SCOPUS 정보 검색 플랫폼

Volumn 119 A, Issue 3, 2003, Pages 400-

Comments on "Osteopathia Striata Cranial Sclerosis: Non-random X-inactivation suggestive of X-linked dominant inheritance" [4]

(3) Kraus, C b Konig R c Rott, Hans Dieter a,b

a UNIVERSITY HOSPITAL ERLANGEN (Germany)

b UNIVERSITY OF ERLANGEN NUREMBERG (Germany)

c GOETHE UNIVERSITY (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ANDROGEN RECEPTOR;

HUMAN; LETTER; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SCLEROSIS; SKULL DISEASE; X CHROMOSOME; X CHROMOSOME DOMINANT INHERITANCE; X CHROMOSOME INACTIVATION;

EID: 0042823594 PISSN: 15524825 EISSN: None Source Type: Journal
DOI: 10.1002/ajmg.a.20178 Document Type: Letter

Times cited : (2)

References (7)

1
- 0026678490
- Methylation of HpaII and HhI sites near the polymorphic CAG repeat in the human androgen receptor gene correlates with X chromosome inactivation
- Allen RC, Zoghbi HY, Moseley HB, Rosenblatt HM, Belmont JW. 1992. Methylation of HpaII and HhI sites near the polymorphic CAG repeat in the human androgen receptor gene correlates with X chromosome inactivation. Am J Hum Genet 51:1229-1239.
- (1992) Am J Hum Genet , vol.51 , pp. 1229-1239
- Allen, R.C.¹ Zoghbi, H.Y.² Moseley, H.B.³ Rosenblatt, H.M.⁴ Belmont, J.W.⁵

2
- 0030062816
- X-chromosome methylation ratios as indicators of chromosomal activity: Evidence of intraindividual divergencies among tissues of different embryonal origin
- Azofeifa J, Waldherr R, Cremer M. 1996. X-chromosome methylation ratios as indicators of chromosomal activity: Evidence of intraindividual divergencies among tissues of different embryonal origin. Hum Genet 97:330-333.
- (1996) Hum Genet , vol.97 , pp. 330-333
- Azofeifa, J.¹ Waldherr, R.² Cremer, M.³

3
- 0029873138
- Osteopathia striata with cranial sclerosis: Variable expressivity in a four generation pedigree
- König R, Dukiet C, Dörries A, Zabel B, Fuchs S. 1996. Osteopathia striata with cranial sclerosis: Variable expressivity in a four generation pedigree. Am J Med Genet 63:68-73.
- (1996) Am J Med Genet , vol.63 , pp. 68-73
- König, R.¹ Dukiet, C.² Dörries, A.³ Zabel, B.⁴ Fuchs, S.⁵

4
- 0036306870
- Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders
- Plenge RM, Stevenson RA, Lubs HA, Schwartz CE, Willard HF. 2002. Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders. Am J Hum Genet 71:168-173.
- (2002) Am J Hum Genet , vol.71 , pp. 168-173
- Plenge, R.M.¹ Stevenson, R.A.² Lubs, H.A.³ Schwartz, C.E.⁴ Willard, H.F.⁵

5
- 0141644179
- Multiple Malformations in a male and maternal osteopathia striata with cranial sclerosis
- in press
- Rott HD, Krieg P, Rütschle H, Kraus C. Multiple Malformations in a male and maternal osteopathia striata with cranial sclerosis. Genet Counsel 14:(in press).
- Genet Counsel , vol.14
- Rott, H.D.¹ Krieg, P.² Rütschle, H.³ Kraus, C.⁴

6
- 0033762221
- Age- and tissue-specific variation of X chromosome inactivation ratios in normal women
- Sharp A, Robinson D, Jacobs P. 2000. Age- and tissue-specific variation of X chromosome inactivation ratios in normal women. Hum Genet 107: 343-349.
- (2000) Hum Genet , vol.107 , pp. 343-349
- Sharp, A.¹ Robinson, D.² Jacobs, P.³

7
- 18244378307
- Osteopathia striata cranial sclerosis: Non-random X-inactivation suggestive of X-linked dominant inheritance
- Viot G, Lacombe D, David A, Mathieu M, De Broca A, Faivre L, Gigarel N, Munnich A, Lyonnet S, Le Merrer M, Cormier-Daire V. 2002. Osteopathia striata cranial sclerosis: Non-random X-inactivation suggestive of X-linked dominant inheritance. Am J Med Genet 107: 1-4.
- (2002) Am J Med Genet , vol.107 , pp. 1-4
- Viot, G.¹ Lacombe, D.² David, A.³ Mathieu, M.⁴ De Broca, A.⁵ Faivre, L.⁶ Gigarel, N.⁷ Munnich, A.⁸ Lyonnet, S.⁹ Le Merrer, M.¹⁰ Cormier-Daire, V.¹¹

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.