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1 . Academic Journal
Altered patterns of meiotic recombination in human fetal oocytes with asynapsis and/or synaptonemal complex fragmentation at pachytene
저자
by
Tease, Charles
;
Hartshorne, Geraldine
;
Hultén, Maj
.
소스
In
Reproductive BioMedicine Online
2006 13(1):88-95
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5 . Academic Journal
Radiation-Induced Chromosomal Breaks may be DNA Repair Fragile Sites with Larger-scale Correlations to Eight Double-Strand-Break Related Data Sets over the Human Genome.
저자
by
Brahme, Anders
;
Hultén, Maj
;
Bengtsson, Carin
;
Hultgren, Andreas
;
Zetterberg, Anders
.
소스
Radiation Research; Nov2019, Vol. 192 Issue 5, p562-576, 15p
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7 . Academic Journal
Combined serum and nuchal translucency screening in the first trimester achieves 85% to 90% detection rate for Down and Edward syndromes
저자
by
Hultén, Maj
.
소스
In
Evidence-based Healthcare
2004 8(2):82-84
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3 . Book
Meiosis and Meiotic Errors
저자
by
Baker, Hazel
;
Hultén, Maj
;
Tankimanova, Maira
.
소스
Encyclopedia of Genetics, Genomics, Proteomics and Bioinformatics. 2005, v. 1, p102-121.
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5 . Academic Journal
Corrigendum to “MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved region” [Brain Dev 2001; 23: S246–50]
저자
by
Vacca, Marcella
;
Filippini, Francesco
;
Budillon, Alberta
;
Rossi, Valeria
;
Ragione, Floriana Della
, et al.
소스
In
Brain and Development
November 2012 34(10):891-891
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7 . Academic Journal
Novel rare alleles of ABCA1 are exclusively associated with extreme high-density lipoprotein-cholesterol levels among the Han Chinese
저자
by
Hu, Suwei
;
Zhong, Yanfang
;
Hao, Yuantao
;
Luo, Minqi
;
Zhou, Yan
, et al.
소스
Clinical Chemistry and Laboratory Medicine (CCLM)
. 47(10):1239-1245
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7 . Academic Journal
Novel rare alleles of ABCA1 are exclusively associated with extreme high-density lipoprotein-cholesterol levels among the Han Chinese.
저자
by
Suwei Hu
;
Yanfang Zhong
;
Yuantao Hao
;
Minqi Luo
;
Yan Zhou
, et al.
소스
Clinical Chemistry & Laboratory Medicine
. Oct2009, Vol. 47 Issue 10, p1239-1245. 7p. 1 Diagram, 4 Charts, 1 Graph.
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7 . Academic Journal
Increased skewing of X chromosome inactivation in Rett syndrome patients and their mothers.
저자
by
Knudsen, Gun Peggy S.
;
Neilson, Tracey C. S.
;
Pedersen, June
;
Kerr, Alison
;
Schwartz, Marianne
, et al.
소스
European Journal of Human Genetics
. Nov2006, Vol. 14 Issue 11, p1189-1194. 6p. 1 Chart, 1 Graph.
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7 . Academic Journal
The X-linked methyl binding protein gene Kaiso is highly expressed in brain but is not mutated in Rett syndrome patients
저자
by
Della Ragione, Floriana
;
Tiunova, Anna
;
Vacca, Marcella
;
Strazzullo, Maria
;
González, Eva
, et al.
소스
Gene
. May2006, Vol. 373, p83-89. 7p.
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7 . Academic Journal
Dimensional phenotypic analysis and functional categorisation of mutations reveal novel genotype–phenotype associations in Rett syndrome.
저자
by
Charman, Tony
;
Neilson, Tracey C. S.
;
Mash, Veronica
;
Archer, Hayley
;
Gardiner, Mary T.
, et al.
소스
European Journal of Human Genetics
. Oct2005, Vol. 13 Issue 10, p1121-1130. 10p.
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