These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
99 related articles for article (PubMed ID: 6928403)
21. [Prader-Willi syndrome in a young infant]. Hack WW; ten Houten R; Breslau-Suderius EJ; Halley DJ Ned Tijdschr Geneeskd; 1997 Oct; 141(42):2025-8. PubMed ID: 9550755 [TBL] [Abstract][Full Text] [Related]
22. [Development of electrical activity in the central nervous system in central hypotonic syndromes of various cerebral and cerebellar disorders]. Rössler M; Lesný I Cesk Neurol Neurochir; 1981 Jul; 44(4):266-71. PubMed ID: 7273211 [No Abstract] [Full Text] [Related]
23. Pure distal monosomy 10q26 in a patient displaying clinical features of Prader-Willi syndrome during infancy and distinct behavioural phenotype in adolescence. Lukusa T; Fryns JP Genet Couns; 2000; 11(2):119-26. PubMed ID: 10893663 [TBL] [Abstract][Full Text] [Related]
24. [Languaje and hearing in Prader-Willi syndrome]. Sánchez Legaza E; Ciges Juan M; González Pérez M; Miranda Caravallo JI An Otorrinolaringol Ibero Am; 2006; 33(2):175-82. PubMed ID: 16749726 [TBL] [Abstract][Full Text] [Related]
25. [Differential diagnosis of the hypotonic syndrome in infants and children]. Svatý J Cesk Pediatr; 1982 Mar; 37(3):133-7. PubMed ID: 7083374 [No Abstract] [Full Text] [Related]
26. Oral findings in a child with Prader-Labhart-Willi syndrome. Salako NO; Ghafouri HM Quintessence Int; 1995 May; 26(5):339-41. PubMed ID: 7568756 [TBL] [Abstract][Full Text] [Related]
27. Kleine-Levin syndrome in a boy with Prader-Willi syndrome. Gau SF; Soong WT; Liu HM; Hou JW; Tsai WY; Chiu YN; Yeh YC; Wang PJ; Wang TR Sleep; 1996 Jan; 19(1):13-7. PubMed ID: 8650457 [TBL] [Abstract][Full Text] [Related]
28. [Molecular diagnosis of Prader-Willi and Angelman syndromes: methylation, cytogenetics and FISH analysis]. Santa María L; Curotto B; Cortés F; Rojas C; Alliende MA Rev Med Chil; 2001 Apr; 129(4):367-74. PubMed ID: 11413988 [TBL] [Abstract][Full Text] [Related]
29. [Torsion of the large omentum in Prader-Willi syndrome]. Bassetti S; Donati D; Buetti L Schweiz Med Wochenschr; 1995 Jun; 125(22):1089-91. PubMed ID: 7784871 [TBL] [Abstract][Full Text] [Related]
30. Clinical evidence of intrauterine disturbance in Prader-Willi syndrome, a genetically imprinted neurodevelopmental disorder. Dudley O; Muscatelli F Early Hum Dev; 2007 Jul; 83(7):471-8. PubMed ID: 17055193 [TBL] [Abstract][Full Text] [Related]
34. [The hypotonia-hypomentia-hypogonadism-obesity syndrome (Prader-Willi-Labhart syndrome) in a 38-year-old man]. van Bergeijk L; van der Veen EA Ned Tijdschr Geneeskd; 1980 Dec; 124(49):2090-2. PubMed ID: 7442851 [No Abstract] [Full Text] [Related]
36. Language development in a 3-year-old boy with Prader-Willi syndrome. Atkin K; Lorch MP Clin Linguist Phon; 2007 Apr; 21(4):261-76. PubMed ID: 17453868 [TBL] [Abstract][Full Text] [Related]
37. Rectal bleeding in Prader-Willi syndrome. Bhargava SA; Putnam PE; Kocoshis SA; Rowe M; Hanchett JM Pediatrics; 1996 Feb; 97(2):265-7. PubMed ID: 8584392 [TBL] [Abstract][Full Text] [Related]
39. Two Prader-Willi/Angelman syndrome loci present in an isodicentric marker chromosome. Luke S; Verma RS; Giridharan R; Conte RA; Macera MJ Am J Med Genet; 1994 Jul; 51(3):232-3. PubMed ID: 7521122 [TBL] [Abstract][Full Text] [Related]
40. [Central infantile hypotonic syndrome with central nervous system anomalies]. Rössler M; Brachfeld K; Lesný I Cesk Pediatr; 1981 Sep; 36(9):521-3. PubMed ID: 7285220 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]