113 related articles for article (PubMed ID: 1683160)
1. DNA deletion and its parental origin in Angelman syndrome patients.
Hamabe J; Kuroki Y; Imaizumi K; Sugimoto T; Fukushima Y; Yamaguchi A; Izumikawa Y; Niikawa N
Am J Med Genet; 1991 Oct; 41(1):64-8. PubMed ID: 1683160
[TBL] [Abstract][Full Text] [Related]
2. Molecular study of the Prader-Willi syndrome: deletion, RFLP, and phenotype analyses of 50 patients.
Hamabe J; Fukushima Y; Harada N; Abe K; Matsuo N; Nagai T; Yoshioka A; Tonoki H; Tsukino R; Niikawa N
Am J Med Genet; 1991 Oct; 41(1):54-63. PubMed ID: 1683159
[TBL] [Abstract][Full Text] [Related]
3. Detection of molecular rearrangements in Prader-Willi syndrome patients by using genomic probes recognizing four loci within the PWCR.
Gregory CA; Kirkilionis AJ; Greenberg CR; Chudley AE; Hamerton JL
Am J Med Genet; 1990 Apr; 35(4):536-45. PubMed ID: 1970703
[TBL] [Abstract][Full Text] [Related]
4. Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion.
Knoll JH; Nicholls RD; Magenis RE; Graham JM; Lalande M; Latt SA
Am J Med Genet; 1989 Feb; 32(2):285-90. PubMed ID: 2564739
[TBL] [Abstract][Full Text] [Related]
5. Molecular and clinical overlap of Angelman and Prader-Willi syndrome phenotypes.
Kirkilionis AJ; Chudley AE; Gregory CA; Hamerton JL
Am J Med Genet; 1991 Sep; 40(4):454-9. PubMed ID: 1684091
[TBL] [Abstract][Full Text] [Related]
6. Familial Angelman syndrome with a crossover in the critical deletion region.
Nelen MR; Van der Burgt CJ; Nillesen WN; Vis A; Smeets HJ
Am J Med Genet; 1994 Sep; 52(3):352-7. PubMed ID: 7810569
[TBL] [Abstract][Full Text] [Related]
7. Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome.
Nicholls RD; Knoll JH; Glatt K; Hersh JH; Brewster TD; Graham JM; Wurster-Hill D; Wharton R; Latt SA
Am J Med Genet; 1989 May; 33(1):66-77. PubMed ID: 2568752
[TBL] [Abstract][Full Text] [Related]
8. Physical mapping studies at D15S10: implications for candidate gene identification in the Angelman syndrome/Prader-Willi syndrome chromosome region of 15q11-q13.
Woodage T; Lindeman R; Deng ZM; Fimmel A; Smith A; Trent RJ
Genomics; 1994 Jan; 19(1):170-2. PubMed ID: 8188222
[TBL] [Abstract][Full Text] [Related]
9. Molecular and clinical study of 61 Angelman syndrome patients.
Saitoh S; Harada N; Jinno Y; Hashimoto K; Imaizumi K; Kuroki Y; Fukushima Y; Sugimoto T; Renedo M; Wagstaff J
Am J Med Genet; 1994 Aug; 52(2):158-63. PubMed ID: 7802001
[TBL] [Abstract][Full Text] [Related]
10. Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation.
Saitoh S; Buiting K; Cassidy SB; Conroy JM; Driscoll DJ; Gabriel JM; Gillessen-Kaesbach G; Glenn CC; Greenswag LR; Horsthemke B; Kondo I; Kuwajima K; Niikawa N; Rogan PK; Schwartz S; Seip J; Williams CA; Nicholls RD
Am J Med Genet; 1997 Jan; 68(2):195-206. PubMed ID: 9028458
[TBL] [Abstract][Full Text] [Related]
11. Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting.
Williams CA; Zori RT; Stone JW; Gray BA; Cantu ES; Ostrer H
Am J Med Genet; 1990 Mar; 35(3):350-3. PubMed ID: 2309781
[TBL] [Abstract][Full Text] [Related]
12. Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome.
Clayton-Smith J; Driscoll DJ; Waters MF; Webb T; Andrews T; Malcolm S; Pembrey ME; Nicholls RD
Am J Med Genet; 1993 Oct; 47(5):683-6. PubMed ID: 8266996
[TBL] [Abstract][Full Text] [Related]
13. Deletion of small nuclear ribonucleoprotein polypeptide N (SNRPN) in Prader-Willi syndrome detected by fluorescence in situ hybridization: two sibs with the typical phenotype without a cytogenetic deletion in chromosome 15q.
Ishikawa T; Kibe T; Wada Y
Am J Med Genet; 1996 Apr; 62(4):350-2. PubMed ID: 8723064
[TBL] [Abstract][Full Text] [Related]
14. Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: specific regions, extent of deletions, parental origin, and clinical consequences.
Magenis RE; Toth-Fejel S; Allen LJ; Black M; Brown MG; Budden S; Cohen R; Friedman JM; Kalousek D; Zonana J
Am J Med Genet; 1990 Mar; 35(3):333-49. PubMed ID: 2309780
[TBL] [Abstract][Full Text] [Related]
15. Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region.
Knoll JH; Cheng SD; Lalande M
Nat Genet; 1994 Jan; 6(1):41-6. PubMed ID: 8136833
[TBL] [Abstract][Full Text] [Related]
16. Deletion involving D15S113 in a mother and son without Angelman syndrome: refinement of the Angelman syndrome critical deletion region.
Michaelis RC; Skinner SA; Lethco BA; Simensen RJ; Donlon TA; Tarleton J; Phelan MC
Am J Med Genet; 1995 Jan; 55(1):120-6. PubMed ID: 7702085
[TBL] [Abstract][Full Text] [Related]
17. [The Angelman syndrome. Does the phenotype depend on maternal inheritance?].
Lund AM
Ugeskr Laeger; 1991 Jul; 153(28):1993-8. PubMed ID: 1862581
[TBL] [Abstract][Full Text] [Related]
18. Prader-Willi syndrome: diagnostic strategy with a cytogenetic and molecular approach.
Malzac P; Moncla A; Voelckel MA; Livet MO; Girardot L; Mattei MG; Mattei JF
Neuromuscul Disord; 1993; 3(5-6):493-6. PubMed ID: 7910502
[TBL] [Abstract][Full Text] [Related]
19. Supernumerary inv dup(15) in a patient with Angelman syndrome and a deletion of 15q11-q13.
Spinner NB; Zackai E; Cheng SD; Knoll JH
Am J Med Genet; 1995 May; 57(1):61-5. PubMed ID: 7645601
[TBL] [Abstract][Full Text] [Related]
20. FISH analysis in Prader-Willi and Angelman syndrome patients.
Bettio D; Rizzi N; Giardino D; Grugni G; Briscioli V; Selicorni A; Carnevale F; Larizza L
Am J Med Genet; 1995 Mar; 56(2):224-8. PubMed ID: 7625450
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
