SCOPUS 정보 검색 플랫폼

1
- 0017260992
- Incontinentia pigmenti
- Carney RG: Incontinentia pigmenti. Arch Dermatol 1976;112:535-542.
- (1976) Arch Dermatol , vol.112 , pp. 535-542
- Carney, R.G.¹

2
- 0027403249
- Incontinentia pigmenti (Bloch-Sulzberger syndrome)
- Landy SJ, Donnai D: Incontinentia pigmenti (Bloch-Sulzberger syndrome). J Med Genet 1993;30:53-59.
- (1993) J Med Genet , vol.30 , pp. 53-59
- Landy, S.J.¹ Donnai, D.²

3
- 0023755310
- The gene for incontinentia pigmenti: Failure of linkage studies using DNA probes to confirm cytogenetic localization
- Harris A, Lankester S, Haan E, Beres J, Kulten M, Szollar J, Soutterr L, Bobrow M: The gene for incontinentia pigmenti: Failure of linkage studies using DNA probes to confirm cytogenetic localization. Clin Genet 1988;34:1-6.
- (1988) Clin Genet , vol.34 , pp. 1-6
- Harris, A.¹ Lankester, S.² Haan, E.³ Beres, J.⁴ Kulten, M.⁵ Szollar, J.⁶ Soutterr, L.⁷ Bobrow, M.⁸

4
- 0023691591
- Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11
- Sefiani A, Sinnet D, Abel L, Szpiro-Tapia S, Heuertz S, Craig I, Fraser N, Kruse TA, Frydman M, Peter MO, Schnutz JL, Gilgenkrantz S, Mitchell G, Frézal J, Melançon S: Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11. Hum Genet 1988;80:282-286.
- (1988) Hum Genet , vol.80 , pp. 282-286
- Sefiani, A.¹ Sinnet, D.² Abel, L.³ Szpiro-Tapia, S.⁴ Heuertz, S.⁵ Craig, I.⁶ Fraser, N.⁷ Kruse, T.A.⁸ Frydman, M.⁹ Peter, M.O.¹⁰ Schnutz, J.L.¹¹ Gilgenkrantz, S.¹² Mitchell, G.¹³ Frézal, J.¹⁴ Melançon, S.¹⁵

5
- 0024651107
- The gene for incontinentia pigmenti is assigned to Xq28
- Sefiani A, Abel L, Heuertz S, Sinnett D, Lavergne L, Labuda D, Hors-Cayla MC: The gene for incontinentia pigmenti is assigned to Xq28. Genomics 1989;4:427-429.
- (1989) Genomics , vol.4 , pp. 427-429
- Sefiani, A.¹ Abel, L.² Heuertz, S.³ Sinnett, D.⁴ Lavergne, L.⁵ Labuda, D.⁶ Hors-Cayla, M.C.⁷

6
- 0026063809
- Linkage relationship between incontinentia pigmenti (IP2) and nine terminal long arm markers
- Sefiani A, M'rad R, Simard L, Vincent A, Julier C, Holvoet-Vermaut L, Heuertz S, Dahl N, Stalder JF, Peter MO, Moraine C, Maleville J, Boyer J, Oberlé I, Labuda D: Linkage relationship between incontinentia pigmenti (IP2) and nine terminal long arm markers. Hum Genet 1991;86:297-299.
- (1991) Hum Genet , vol.86 , pp. 297-299
- Sefiani, A.¹ M'rad, R.² Simard, L.³ Vincent, A.⁴ Julier, C.⁵ Holvoet-Vermaut, L.⁶ Heuertz, S.⁷ Dahl, N.⁸ Stalder, J.F.⁹ Peter, M.O.¹⁰ Moraine, C.¹¹ Maleville, J.¹² Boyer, J.¹³ Oberlé, I.¹⁴ Labuda, D.¹⁵

7
- 0028069250
- The gene for the familial form of incontinentia pigmenti (IP2) maps to the distal part of Xq28
- Smahi A, Hyden-Granskog C, Peterlin B, Vabres P, Heuertz S, Fulchignoni-Lataud MC, Dahl N, Labrune P, Marec BL, Puissan C, Taieb A, von Koskull H, Hors-Cayla MC: The gene for the familial form of incontinentia pigmenti (IP2) maps to the distal part of Xq28. Hum Mol Genet 1994;3/2:273-278.
- (1994) Hum Mol Genet , vol.3 , Issue.2 , pp. 273-278
- Smahi, A.¹ Hyden-Granskog, C.² Peterlin, B.³ Vabres, P.⁴ Heuertz, S.⁵ Fulchignoni-Lataud, M.C.⁶ Dahl, N.⁷ Labrune, P.⁸ Marec, B.L.⁹ Puissan, C.¹⁰ Taieb, A.¹¹ Von Koskull, H.¹² Hors-Cayla, M.C.¹³

8
- 0028348253
- A study of X chromosome activity in two incontinentia pigmenti families with probable linkage to Xq28
- Curtis ARJ, Lindsay S, Boyle E, Clarke A, Landy SJ, Bhattacharya SS: A study of X chromosome activity in two incontinentia pigmenti families with probable linkage to Xq28. Eur J Hum Genet 1994;2:51-58.
- (1994) Eur J Hum Genet , vol.2 , pp. 51-58
- Curtis, A.R.J.¹ Lindsay, S.² Boyle, E.³ Clarke, A.⁴ Landy, S.J.⁵ Bhattacharya, S.S.⁶

9
- 0028241952
- X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the LI gene
- Jouet M, Rosenthal A, Armstrong G, MacFarlane J, Stevenson R, Paterson J, Metzenberg A, Ionasescu V, Temple K, Kenwrick S: X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the LI gene. Nature Genet 1994;7: 402-407.
- (1994) Nature Genet , vol.7 , pp. 402-407
- Jouet, M.¹ Rosenthal, A.² Armstrong, G.³ MacFarlane, J.⁴ Stevenson, R.⁵ Paterson, J.⁶ Metzenberg, A.⁷ Ionasescu, V.⁸ Temple, K.⁹ Kenwrick, S.¹⁰

10
- 0016302483
- Estimation of the recombination fraction in human pedigrees. Efficient computation of the likelihood for human linkage studies
- Ott J: Estimation of the recombination fraction in human pedigrees. Efficient computation of the likelihood for human linkage studies. Am J Hum Genet 1974;26:588-597.
- (1974) Am J Hum Genet , vol.26 , pp. 588-597
- Ott, J.¹

11
- 0026683410
- A 1.6-Mb contig of yeast artificial chromosomes around the human factor VIII gene reveals three regions homologous to probes for the DXS115 locus and two for the DXYS64 locus
- Freije D, Schlessinger D: A 1.6-Mb contig of yeast artificial chromosomes around the human factor VIII gene reveals three regions homologous to probes for the DXS115 locus and two for the DXYS64 locus. Am J Hum Genet 1992;51:66-80.
- (1992) Am J Hum Genet , vol.51 , pp. 66-80
- Freije, D.¹ Schlessinger, D.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.