SCOPUS 정보 검색 플랫폼

Volumn 10, Issue 3, 2001, Pages 243-250

Maternal sex chromosome non-disjunction: Evidence for X chromosome-specific risk factors

(7) Thomas, N Simon a Ennis, Sarah b Sharp, Andrew J a Durkie, Miranda a Hassold, Terry J c Collins, Andrew R b Jacobs, Patricia A a,b

a SALISBURY DISTRICT HOSPITAL (United Kingdom)

b SOUTHAMPTON GENERAL HOSPITAL (United Kingdom)

c CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; AUTOSOME; CENTROMERE; CHROMOSOME 15; CHROMOSOME 16; CHROMOSOME 18; CHROMOSOME 21; CHROMOSOME ABERRATION; CHROMOSOME CHIASM; CONTROLLED STUDY; ERROR; EXTRACHROMOSOMAL INHERITANCE; FEMALE; GENETIC RECOMBINATION; GENOTYPE; HUMAN; HUMAN CELL; KARYOTYPE 47,XXX; KARYOTYPE 47,XXY; MAJOR CLINICAL STUDY; MALE; MATERNAL AGE; MEIOSIS; NONDISJUNCTION; PRIORITY JOURNAL; RISK FACTOR; SEX CHROMOSOME; TRISOMY; TRISOMY 21; X CHROMOSOME; ZYGOTE;

SQUAMATA; VARANUS OLIVACEUS;

EID: 0035253363 PISSN: 09646906 EISSN: None Source Type: Journal
DOI: 10.1093/hmg/10.3.243 Document Type: Article

Times cited : (61)

References (25)

1
- 0021667423
- Trisomy in man
- (1984) Annu. Rev. Genet. , vol.18 , pp. 69-97
- Hassold, T.J.¹ Jacobs, P.A.²

2
- 0023682678
- Klinefelter's syndrome: An analysis of the origin of the additional sex chromosome using molecular probes
- (1988) Ann. Hum. Genet. , vol.52 , pp. 93-109
- Jacobs, P.A.¹ Hassold, T.J.² Whittington, E.³ Butler, G.⁴ Collyer, S.⁵ Keston, M.⁶ Lee, M.⁷

3
- 0026705388
- Reduced recombination and paternal age effect in Klinefelter syndrome
- (1992) Hum. Genet. , vol.89 , pp. 524-530
- Lorda-Sanchez, I.¹ Binkert, F.² Maechler, M.³ Robinson, W.P.⁴ Schinzel, A.A.⁵

4
- 0031961737
- Nondisjunction in the human male
- (1998) Curr. Top. Dev. Biol. , vol.37 , pp. 383-404
- Hassold, T.J.¹

5
- 6844265590
- Non-disjunction of chromosome 18
- (1998) Hum. Mol. Genet. , vol.7 , pp. 661-669
- Bugge, M.¹ Collins, A.² Petersen, M.B.³ Fisher, J.⁴ Brandt, C.⁵ Hertz, J.M.⁶ Tranebjaerg, L.⁷ Lozier-Blanchet, C.⁸ Nicolaides, P.⁹ Brondum-Nielsen, K.¹⁰

6
- 0027980592
- Non-disjunction of chromosome 21 in maternal meiosis I: Evidence for a maternal age-dependent mechanism involving reduced recombination
- (1994) Hum. Mol. Genet. , vol.3 , pp. 1529-1535
- Sherman, S.L.¹ Petersen, M.B.² Freeman, S.B.³ Hersey, J.⁴ Pettay, D.⁵ Taft, L.⁶ Frantzen, M.⁷ Mikkelsen, M.⁸ Hassold, T.J.⁹

7
- 10544226872
- Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II
- (1996) Nature Genet. , vol.14 , pp. 400-405
- Lamb, N.E.¹ Freeman, S.B.² Savage-Austin, A.³ Pettay, D.⁴ Taft, L.⁵ Hersey, J.⁶ Gu, Y.⁷ Shen, J.⁸ Saker, D.⁹ May, K.M.¹⁰

8
- 0029118422
- Recombination and maternal age-dependent nondisjunction studies of trisomy 16
- (1995) Am. J. Hum. Genet. , vol.75 , pp. 867-874
- Hassold, T.¹ Merrill, M.² Adkins, K.³ Freeman, S.⁴ Sherman, S.⁵

9
- 7144260410
- Maternal meiosis I non-disjunction of chromosome 15: Dependence of the maternal age effect on the level of recombination
- (1998) Hum. Mol. Genet. , vol.7 , pp. 1011-1019
- Robinson, W.P.¹ Kuchinka, B.D.² Bernasconi, F.³ Petersen, M.B.⁴ Schulze, A.⁵ Brondum-Nielsen, K.⁶ Christian, S.L.⁷ Ledbetter, D.H.⁸ Schinzel, A.A.⁹ Horsthemke, B.¹⁰

