Format
Sort by
Items per page

Send to

Choose Destination

Links from Books

Items: 17

1.

The clinical phenotype of mosaicism for genome-wide paternal uniparental disomy: two new reports.

Wilson M, Peters G, Bennetts B, McGillivray G, Wu ZH, Poon C, Algar E.

Am J Med Genet A. 2008 Jan 15;146A(2):137-48.

PMID:
18033734
2.

Chromosome 11 segmental paternal isodisomy in amniocytes from two fetuses with omphalocoele: new highlights on phenotype-genotype correlations in Beckwith-Wiedemann syndrome.

Grati FR, Turolla L, D'Ajello P, Ruggeri A, Miozzo M, Bracalente G, Baldo D, Laurino L, Boldorini R, Frate E, Surico N, Larizza L, Maggi F, Simoni G.

J Med Genet. 2007 Apr;44(4):257-63.

3.
4.

Somatic mosaicism for partial paternal isodisomy in Wiedemann-Beckwith syndrome: a post-fertilization event.

Henry I, Puech A, Riesewijk A, Ahnine L, Mannens M, Beldjord C, Bitoun P, Tournade MF, Landrieu P, Junien C.

Eur J Hum Genet. 1993;1(1):19-29.

PMID:
8069648
5.
6.

Genetic fine-structure mapping in human chromosome 11 by use of repetitive DNA sequences.

Gusella JF, Jones C, Kao FT, Housman D, Puck TT.

Proc Natl Acad Sci U S A. 1982 Dec;79(24):7804-8.

7.

Assignment of the human parathyroid hormone gene to chromosome 11.

Mayer H, Breyel E, Bostock C, Schmidtke J.

Hum Genet. 1983;64(3):283-5.

PMID:
6885073
8.

High-resolution chromosome sorting and DNA spot-blot analysis assign McArdle's syndrome to chromosome 11.

Lebo RV, Gorin F, Fletterick RJ, Kao FT, Cheung MC, Bruce BD, Kan YW.

Science. 1984 Jul 6;225(4657):57-9.

PMID:
6587566
9.

Chromosomal assignment of a family of human oncogenes.

Ryan J, Barker PE, Shimizu K, Wigler M, Ruddle FH.

Proc Natl Acad Sci U S A. 1983 Jul;80(14):4460-3.

10.

Aneuploidy in recurrent spontaneous aborters: the tendency to parental nondisjunction.

Hecht F, Hecht BK, Berger CS.

Clin Genet. 1984 Jul;26(1):43-5.

PMID:
6467654
11.

Identification of translocation chromosomes by quinacrine fluorescence.

Breg WR, Miller DA, Allderdice PW, Miller OJ.

Am J Dis Child. 1972 Jun;123(6):561-4. No abstract available.

PMID:
4113489
12.

High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones.

Lichter P, Tang CJ, Call K, Hermanson G, Evans GA, Housman D, Ward DC.

Science. 1990 Jan 5;247(4938):64-9.

PMID:
2294592
13.

Balanced chromosome rearrangements and abnormal phenotype.

Kosztolányi G, Bajnóczky K, Méhes K.

Acta Paediatr Hung. 1991;31(4):397-402.

PMID:
1790022
14.

Duplication of chromosome 11 centromere in fetal and maternal karyotypes: a new variant?

Till M, Rafat A, Charrin C, Plauchu H, Germain D.

Prenat Diagn. 1991 Jul;11(7):481-2.

PMID:
1754567
15.

Chromosome 11 uniparental isodisomy predisposing to embryonal neoplasms.

Grundy P, Telzerow P, Paterson MC, Haber D, Berman B, Li F, Garber J.

Lancet. 1991 Oct 26;338(8774):1079-80. No abstract available.

PMID:
1681381
16.

A microchromosome derived from chromosome 11 in a patient with the CREST syndrome of scleroderma.

Haaf T, Sumner AT, Köhler J, Willard HF, Schmid M.

Cytogenet Cell Genet. 1992;60(1):12-7. Erratum in: Cytogenet Cell Genet 1992;61(3):following 223. Summer AT [corrected to Sumner AT].

PMID:
1582251
17.

A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH).

Rauch A, Pfeiffer RA, Trautmann U, Liehr T, Rott HD, Ulmer R.

Clin Genet. 1992 Aug;42(2):84-90.

PMID:
1424236

Supplemental Content

Support Center