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Genome Research

Volumn 11, Issue 6, 2001, Pages 1086-1094

Sequence-based design of single-copy genomic DNA probes for fluorescence in situ hybridization

(3) Rogan, P K a Cazcarro, P M a Knoll, J H M a

a UNIVERSITY OF MISSOURI KANSAS CITY (United States)

Author keywords

[No Author keywords available]

Indexed keywords

REPETITIVE DNA;

ARTICLE; CALCULATION; CHROMOSOME 15Q; CHROMOSOME 1P; CHROMOSOME 21; CHROMOSOME 22; CHROMOSOME 22Q; CHROMOSOME REARRANGEMENT; CONTROLLED STUDY; DNA HYBRIDIZATION; DNA PROBE; DNA PURIFICATION; DNA RECOMBINATION; DNA SEQUENCE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE LOCUS; GENETIC DISTANCE; HUMAN; METAPHASE; MONITORING; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

BASE SEQUENCE; CHROMOSOMES, HUMAN, PAIR 21; CHROMOSOMES, HUMAN, PAIR 22; DNA PROBES; GENE DOSAGE; GENOME, HUMAN; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; NUCLEIC ACID HYBRIDIZATION; RESEARCH DESIGN; SEQUENCE ANALYSIS, DNA;

EID: 0034837436 PISSN: 10889051 EISSN: None Source Type: Journal
DOI: 10.1101/gr.171701 Document Type: Article

Times cited : (31)

References (28)

1
- 0025183708
- Basic local alignment search tool
- (1990) J. Mol. Biol. , vol.215 , pp. 403-410
- Altschul, S.F.¹ Gish, W.² Miller, W.³ Myers, E.W.⁴ Lipman, D.J.⁵

2
- 0030008257
- Integration of the cytogenetic, genetic, and physical maps of the human genome by FISH mapping of CEPH YAC clones
- (1996) Genomics , vol.32 , pp. 1-14
- Bray-Ward, P.¹ Menninger, J.² Lieman, J.³ Desai, T.⁴ Mokady, N.⁵ Banks, A.⁶ Ward, D.C.⁷

3
- 0016991656
- DNA sequence arrangement and preliminary evidence on its evolution
- (1976) Fed. Proc. , vol.35 , pp. 2151-2157
- Britten, R.J.¹ Davidson, E.N.²

4
- 0002760686
- Nucleotide sequence repetition in DNA
- 1965. Carnegie Institution of Washington.
- (1965) Carnegie Inst. Wash. Yearbook , pp. 78-84
- Britten, R.J.¹ Kohne, D.E.²

5
- 0026688328
- Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome
- (1992) Am. J. Hum. Genet. , vol.5 , pp. 964-970
- Carey, A.H.¹ Kelly, D.² Halford, S.³ Wadey, R.⁴ Wilson, D.⁵ Goodship, J.⁶ Burn, J.⁷ Paul, T.⁸ Sharkey, A.⁹ Dumanski, J.¹⁰

6
- 0028261194
- Effective amplification of long targets from cloned inserts and human genomic DNA
- (1994) Proc. Natl. Acad. Sci. , vol.91 , pp. 5695-5699
- Cheng, S.¹ Fockler, C.² Barnes, W.M.³ Higuchi, R.⁴

7
- 0029952699
- Association of a mosaic chromosomal 22q11 deletion with hypoplastic left heart syndrome
- (1996) Am. J. Cardiol. , vol.77 , pp. 1023-1025
- Consevage, M.W.¹ Seip, J.R.² Belchis, D.A.³ Davis, A.T.⁴ Baylen, B.G.⁵ Rogan, P.K.⁶

8
- 0030954752
- Removal of repetitive sequences from FISH probes using PCR-assisted affinity chromatography
- (1997) Hum. Genet. , vol.100 , pp. 472-476
- Craig, J.M.¹ Kraus, J.² Cremer, T.³

9
- 0026750771
- A genetic etiology for DiGeorge syndrome: Consistent deletions and microdeletions of 22q11
- (1992) Am. J. Hum. Genet. , vol.50 , pp. 924-933
- Driscoll, D.A.¹ Budarf, M.L.² Emmanuel, B.S.³

10
- 79960655760
- The DNA sequence of human chromosome 22
- (1999) Nature , vol.402 , pp. 489-495
- Dunham, I.¹ Shimizu, N.² Roe, B.A.³ Chissoe, S.⁴ Hunt, A.R.⁵ Collins, J.E.⁶ Bruskiewich, R.⁷ Beare, D.M.⁸ Clamp, M.⁹ Smink, L.J.¹⁰

11
- 0025348555
- Molecular studies of DiGeorge syndrome
- (1990) Am. J. Hum. Genet. , vol.46 , pp. 888-895
- Fibison, W.J.¹ Budarf, M.² McDermid, H.³ Greenberg, F.⁴ Emanuel, B.S.⁵

12
- 0028989174
- High-resolution DNA Fiber-FISH for genomic DNA mapping and colour bar-coding of large genes
- (1995) Hum. Mol. Genet. , vol.4 , pp. 831-836
- Florijn, R.J.¹ Bonden, L.A.² Vrolijk, H.³ Wiegant, J.⁴ Vaandrager, J.W.⁵ Baa, F.⁶ Den Dunnen, J.T.⁷ Tanke, J.J.⁸ Van Ommen, G.J.⁹ Raap, A.K.¹⁰