10
- 0028030585
- The origin of 47,XXY and 47,XXX aneuploidy: Heterogeneous mechanisms and role of aberrant recombination
- (1994) Hum. Mol. Genet. , vol.3 , pp. 1365-1371
- MacDonald, M.¹ Hassold, T.² Harvey, J.³ Wang, L.H.⁴ Morton, N.E.⁵ Jacobs, P.⁶

11
- 0030586894
- Linkage map integration
- (1996) Genomics , vol.46 , pp. 157-162
- Collins, A.¹ Teague, J.² Keats, B.J.³ Morton, N.E.⁴

12
- 0033777149
- A reinvestigation of non-disjunction resulting in 47,XXY males of paternal origin
- (2000) Eur. J. Hum. Genet. , vol.8 , pp. 805-808
- Thomas, N.S.¹ Collins, A.R.² Hassold, T.J.³ Jacobs, P.A.⁴

13
- 0026334334
- XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region
- (1991) Am. J. Hum. Genet. , vol.49 , pp. 254-260
- Hassold, T.J.¹ Sherman, S.L.² Pettay, D.³ Page, D.C.⁴ Jacobs, P.A.⁵

14
- 0006295027
- Methods in Genetic Epidemiology. Karger, Basel, Switzerland.
- (1983)
- Morton, N.E.¹ Rao, D.C.² Lalouel, J.-M.³

15
- 0026000975
- Trisomy 21: Association between reduced recombination and nondisjunction
- (1991) Am. J. Hum. Genet. , vol.49 , pp. 608-620
- Sherman, S.L.¹ Takaesu, N.² Freeman, S.B.³ Grantham, M.⁴ Phillips, C.⁵ Blackston, R.D.⁶ Jacobs, P.A.⁷ Cockwell, A.E.⁸ Freeman, V.⁹ Uchida, I.¹⁰

16
- 9844220844
- Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21
- (1997) Hum. Mol. Genet. , vol.6 , pp. 1391-1399
- Lamb, N.E.¹ Feingold, E.² Savage, A.³ Avramopoulos, D.⁴ Freeman, S.⁵ Gu, Y.⁶ Hallberg, A.⁷ Hersey, J.⁸ Karadima, G.⁹ Pettay, D.¹⁰

17
- 0031911344
- Physical and genetic mapping of the human X chromosome centromere: Repression of recombination
- (1998) Genome Res. , vol.8 , pp. 100-110
- Mahtani, M.M.¹ Willard, H.F.²

18
- 0029852774
- (1996) Nature Genet. , vol.14 , pp. 406-414
- Koehler, K.E.¹ Boulton, C.L.² Collins, H.E.³ French, R.L.⁴ Herman, K.C.⁵ Lacefield, S.M.⁶ Madden, L.D.⁷ Schuetz, C.D.⁸ Hawley, R.S.⁹

19
- 0030884929
- Human centromeric DNAs
- (1997) Hum. Genet. , vol.100 , pp. 291-304
- Lee, C.¹ Wevrick, R.² Fisher, R.B.³ Ferguson-Smith, M.M.⁴ Lin, C.C.⁵

20
- 0027447719
- Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age
- (1993) Nature Genet. , vol.3 , pp. 146-150
- Antonarakis, S.E.¹ Avramopoulos, D.² Blouin, J.-L.³ Talbot, C.C.⁴ Schinzel, A.A.⁵

21
- 0030064773
- Trisomy of human chromosome 18: Molecular studies on parental origin and cell stage of nondisjunction
- (1996) Hum. Genet. , vol.97 , pp. 218-223
- Eggermann, T.¹ Nothen, M.M.² Eiben, B.³ Hofmann, D.⁴ Hinkel, K.⁵ Fimmers, R.⁶ Schwanitz, G.⁷

22
- 0028907505
- Trisomy 18: Studies of the parent and cell division of origin and the effect of aberrant recombination on nondisjunction
- (1995) Am. J. Hum. Genet. , vol.56 , pp. 669-675
- Fisher, J.M.¹ Harvey, J.F.² Morton, N.E.³ Jacobs, P.A.⁴

23
- 0025020073
- A centromere map of the X chromosome from trisomies of maternal origin
- (1990) Am. Hum. Genet. , vol.54 , pp. 39-47
- Morton, N.E.¹ Keats, B.J.² Jacobs, P.A.³ Hassold, T.⁴ Pettay, D.⁵ Harvey, J.⁶ Andrews, V.⁷

24
- 14444286943
- X chromosome map at 75-Kb STS resolution, revealing extremes of recombination and GC content
- (1997) Genome Res. , vol.7 , pp. 210-222
- Nagaraja, R.¹ MacMillan, S.² Kere, J.³ Jones, C.⁴ Griffin, S.⁵ Schmatz, M.⁶ Terrell, J.⁷ Shomaker, M.⁸ Jermak, C.⁹ Hott, C.¹⁰

25
- 0028198384
- The sequence organization of the long arm pseudoautosomal region of the human sex chromosomes
- (1994) Hum. Mol. Genet. , vol.3 , pp. 771-778
- Kvaloy, K.¹ Galvagni, F.² Brown, W.R.A.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.