Similar articles for PMID: 6467659

Year	Number of Results
1969	1
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1977	5
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1983	3
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1988	2
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2012	1
2013	1
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2015	1
2017	1
2018	1
2021	1
2024	0

1

Duplication in the proximal portion of the long arm of chromosome 15, in a girl without phenotypic features of the Prader-Willi syndrome.

Veenema H, Beverstock GC, Zvelebil-Tarasevitch N, Doorn JL, van Parys JA, v d Kamp JJ. Veenema H, et al. Clin Genet. 1984 Jul;26(1):65-8. doi: 10.1111/j.1399-0004.1984.tb00791.x. Clin Genet. 1984. PMID: 6467659

2

Duplication or insertion in 15q11-13 associated with mental retardation-short stature and obesity-Prader-Willi or Cohen syndrome?

Fuhrmann-Rieger A, Köhler A, Fuhrmann W. Fuhrmann-Rieger A, et al. Clin Genet. 1984 Apr;25(4):347-52. doi: 10.1111/j.1399-0004.1984.tb02002.x. Clin Genet. 1984. PMID: 6713711

3

Duplication in chromosome 15q in a boy with the Prader-Willi syndrome; further cytogenetic confusion.

de France HF, Beemer FA, Ippel PF. de France HF, et al. Clin Genet. 1984 Oct;26(4):379-82. doi: 10.1111/j.1399-0004.1984.tb01075.x. Clin Genet. 1984. PMID: 6499252

4

Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainment.

Fraccaro M, Zuffardi O, Bühler E, Schinzel A, Simoni G, Witkowski R, Bonifaci E, Caufin D, Cignacco G, Delendi N, et al. Fraccaro M, et al. Hum Genet. 1983;64(4):388-94. doi: 10.1007/BF00292373. Hum Genet. 1983. PMID: 6618490

5

'Expanded' Prader-Willi syndrome in a boy with an unusual 15q chromosome deletion.

Pauli RM, Meisner LF, Szmanda RJ. Pauli RM, et al. Am J Dis Child. 1983 Nov;137(11):1087-9. doi: 10.1001/archpedi.1983.02140370047015. Am J Dis Child. 1983. PMID: 6637912

6

Duplication of chromosome 15 in the region 15q11-13 in a patient with developmental delay and ataxia with similarities to Angelman syndrome.

Clayton-Smith J, Webb T, Cheng XJ, Pembrey ME, Malcolm S. Clayton-Smith J, et al. J Med Genet. 1993 Jun;30(6):529-31. doi: 10.1136/jmg.30.6.529. J Med Genet. 1993. PMID: 8326502 Free PMC article. Review.

7

Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes.

Kalsner L, Chamberlain SJ. Kalsner L, et al. Pediatr Clin North Am. 2015 Jun;62(3):587-606. doi: 10.1016/j.pcl.2015.03.004. Epub 2015 Apr 22. Pediatr Clin North Am. 2015. PMID: 26022164 Free PMC article. Review.

8

Abnormal chromosome in Prader-Willi syndrome.

Goh K, Herrmann MA, Campbell RG, Thompson D. Goh K, et al. Clin Genet. 1984 Dec;26(6):597-601. doi: 10.1111/j.1399-0004.1984.tb01110.x. Clin Genet. 1984. PMID: 6499272

9

Proximal duplication of the long arm of chromosome 10 (10q11.2----10q22): a distinct clinical entity.

Fryns JP, Kleczkowska A, Igodt-Ameye L, Van den Berghe H. Fryns JP, et al. Clin Genet. 1987 Jul;32(1):61-5. doi: 10.1111/j.1399-0004.1987.tb03325.x. Clin Genet. 1987. PMID: 3502695

10

Ring chromosome 14 in a mentally retarded girl.

Iselius L, Ritzén M, Bui TH, Olsson K, Eklöf O. Iselius L, et al. Acta Paediatr Scand. 1980 Nov;69(6):803-6. doi: 10.1111/j.1651-2227.1980.tb07157.x. Acta Paediatr Scand. 1980. PMID: 7211367

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