Binkert F - Search Results

1

New immortalized cell lines of patients with small supernumerary marker chromosome: towards the establishment of a cell bank.

Tönnies H, Pietrzak J, Bocian E, MacDermont K, Kuechler A, Belitz B, Trautmann U, Schmidt A, Schulze B, Rodríguez L, Binkert F, Yardin C, Kosyakova N, Volleth M, Mkrtchyan H, Schreyer I, von Eggeling F, Weise A, Mrasek K, Liehr T. Tönnies H, et al. Among authors: binkert f. J Histochem Cytochem. 2007 Jun;55(6):651-60. doi: 10.1369/jhc.6A7161.2007. Epub 2007 Mar 6. J Histochem Cytochem. 2007. PMID: 17341473

2

Complex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity?

Trifonov V, Fluri S, Binkert F, Nandini A, Anderson J, Rodriguez L, Gross M, Kosyakova N, Mkrtchyan H, Ewers E, Reich D, Weise A, Liehr T. Trifonov V, et al. Among authors: binkert f. Mol Cytogenet. 2008 Apr 15;1:6. doi: 10.1186/1755-8166-1-6. Mol Cytogenet. 2008. PMID: 18471318 Free PMC article.

3

Uniparental origin of sex chromosome polysomies.

Lorda-Sanchez I, Binkert F, Hinkel KG, Moser H, Rosenkranz W, Maechler M, Schinzel A. Lorda-Sanchez I, et al. Among authors: binkert f. Hum Hered. 1992;42(3):193-7. doi: 10.1159/000154066. Hum Hered. 1992. PMID: 1512000

4

Parental origin of the supernumerary chromosome in trisomy 18.

Ya-gang X, Robinson WP, Spiegel R, Binkert F, Ruefenacht U, Schinzel AA. Ya-gang X, et al. Among authors: binkert f. Clin Genet. 1993 Aug;44(2):57-61. doi: 10.1111/j.1399-0004.1993.tb03847.x. Clin Genet. 1993. PMID: 8275560

5

A 48,XXY,+21 Down syndrome patient with additional paternal X and maternal 21.

Lorda-Sanchez I, Petersen MB, Binkert F, Maechler M, Schmid W, Adelsberger PA, Antonarakis SE, Schinzel A. Lorda-Sanchez I, et al. Among authors: binkert f. Hum Genet. 1991 May;87(1):54-6. doi: 10.1007/BF01213092. Hum Genet. 1991. PMID: 1674717

6

A molecular study of X isochromosomes: parental origin, centromeric structure, and mechanisms of formation.

Lorda-Sanchez I, Binkert F, Maechler M, Schinzel A. Lorda-Sanchez I, et al. Among authors: binkert f. Am J Hum Genet. 1991 Nov;49(5):1034-40. Am J Hum Genet. 1991. PMID: 1681727 Free PMC article.

7

Partial trisomy of chromosome 18 (pter----q12) following a familial 18;21 translocation rcp(18;21)(q12;q11).

Binkert F, Stranzinger J, Schinzel A. Binkert F, et al. Hum Hered. 1990;40(2):81-4. doi: 10.1159/000153910. Hum Hered. 1990. PMID: 2335369

8

Molecular studies of chromosomal mosaicism: relative frequency of chromosome gain or loss and possible role of cell selection.

Robinson WP, Binkert F, Bernasconi F, Lorda-Sanchez I, Werder EA, Schinzel AA. Robinson WP, et al. Among authors: binkert f. Am J Hum Genet. 1995 Feb;56(2):444-51. Am J Hum Genet. 1995. PMID: 7847381 Free PMC article.

9

Clinical and molecular analysis of five inv dup(15) patients.

Robinson WP, Binkert F, Giné R, Vazquez C, Müller W, Rosenkranz W, Schinzel A. Robinson WP, et al. Among authors: binkert f. Eur J Hum Genet. 1993;1(1):37-50. doi: 10.1159/000472386. Eur J Hum Genet. 1993. PMID: 8069650

10

Molecular study of 45,X conceptuses: correlation with clinical findings.

Lorda-Sanchez I, Binkert F, Maechler M, Schinzel A. Lorda-Sanchez I, et al. Among authors: binkert f. Am J Med Genet. 1992 Feb 15;42(4):487-90. doi: 10.1002/ajmg.1320420414. Am J Med Genet. 1992. PMID: 1351700

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

56 results

Search Page

Filters