Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 81

1.

Slot blot method for the quantification of DNA sequences and mapping of chromosome rearrangements: application to chromosome 21.

Blouin JL, Rahmani Z, Chettouh Z, Prieur M, Fermanian J, Poissonnier M, Leonard C, Nicole A, Mattei JF, Sinet PM, et al.

Am J Hum Genet. 1990 Mar;46(3):518-26.

2.

Regional mapping of unique DNA sequences from human chromosome 3 derived from a flow-sorted chromosome library.

Atchison LM, Naylor SL, Freed JJ, Comis RL.

Cytogenet Cell Genet. 1988;48(3):156-9.

PMID:
2906850
3.

Random-breakage mapping method applied to human DNA sequences.

Löbrich M, Rydberg B, Cooper PK.

Nucleic Acids Res. 1996 May 15;24(10):1802-8.

4.

The human catechol-O-methyltransferase (COMT) gene maps to band q11.2 of chromosome 22 and shows a frequent RFLP with BglI.

Winqvist R, Lundström K, Salminen M, Laatikainen M, Ulmanen I.

Cytogenet Cell Genet. 1992;59(4):253-7.

PMID:
1347500
5.

Detection of molecular rearrangements in Prader-Willi syndrome patients by using genomic probes recognizing four loci within the PWCR.

Gregory CA, Kirkilionis AJ, Greenberg CR, Chudley AE, Hamerton JL.

Am J Med Genet. 1990 Apr;35(4):536-45.

PMID:
1970703
6.

Gene-dosage mapping of 30 DNA markers on chromosome 21.

Delabar JM, Chettouh Z, Rahmani Z, Theophile D, Blouin JL, Bono R, Kraus J, Barton J, Patterson D, Sinet PM.

Genomics. 1992 Jul;13(3):887-9.

PMID:
1639420
7.

Determination of genomic copy number with quantitative microsphere hybridization.

Newkirk HL, Rogan PK, Miralles M, Knoll JH.

Hum Mutat. 2006 Apr;27(4):376-86. Erratum in: Hum Mutat. 2006 Jun;27(6):597.

PMID:
16541397
8.

Application of molecular and somatic cell genetics to the study of chromosome 21.

Law ML, Van Keuren M.

Ann N Y Acad Sci. 1986;477:151-9. Review.

PMID:
2880544
9.

Isolation and regional mapping of DNA sequences unique to human chromosome 21.

Korenberg JR, Croyle ML, Cox DR.

Am J Hum Genet. 1987 Dec;41(6):963-78.

10.

Molecular genetic approach to the characterization of the "Down syndrome region" of chromosome 21.

McCormick MK, Schinzel A, Petersen MB, Stetten G, Driscoll DJ, Cantu ES, Tranebjaerg L, Mikkelsen M, Watkins PC, Antonarakis SE.

Genomics. 1989 Aug;5(2):325-31.

PMID:
2529205
11.

Isolation and characterization of DNA probes for human chromosome 21.

Watkins PC.

Prog Clin Biol Res. 1990;360:53-67. Review.

PMID:
2247511
12.

Detection of DNA rearrangements in the AML1 and ETO loci and of an AML1/ETO fusion mRNA in patients with t(8;21) acute myeloid leukemia.

Nucifora G, Birn DJ, Erickson P, Gao J, LeBeau MM, Drabkin HA, Rowley JD.

Blood. 1993 Feb 15;81(4):883-8.

13.

Human testicular cancer. Changes in autosomal dosage.

Peltomäki P, Halme A, de la Chapelle A.

Cancer Genet Cytogenet. 1990 Aug 1;48(1):1-12.

PMID:
1973631
14.

Distribution of human endogenous retroviral RTVL-H2 LTR sequences among human chromosomes.

Sugino H, Oshimura M, Mastubara K.

Gene. 1997 Oct 1;198(1-2):83-7.

PMID:
9370267
15.

Sequence-based, in situ detection of chromosomal abnormalities at high resolution.

Knoll JH, Rogan PK.

Am J Med Genet A. 2003 Sep 1;121A(3):245-57.

PMID:
12923866
16.

Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome.

Rahmani Z, Blouin JL, Creau-Goldberg N, Watkins PC, Mattei JF, Poissonnier M, Prieur M, Chettouh Z, Nicole A, Aurias A, et al.

Proc Natl Acad Sci U S A. 1989 Aug;86(15):5958-62.

17.

Application of chromosome 4q35-qter marker (pFR-1) for DNA rearrangement of facioscapulohumeral muscular dystrophy patients in Taiwan.

Hsu YD, Kao MC, Shyu WC, Lin JC, Huang NE, Sun HF, Yang KD, Tsao WL.

J Neurol Sci. 1997 Jul;149(1):73-9.

PMID:
9168169
18.

Localization of a human brain sodium channel gene (SCN2A) to chromosome 2.

Litt M, Luty J, Kwak M, Allen L, Magenis RE, Mandel G.

Genomics. 1989 Aug;5(2):204-8.

PMID:
2571571
19.

Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.

Zhang L, Parkhurst JB, Kern WF, Scott KV, Niccum D, Mulvihill JJ, Li S.

Chin Med J (Engl). 2003 Sep;116(9):1298-303.

PMID:
14527352
20.

Isolation and analysis of DNA markers specific to human chromosome 15.

Tasset DM, Hartz JA, Kao FT.

Am J Hum Genet. 1988 Jun;42(6):854-66.

Supplemental Content

Support Center