13
- 0024695739
- An efficient method for selecting unique-sequence clones from DNA libraries and its application to fluorescent staining of human chromosome 21 using in situ hybridization
- (1989) Genomics , vol.5 , pp. 100-109
- Fuscoe, J.C.¹ Collins, C.C.² Pinkel, D.³ Gray, J.W.⁴

14
- 0029010132
- Human genome organization
- (1995) Curr. Opin. Genet. Dev. , vol.5 , pp. 315-322
- Gardiner, K.¹

15
- 0034682403
- The DNA sequence of human chromosome 21
- (2000) Nature , vol.405 , pp. 311-319
- Hattori, M.¹ Fujiyama, A.² Taylor, T.D.³ Watanabe, H.⁴ Yada, T.⁵ Park, H.-S.⁶ Toyoda, A.⁷ Ishii, K.⁸ Totoki, Y.⁹ Choi, D.-K.¹⁰

16
- 0034028921
- Structure of chromosomal duplicons and their role in mediating human genomic disorders
- (2000) Genome Res. , vol.10 , pp. 597-610
- Ji, Y.¹ Eichler, E.E.² Schwartz, S.³ Nicholls, R.D.⁴

17
- 0032103760
- Repeats in genomic DNA: Mining and meaning
- (1998) Curr. Opin. Struct. Biol. , vol.8 , pp. 333-337
- Jurka, J.¹

18
- 0030094146
- CENSOR-a program for identification and elimination of repetitive elements from DNA sequences
- (1996) Comput. Chem. , vol.20 , pp. 119-122
- Jurka, J.¹ Klonowski, P.² Dagman, V.³ Pelton, P.⁴

19
- 0024619007
- Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion
- (1989) Amer. J. Med. Genet. , vol.32 , pp. 285-290
- Knoll, J.H.¹ Nicholls, R.D.² Magenis, R.E.³ Graham, J.M.⁴ Lalande, M.⁵

20
- 0000703709
- In situ hybridization to metaphase chromosomes interphase nuclei
- unit 4.3. (eds. N.C. Dracopoli, et al), John Wiley, New York.
- (1994) Current Protocols in Human Genetics , vol.1
- Knoll, J.H.M.¹ Lichter, P.²

21
- 0032694507
- Human genome anatomy: BACs integrating the genetic and cytogenetic maps for bridging genome and biomedicine
- (1999) Genome Res. , vol.9 , pp. 994-1001
- Korenberg, J.R.¹ Chen, X.N.² Sun, Z.³ Shi, Z.Y.⁴ Ma, S.⁵ Vataru, E.⁶ Yimlamai, D.⁷ Weissenbach, J.S.⁸ Shizuya, H.⁹ Simon, M.I.¹⁰

22
- 0023692635
- Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries
- (1988) Hum. Genet. , vol.80 , pp. 224-234
- Lichter, P.¹ Cremer, T.² Borden, J.³ Manuelidis, L.⁴ Ward, D.C.⁵

23
- 0031754413
- Pathological consequences of sequence duplications in the human genome
- (1998) Genome Res. , vol.8 , pp. 1007-1021
- Mazzarella, R.¹ Schlessinger, D.²

24
- 0024397019
- Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome
- (1989) Amer. J. Med. Genet. , vol.33 , pp. 66-77
- Nicholls, R.D.¹ Knoll, J.H.² Glatt, K.³ Hersh, J.H.⁴ Brewster, T.D.⁵ Graham, J.M.⁶ Wurster-Hill, D.⁷ Wharton, R.⁸ Latt, S.A.⁹

25
- 0343319476
- Fluorescence in situ hybridization with human chromosome-specific libraries: Detection of trisomy 21 and translocations of chromosome 4
- (1988) Proc. Natl. Acad. Sci. , vol.85 , pp. 9138-9142
- Pinkel, D.¹ Landegent, J.² Collins, C.³ Fuscoe, J.⁴ Segraves, R.⁵ Lucas, J.⁶ Gray, J.⁷

26
- 0022431971
- Removal of repeated sequences from hybridization probes
- (1985) Nucl. Acids Res. , vol.13 , pp. 1905-1922
- Sealey, P.G.¹ Whittaker, P.A.² Southern, E.M.³

27
- 0032884027
- Monosomy 1p36
- (1999) J. Med. Genet. , vol.36 , pp. 657-663
- Slavotinek, A.¹ Shaffer, L.G.² Shapira, S.K.³

28
- 0027516045
- Fluorescence in situ hybridization mapping of human chromosome 19: Cytogenetic band location of 540 cosmids and 70 genes or DNA markers
- (1993) Genomics , vol.15 , pp. 133-145
- Trask, B.¹ Fertitta, A.² Christensen, M.³ Youngblom, J.⁴ Bergmann, A.⁵ Copeland, A.⁶ De Jong, P.⁷ Mohrenweiser, H.⁸ Olsen, A.⁹ Carrano, A.¹⁰

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