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weitere (Fach) Literatur...
Curfs, L.M.G., F.C.Verhulst and J.P.Fryns, Behavioral
and emotional problems in youngsters with PRADER-WILLI
syndrome. Genetic Counselling 2 (1991) 33-41.
Descheemaeker, M.J., A.Swillen, L.Plissart, M.
Borghgraef, S.Rasenberg, L.M.G.Curfs and J.P.Fryns,
The PRADER-WILLI syndrome: A self supporting program
for children, youngsters and adults. Genet.Counseling
5 (1994) 199-205.
Kennerknecht,I., Differentiated recurrence risk
-estimated in the PRADER-WILLI syndrome. Clin.Genet.
41 (1992) 303-308.
Lee, S.-T., R.D.Nicholls, S.Bundey et al., Mutations
of the P: gene. in oculocutaneous albianism, ocular
albinism and Prader-Willi-Syndrome plus albinism.New
Engl.J-Med. 330 (1994) 529-534.
Pagnan,N.A.B., and T.R.Gollop, PRADER-WILLI habitus,
osteopenia and camptodactyly (Urban-Rogers-MEYER
syndrome): A probable second report. Am.J.Med.Genet.
31 (1988) 787-792.
Rivera,H., 0.Zuffardi and L.Gargantini, Nonreciprocal
and jumping translocations of 15q1-qter in PRADER-WILLI
syndrome.
Am.J.Med.Genet. 37 (1990) 311-317.
Literaturverzeichnis aus PWS Buch
1 . Angelman H (1965). "Puppet" children:
A report on three cases. Dev Med Child Neurol 7:681
683, 1965.
2. Aughton DJ and Cassidy SB (1990). Physical features
of PraderWilli syndrome in neonates. Am J Dis Child
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3. Greenswag LR (1987). Adults with Prader-Willi
syndrome: A survey of 232 cases. Dev Med Child Neurol
29:145-152.
4. Holm VA (1981). The diagnosis ot Prader-Willi-syndrome.
In Holm VA, Sulzbacher S, and Pipes PL (eds), Prader-Willi
Syndrome. Baitimore, University Park Press, ch.
3.
5. Knoll J, Nicholls R, Magenis R, Graham J Jr (1989).
Angelman and Prader-Wilii syndrome share a common
chromosome 15 deletion but differ in parental origin
of the deletion. Am J Med Genet 32:285-290.
6. Ledbetter, D. H., Riccardi VM, Airhart SD, Strobel
RJ, Keenen SB, and Crawford JD (1981 ). Deletions
of chromosome 15 as a cause of the Prader-Willi
syndrome. N. Engl J Med 304:325329.
7. Lee PDK, W_lson DM, Ronntree L, Hintz RL, Rosenfeld
RG (1987). Linear growth response to exogeneous
growth hormone in Prader-Willi syndrome. Am J Med
Genet 28:865-871.
8. Nicholis RD, Knoll JHM< Butler MG, Karam S,
Lalande M (1989). Genetic imprinting suggested by
maternal heterodisomy in nondeletion Prader-Wilii
syndrome. Nature 342:281-285.
9. Prader A, Labhart A, and Willi H (1956). Ein
Syndrom von Adipositas, Kleinwuchs, Kryptorchismus
und Oligophrenie nach Myotonicartigem Zustand in
Neugeborenenalter. Schweiz Med Wochenschr 86: 1260-
1261 .
10. Whitman, BY and Accardo P (1987). Emotional
symptoms in Prader-Willi syndrome adoleseents. Am
J Med Genet 28:897- 905.
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