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11 in total

1. Evidence for the inactivation of an X chromosome early in the development of the human female.

Authors: B R Migeon; J F Kennedy
Journal: Am J Hum Genet Date: 1975-03 Impact factor: 11.025

2. GENETIC TESTS WITH A SEX-LINKED MARKER: GLUCOSE-6-PHOSPHATE DEHYDROGENASE.

Authors: W E NANCE
Journal: Cold Spring Harb Symp Quant Biol Date: 1964

3. Sex-linked electrophoretic difference in glucose-6-phosphate dehydrogenase.

Authors: H N KIRKMAN; E M HENDRICKSON
Journal: Am J Hum Genet Date: 1963-09 Impact factor: 11.025

4. Do sequences in Xq27.3 play a role in X inactivation?

Authors: M Schmidt
Journal: Am J Med Genet Date: 1992 Apr 15-May 1

5. Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome.

Authors: M Schmidt; A Certoma; D Du Sart; P Kalitsis; M Leversha; K Fowler; L Sheffield; I Jack; D M Danks
Journal: Hum Genet Date: 1990-03 Impact factor: 4.132

6. In search of nonrandom X inactivation: studies of the placenta from newborns heterozygous for glucose-6-phosphate dehydrogenase.

Authors: B R Migeon; T T Do
Journal: Basic Life Sci Date: 1978

7. Clonal analysis using recombinant DNA probes from the X-chromosome.

Authors: B Vogelstein; E R Fearon; S R Hamilton; A C Preisinger; H F Willard; A M Michelson; A D Riggs; S H Orkin
Journal: Cancer Res Date: 1987-09-15 Impact factor: 12.701

8. Hunter disease (mucopolysaccharidosis type II) associated with unbalanced inactivation of the X chromosomes in a karyotypically normal girl.

Authors: J T Clarke; W L Greer; P M Strasberg; R D Pearce; M A Skomorowski; P N Ray
Journal: Am J Hum Genet Date: 1991-08 Impact factor: 11.025

9. Late replication in an X-autosome translocation in the mouse: correlation with genetic inactivation and evidence for selective effects during embryogenesis.

Authors: C M Disteche; E M Eicher; S A Latt
Journal: Proc Natl Acad Sci U S A Date: 1979-10 Impact factor: 11.205

10. Random X inactivation resulting in mosaic nullisomy of region Xp21.1----p21.3 associated with heterozygosity for ornithine transcarbamylase deficiency and for chronic granulomatous disease.

Authors: U Francke
Journal: Cytogenet Cell Genet Date: 1984

3 in total

1. Heritability of X chromosome--inactivation phenotype in a large family.

Authors: A K Naumova; R M Plenge; L M Bird; M Leppert; K Morgan; H F Willard; C Sapienza
Journal: Am J Hum Genet Date: 1996-06 Impact factor: 11.025

2. Myotubular myopathy in a girl with a deletion at Xq27-q28 and unbalanced X inactivation assigns the MTM1 gene to a 600-kb region.

Authors: N Dahl; L J Hu; M Chery; M Fardeau; S Gilgenkrantz; A Nivelon-Chevallier; I Sidaner-Noisette; F Mugneret; J B Gouyon; A Gal
Journal: Am J Hum Genet Date: 1995-05 Impact factor: 11.025

3. X chromosome inactivation in carriers of Barth syndrome.

Authors: K H Orstavik; R E Orstavik; A K Naumova; P D'Adamo; A Gedeon; P A Bolhuis; P G Barth; D Toniolo
Journal: Am J Hum Genet Date: 1998-11 Impact factor: 11.025

3 in total