SCOPUS 정보 검색 플랫폼

Volumn 59, Issue 6, 1996, Pages 1337-1342

A translocation at 12q2 refines the interval containing the Holt-Oram syndrome 1 gene

(11) Terrett, Jonathan A b Newbury Ecob, Ruth b Smith, Nigel M b Li, Quan Yi b Garrett, Christine b Cox, Phil b Bonnet, Damien b Lyonnet, Stanislas b Munnich, Arnold b Buckler, Alan J b David Brook, J a

a UNIVERSITY OF NOTTINGHAM (United Kingdom)

b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 12Q; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION 12; CYTOGENETICS; FLUORESCENCE IN SITU HYBRIDIZATION; GENE MAPPING; HOLT ORAM SYNDROME; HUMAN; MULTIPLE MALFORMATION SYNDROME; PRIORITY JOURNAL;

ARM; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 12; FEMALE; HEART DEFECTS, CONGENITAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; PHENOTYPE; SYNDROME; TRANSLOCATION, GENETIC;

EID: 19244362469 PISSN: 00029297 EISSN: None Source Type: Journal
DOI: None Document Type: Article

Times cited : (7)

References (6)

1
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- A gene for ulnar-mammary syndrome maps to 12q23-q24.1
- Bamshad M, Krakowiak PA, Watkins WS, Root S, Carey JC, Jorde LB (1995) A gene for ulnar-mammary syndrome maps to 12q23-q24.1. Hum Mol Genet 4:1973-1977
- (1995) Hum Mol Genet , vol.4 , pp. 1973-1977
- Bamshad, M.¹ Krakowiak, P.A.² Watkins, W.S.³ Root, S.⁴ Carey, J.C.⁵ Jorde, L.B.⁶

2
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- A rapid alkaline extraction procedure for screening recombinant plasmid DNA
- Birnboim HC, Doly J (1979) A rapid alkaline extraction procedure for screening recombinant plasmid DNA. Nucleic Acids Res 7:1513
- (1979) Nucleic Acids Res , vol.7 , pp. 1513
- Birnboim, H.C.¹ Doly, J.²

3
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- Genetic heterogeneity of heart-hand syndromes
- Basson CT, Solomon SD, Weissman B, MacRae CA, Poznanski AK, Prieto F, Ruiz de la Fuente WE, et al (1995) Genetic heterogeneity of heart-hand syndromes. Circulation 91:1326-1329
- (1995) Circulation , vol.91 , pp. 1326-1329
- Basson, C.T.¹ Solomon, S.D.² Weissman, B.³ MacRae, C.A.⁴ Poznanski, A.K.⁵ Prieto, F.⁶ Ruiz De La Fuente, W.E.⁷

4
- 0028264450
- A gene for Holt-Oram syndrome maps to the distal long arm of chromosome 12
- Bonnet D, Pelet A, Legeai-Mallet L, Sidi D, Mathieu M, Parent P, Plauchu H, et al (1994) A gene for Holt-Oram syndrome maps to the distal long arm of chromosome 12. Nat Genet 6:405-408
- (1994) Nat Genet , vol.6 , pp. 405-408
- Bonnet, D.¹ Pelet, A.² Legeai-Mallet, L.³ Sidi, D.⁴ Mathieu, M.⁵ Parent, P.⁶ Plauchu, H.⁷

5
- 0026314693
- Generation and fluorescent in situ hybridization mapping of yeast artificial chromosomes of 1p, 17p, 17q, and 19q from a hybrid cell-line by high-density screening of an amplified library
- Driesen MS, Dauwerse JG, Wapenaar MC, Meershoek EJ, Mollevanger P, Chen KL, Fischbeck KH, et al (1991) Generation and fluorescent in situ hybridization mapping of yeast artificial chromosomes of 1p, 17p, 17q, and 19q from a hybrid cell-line by high-density screening of an amplified library. Genomics 11:1079-1087
- (1991) Genomics , vol.11 , pp. 1079-1087
- Driesen, M.S.¹ Dauwerse, J.G.² Wapenaar, M.C.³ Meershoek, E.J.⁴ Mollevanger, P.⁵ Chen, K.L.⁶ Fischbeck, K.H.⁷

6
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- Campomelic dysplasia and autosomal sex reversal caused by mutation in an SRY-related gene
- Foster JW, Dominguez-Steglich MA, Guioli S, Kwok C, Weller PA, Stevanovic M, Weissenbach J, et al (1994) Campomelic dysplasia and autosomal sex reversal caused by mutation in an SRY-related gene. Nature 372:525-530
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.