Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome

1985 ◽  
Vol 71 (3) ◽  
pp. 211-214 ◽  
Author(s):  
Liesbeth M. Bleeker-Wagemakers ◽  
Ursula Friedrich ◽  
A. Gal ◽  
T. F. Wienker ◽  
Mette Warburg ◽  
...  
Keyword(s):  
Dna Sequence ◽  
X Chromosome ◽  
Close Linkage ◽  
Norrie Disease

scholarly journals Analysis of X chromosome genomic DNA sequence copy number variation associated with premature ovarian failure (POF)

2010 ◽  
Vol 25 (8) ◽  
pp. 2139-2150 ◽  
Author(s):  
C. R. Quilter ◽  
A. C. Karcanias ◽  
M. R. Bagga ◽  
S. Duncan ◽  
A. Murray ◽  
...  
Keyword(s):  
Copy Number Variation ◽  
Dna Sequence ◽  
X Chromosome ◽  
Premature Ovarian Failure ◽  
Copy Number ◽  
Genomic Dna ◽  
Ovarian Failure ◽  
Number Variation ◽  
Genomic Dna Sequence

Microdeletion in the X-Chromosome and Prenatal Diagnosis in a Family With Norrie Disease

Retina ◽  
1990 ◽  
Vol 10 (3) ◽  
pp. 227
Author(s):  
D P Zhu ◽  
S E Antonarakis ◽  
B J Schmeckpeper ◽  
P J Diergaarde ◽  
A E Greb ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
X Chromosome ◽  
Norrie Disease

scholarly journals Evidence of Influence of Genomic DNA Sequence on Human X Chromosome Inactivation

2006 ◽  
Vol 2 (9) ◽  
pp. e113 ◽  
Author(s):  
Zhong Wang ◽  
Huntington F Willard ◽  
Sayan Mukherjee ◽  
Terrence S Furey
Keyword(s):  
Dna Sequence ◽  
X Chromosome ◽  
Genomic Dna ◽  
X Chromosome Inactivation ◽  
Chromosome Inactivation ◽  
Genomic Dna Sequence

Nome's disease: close linkage with genetic markers from the proximal short arm of the X chromosome

2008 ◽  
Vol 27 (3) ◽  
pp. 282-283 ◽  
Author(s):  
Andreas Gal ◽  
Christine Stolzenberger ◽  
Thomas Wienker ◽  
Peter Wieacker ◽  
Hans-Hilger Ropers ◽  
...  
Keyword(s):  
Genetic Markers ◽  
X Chromosome ◽  
Close Linkage

DNA sequence variation in a non-coding region of low recombination on the human X chromosome

10.1038/8785 ◽  
1999 ◽  
Vol 22 (1) ◽  
pp. 78-81 ◽  
Author(s):  
Henrik Kaessmann ◽  
Florian Heißig ◽  
Arndt von Haeseler ◽  
Svante Pääbo
Keyword(s):  
Dna Sequence ◽  
X Chromosome ◽  
Sequence Variation ◽  
Coding Region ◽  
Dna Sequence Variation

Microdeletion in the X-Chromosome and Prenatal Diagnosis in a Family With Norrie Disease

Retina ◽  
1990 ◽  
Vol 10 (3) ◽  
pp. 227
Author(s):  
D P Zhu ◽  
S E Antonarakis ◽  
B J Schmeckpeper ◽  
P J Diergaarde ◽  
A E Greb ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
X Chromosome ◽  
Norrie Disease

Close linkage between RNR and GPD genes on the tammar wallaby (Macropus eugenii) X chromosome

1996 ◽  
Vol 72 (2-3) ◽  
pp. 197-199 ◽  
Author(s):  
L.M. McKenzie ◽  
P.G. Johnston ◽  
M.D.B. Eldridge ◽  
D.W. Cooper
Keyword(s):  
X Chromosome ◽  
Tammar Wallaby ◽  
Close Linkage ◽  
Macropus Eugenii

DNA sequence variation on the X chromosome of humans and great apes

2001 ◽  
Vol 49 (5) ◽  
pp. 394
Author(s):  
H. Kaessmann ◽  
F. Heissig ◽  
V. Wiebe ◽  
A. von Haeseler ◽  
S. Paabo
Keyword(s):  
Dna Sequence ◽  
X Chromosome ◽  
Sequence Variation ◽  
Great Apes ◽  
Dna Sequence Variation
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