 Jul 3;93(1):76. doi: 10.1002/1096-8628(20000703)93:1<76::aid-ajmg13>3.0.co;2-g. Am J Med Genet. 2000. PMID: 10861686 No abstract available.

8

[The heart-hand syndrome. A new variant of disorders of heart conduction and syndactylia including osseous changes in hands and feet].

Reichenbach H, Meister EM, Theile H. Reichenbach H, et al. Kinderarztl Prax. 1992 Apr;60(2):54-6. Kinderarztl Prax. 1992. PMID: 1318983 German.

9

[Roberts syndrome with aneurysm of the interatrial septum, cow milk protein intolerance and absent swallowing reflex].

Scholbach T, Reichenbach H. Scholbach T, et al. Among authors: reichenbach h. Klin Padiatr. 1994 Nov-Dec;206(6):447-51. doi: 10.1055/s-2008-1046649. Klin Padiatr. 1994. PMID: 7823531 German.

10

Mapping of the bovine spinal muscular atrophy locus to Chromosome 24.

Medugorac I, Kemter J, Russ I, Pietrowski D, Nüske S, Reichenbach HD, Schmahl W, Förster M. Medugorac I, et al. Mamm Genome. 2003 Jun;14(6):383-91. doi: 10.1007/s00335-002-3024-3. Mamm Genome. 2003. PMID: 12879360

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