//wimprinting and syndrome
IMPRINTING AND SYNDROME matched 17 items.
1 Schachter, M. (Neurology. ... 05/01/95)
Clinical evidence of genomic imprinting in Tourette'... **FAX 1HR*
2 Stoll, C. (Annales de genetique. 1995 )
No evidence for genomic imprinting in liveborn Down
3 Choen, Jr. M. Michae (American journal of medical genet... 08/15/94)
Letter to the Editor: Wiedemann-Beckwith Syndrome, I...
4 Weksberg, Rosanna (American journal of medical genet... 08/15/94)
Letter to the Editor: Wiedemann-Beckwith Syndrome: G...
5 Furtado, Sarah (American journal of medical genet... 05/15/94)
Investigation of the Potential Role of Genetic Impri...
6 Reed, M. L. (Nature genetics. ... 02/01/94)
Maternal imprinting of human SNRPN, a gene deleted i...
7 Weksberg, R. (Nature genetics. 10/01/93)
Disruption of insulin-like growth factor 2 imprintin...
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AUTHOR(s): Furtado, Sarah
Suchowersky, Oksana
TITLE(s): Investigation of the Potential Role of Genetic Imprinting
in Gilles de la Tourette Syndrome.
In: American journal of medical genetics.
MAY 15 1994 v 51 n 1
Page: 51
SICI Code: 0148-7299(19940515)51:1L.51:IPRG;1-
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AUTHOR(s): Reed, M. L.
Leff, S. E.
TITLE(s): Maternal imprinting of human SNRPN, a gene deleted in
Prader-Willi syndrome.
In: Nature genetics.
FEB 01 1994 v 6 n 2
Page: 163
SICI Code: 1061-4036(19940201)6:2L.163:MIHS;1-
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AUTHOR(s): Weksberg, R.
Shen, D.R.
Fei, Y.L.
TITLE(s): Disruption of insulin-like growth factor 2 imprinting in
Beckwith-Wiedemann syndrome.
In: Nature genetics.
OCT 01 1993 v 5 n 2
Page: 143
8 Meijers-Heijboer, E. (Journal of medical genetics. 12/01/92)
Linkage analysis with chromosome 15q11-13 markers sh...
9 Leff, S. E. (Nature genetics. 12/01/92)
Maternal imprinting of the mouse Snrpn gene and cons...
10 Junien, Claudine (Current opinion in genetics & dev... 06/01/92)
Beckwith-Wiedemann syndrome, tumourigenesis and impr...
11 Viljoen, D. (Journal of medical genetics. 04/01/92)
Evidence for paternal imprinting in familial Beckwit...
12 Gregory, C.A. (Human genetics. ... 11/01/91)
Somatic recombination rather than uniparental disomy... **FAX 1HR*
13 Laird, Charles D. (The American journal of human gen... 04/01/90)
Two Progenitor Cells for Human Oogonia Inferred from...
14 Khalifa, Mohamed M. (The American journal of human gen... 04/01/90)
Methylation Status of Genes Flanking the Fragile Sit...
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AUTHOR(s): Meijers-Heijboer, E.J.
Sandkuijl, L.A.
Brunner, H.G.
TITLE(s): Linkage analysis with chromosome 15q11-13 markers shows
genomic imprinting in familial Angelman syndrome.
In: Journal of medical genetics.
DEC 01 1992 v 29 n 12
Page: 853
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AUTHOR(s): Leff, S. E.
Brannan, C. I.
Reed, M. L.
TITLE(s): Maternal imprinting of the mouse Snrpn gene and conserved
linkage homology with the human Prader-Willi syndrome.
In: Nature genetics.
DEC 01 1992 v 2 n 4
Page: 259
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AUTHOR(s): Gregory, C.A.
Schwartz, J.
Kirkilionis, A.J.
TITLE(s): Somatic recombination rather than uniparental disomy
suggested as another mechanism by which genetic imprinting
may play a role in the etiology of Prader-Willi syndrome.
In: Human genetics.
NOV 01 1991 v 88 n 1
Page: 42
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AUTHOR(s): Laird, Charles D.
Lamb, Mary M.
Thorne, Jeffrey L.
TITLE(s): Two Progenitor Cells for Human Oogonia Inferred from
Pedigree Data and the X-Inactivation Imprinting Model of
the Fragile-X Syndrome.
In: American journal of human genetics.
APR 01 1990 v 46 n 4
Page: 696
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AUTHOR(s): Khalifa, Mohamed M.
Reiss, Allan L.
Migeon, Barbara R.
TITLE(s): Methylation Status of Genes Flanking the Fragile Site in
Males with the Fragile-X Syndrome: A Test of the Imprinting
Hypothesis.
In: American journal of human genetics.
APR 01 1990 v 46 n 4
Page: 744
15 Sved, John A. (American journal of human genetics. 03/01/90)
Population Genetic Consequences of the Fragile-X Syn...
16 Williams, C. A. (American journal of medical genet... 03/01/90)
Maternal Origin of 15q11-13 Deletions in Angelman Sy...
17 Laird, Charles D. (The Nucleus. 04/01/89)
Chromosomal imprinting in the fragile X syndrome.
//wmethylation and imprinting
METHYLATION AND IMPRINTING matched 17 items.
1 Ariel, M. (Nature genetics. ... 03/01/95)
Gamete-specific methylation correlates with imprinti...
2 Takahashi, Y. (Chromosoma. 12/01/94)
Methylation imprinting was observed of mouse mo-2 ma...
3 Rainer, S. (Journal of the National Cancer In... 07/06/94)
Erratum: Genomic Imprinting, DNA Methylation, and Ca...
4 Steenman, M.J.C. (Nature genetics. ... 07/01/94)
Loss of imprinting of IGF2 is linked to reduced expr...
5 Razin, A. (Cell. 05/20/94)
DNA Methylation and Genomic Imprinting.
6 Rainier, S. (Journal of the National Cancer In... 05/18/94)
Genomic Imprinting, DNA Methylation, and Cancer.
7 Reis, Andre (American journal of human genetics. 05/01/94)
Imprinting Mutations Suggested by Abnormal DNA Methy...
8 Li, E. (Nature. 11/25/93)
Role for DNA methylation in genomic imprinting.
9 Zhang, Yonghui (American journal of human genetics. 07/01/93)
Imprinting of Human H10: Allele-specific CpG Methyla...
10 Stoger, R. (Cell. 04/09/93)
Maternal-Specific Methylation of the imprinted mouse...
11 Sasaki, H. (Development. 02/01/91)
Inherited type of allelic methylation variations in
12 Driscoll, Daniel J. (Somatic cell and molecular geneti... 05/01/90)
Sex Difference in Methylation of Single-Copy genes i... **FAX 1HR*
13 Khalifa, Mohamed M. (The American journal of human gen... 04/01/90)
Methylation Status of Genes Flanking the Fragile Sit...
14 Monk, Marilyn (Philosophical transactions of the... 01/30/90)
Changes in DNA methylation during mouse embryonic de...
15 Surani, M. A. (Philosophical transactions of the... 01/30/90)
Developmental consequences of imprinting of parental...
16 Sapienza, C. (Development. 09/01/89)
Epigenetic and genetic factors affect transgene meth...
17 Collick, A. (Development. 10/01/88)
CpG methylation of an X-linked transgene is determin...
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AUTHOR(s): Surani, M. A.
Allen, N. D.
Barton, S. C.
TITLE(s): Developmental consequences of imprinting of parental
chromosomes by DNA methylation.
In: Philosophical transactions of the royal society
JAN 30 1990 v 326 n 1235
Page: 313