Neumann LM - Search Results

1

De novo terminal deletion of chromosome 15q26.1 characterised by comparative genomic hybridisation and FISH with locus specific probes.

Tönnies H, Schulze I, Hennies H, Neumann LM, Keitzer R, Neitzel H. Tönnies H, et al. Among authors: neumann lm. J Med Genet. 2001 Sep;38(9):617-21. doi: 10.1136/jmg.38.9.617. J Med Genet. 2001. PMID: 11565548 Free PMC article. No abstract available.

2

Characterization of a supernumerary ring chromosome 1 mosaicism in two cell systems by molecular cytogenetic techniques and review of the literature.

Tönnies H, Neumann LM, Grüneberg B, Neitzel H. Tönnies H, et al. Among authors: neumann lm. Am J Med Genet A. 2003 Aug 30;121A(2):163-7. doi: 10.1002/ajmg.a.20225. Am J Med Genet A. 2003. PMID: 12910498

3

Two further cases of WHS with unbalanced de novo translocation t(4;8) characterised by CGH and FISH.

Tönnies H, Stumm M, Neumann L, Volleth M, Grumpelt U, Müsebeck J, Annuss G, Neitzel H. Tönnies H, et al. J Med Genet. 2001 Jun;38(6):E21. doi: 10.1136/jmg.38.6.e21. J Med Genet. 2001. PMID: 11389168 Free PMC article. No abstract available.

4

Molecular cytogenetic identification and characterization of a de novo supernumerary neocentromeric derivative chromosome 13.

Tonnies H, Gerlach A, Heineking B, Starke H, Neitzel H, Neumann LM. Tonnies H, et al. Among authors: neumann lm. Cytogenet Genome Res. 2006;114(3-4):325-9. doi: 10.1159/000094221. Cytogenet Genome Res. 2006. PMID: 16954674

5

Premature chromosome condensation in humans associated with microcephaly and mental retardation: a novel autosomal recessive condition.

Neitzel H, Neumann LM, Schindler D, Wirges A, Tönnies H, Trimborn M, Krebsova A, Richter R, Sperling K. Neitzel H, et al. Among authors: neumann lm. Am J Hum Genet. 2002 Apr;70(4):1015-22. doi: 10.1086/339518. Epub 2002 Feb 20. Am J Hum Genet. 2002. PMID: 11857108 Free PMC article.

6

Ulnar-mammary syndrome with dysmorphic facies and mental retardation caused by a novel 1.28 Mb deletion encompassing the TBX3 gene.

Klopocki E, Neumann LM, Tönnies H, Ropers HH, Mundlos S, Ullmann R. Klopocki E, et al. Among authors: neumann lm. Eur J Hum Genet. 2006 Dec;14(12):1274-9. doi: 10.1038/sj.ejhg.5201696. Epub 2006 Aug 9. Eur J Hum Genet. 2006. PMID: 16896345

7

Mutations in microcephalin cause aberrant regulation of chromosome condensation.

Trimborn M, Bell SM, Felix C, Rashid Y, Jafri H, Griffiths PD, Neumann LM, Krebs A, Reis A, Sperling K, Neitzel H, Jackson AP. Trimborn M, et al. Among authors: neumann lm. Am J Hum Genet. 2004 Aug;75(2):261-6. doi: 10.1086/422855. Epub 2004 Jun 15. Am J Hum Genet. 2004. PMID: 15199523 Free PMC article.

8

A complex phenotype with cystic renal disease.

Müller D, Klopocki E, Neumann LM, Mundlos S, Taupitz M, Schulze I, Ropers HH, Querfeld U, Ullmann R. Müller D, et al. Among authors: neumann lm. Kidney Int. 2006 Nov;70(9):1656-60. doi: 10.1038/sj.ki.5001746. Epub 2006 Aug 16. Kidney Int. 2006. PMID: 16912708 Free article. No abstract available.

9

Shprintzen-Goldberg syndrome: fourteen new patients and a clinical analysis.

Robinson PN, Neumann LM, Demuth S, Enders H, Jung U, König R, Mitulla B, Müller D, Muschke P, Pfeiffer L, Prager B, Somer M, Tinschert S. Robinson PN, et al. Among authors: neumann lm. Am J Med Genet A. 2005 Jun 15;135(3):251-62. doi: 10.1002/ajmg.a.30431. Am J Med Genet A. 2005. PMID: 15884042

10

A new observation of two cases of acrofacial dysostosis type Genée-Wiedemann in a family--remarks on the mode of inheritance: report on two sibs.

Neumann L, Pelz J, Kunze J. Neumann L, et al. Am J Med Genet. 1996 Sep 6;64(4):556-62. doi: 10.1002/(SICI)1096-8628(19960906)64:4<556::AID-AJMG6>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8870922

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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

77 results

Search Page