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S.O.S. - BiblioFile
Prime references
A collection of nearly 30,000 prime reprints
Prader Willi Syndrome - PWS
(Searches can be focused narrowly: eg PWS)
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Last Search run on 21 Mar 2000, at 9:42am
Contains 130 references
Full bibliographies are emailed by request 

10 "Oldest" Classic References

53291. Spencer,DA (1968): Prader-Willi syndrome. Lancet 2(7 Sept), 571.

71905. Ridler,MAC; Garrod,O; Berg,JM (1971): A case of Prader-Willi syndrome in a girl with a small extra chromosome. Acta Paediatr. Scand. 60, 222-226.

1842. Hall,BD; Smith,DW (1972): Prader-Willi syndrome. A resume of 32 cases including a instance of affected first cousins, one of whom is of normal stature and intelligence. J. Pediatr. 81(2), 286-293.

71915. Hawkey,CJ; Smithies,A (1976): The Prader-Willi syndrome with a 15/15 translocation. Case report and review of the literature. J. Med. Genet. 13, 152-163.

1841. Bistrian,BR; Blackburn,GL; Stanbury,JB (1977): Metabolic aspects of a protein-sparing modified fast in the dietary management of Prader-Willi obesity. N. Engl. J. Med. 296, 774-779.

71906. Emberger,JM; Rodiere,M; Astruc,J; Brunel,D (1977): Syndrome de Prader-Willi et translocation 15-15. Ann. Genet. 20(4), 297-300.

71908. Fraccaro,M; Zuffardi,O (1977): 15,15 translocation in Prader-Willi. J. Med. Genet. 14, 275-278.

20816. Koch,G (1977): Hautleisten und krankheiten. Walter Hirsch zum Gedachtnis 1989-1974.

1666. Gorlin,RJ (1979): Risk of recurrence in usually nongenetic malformation syndromes. Birth Defects 15(5C), 181-188.

71909. Michaelsen,KF; Lundsteen,C; Hansen,FJ (1979): Prader-Willi syndrome and chromosomal mosaicism 46,XY/47,XY+mar in two cases. Clin. Genet. 16, 147-150.

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15554. Bassali,R; Hoffman,WH; Chen,H; Tuck-Muller-CM (1997): Hyperlipidemia, Insulin-Dependent Diabetes Mellitus, and Rapidly Progressive Diabetic Retinopathy and Nephropathy in Prader-Willi Syndrome with Del(15)(q11.2q13). Am. J. Med. Genet. 71, 267-270.

3770. Hall,JG (1997): Genomic Imprinting: Nature and Clinical Relevance. Annu. Rev. Med. 48, 35-44.

11634. Lalande,M (1997): Parental imprinting and human disease. Annual Review of Genetics 30, 173-195.

18418. Monaghan,KG; Van Dyke,DL; Feldman,G; Wiktor,A; Weiss,L (1997): Diagnostic testing: a cost analysis for Prader-Willi and Angelman syndromes. Am. J. Hum. Genet. 60, 244-247.

21623. Fernhoff,PM (1996): Abstracts for the Ninth Annual Scientific Conference of the Prader-Willi Syndrome (PWS) Association. Am. J. Med. Genet. 62, 205-212.

21400. Greenberg,F (1996): Contiguous gene syndromes. From Growth, Genetics, and Hormones. No reference information available.

12196. Malcom,S (1996): Microdeletion and microduplication syndromes. Prenat. Diagn. 16, 1213-1219.

16853. Smith,A (1996): Why is there no diploid overdose effect in Prader-Willi syndrome due to uniparental disomy? Acta. Genet. Med. Gemellol. Roma 45, 179-189.

16344. Chen,H; Aiello,F (1993): Trimethylaminuria in a girl with Prader-Willi syndrome and del(15)(q11q13). Am. J. Med. Genet. 45, 335-339.

17422. Coppes,MJ; Sohl,H; Teshima,IE; Mutirangura,A; Ledbetter,DH; Weksberg,R (1993): Wilms tumor in a patient with Prader-Willi syndrome. J. Pediatr. 122, 730-733.

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IBIS:International Birth Defects Information Systems

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