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7. A hypotonic infant. SLY M; HORNER FA; BOYARSKY LL; PACKER JT Clin Pediatr (Phila); 1963 Mar; 2():127-31. PubMed ID: 13989294 [No Abstract] [Full Text] [Related]
8. The child with congenital anomalies and interstitial deletion of the long arm of chromosome 4. Lech H; Kubalska J; Wisńiewski L Klin Padiatr; 1982 Mar; 194(2):117-9. PubMed ID: 7098371 [No Abstract] [Full Text] [Related]
10. [Atonic-astatic type of encephalopathy in child or Oppenheim's disease?]. VOJIR R Neurol Psychiatr Ceskoslov; 1951 Aug; 14(2-4):82-5. PubMed ID: 14910801 [No Abstract] [Full Text] [Related]
11. [Some hypotonias of the newborn]. THOMAS A; SAINT-ANNE-DARGASSIES Etudes Neonatales; 1952 Dec; 1(4):115-28. PubMed ID: 13043586 [No Abstract] [Full Text] [Related]
12. What syndrome is this? Killian-Teschler-Nicola syndrome. Ohman AB; Pride HB; Papa CA Pediatr Dermatol; 2000; 17(2):151-3. PubMed ID: 10792810 [No Abstract] [Full Text] [Related]
13. Differential diagnosis of infantile hypotonia. The use of the electromyograph and the developmental and neurologic examination as aids. JEBSEN RH; JOHNSON EW; KNOBLOCH H; GRANT DK Am J Dis Child; 1961 Jan; 101():8-17. PubMed ID: 13789718 [No Abstract] [Full Text] [Related]
16. Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37). Gorski JL; Cox BA; Kyine M; Uhlmann W; Glover TW Am J Med Genet; 1989 Mar; 32(3):350-2. PubMed ID: 2729355 [TBL] [Abstract][Full Text] [Related]
17. [Infant hypotonia, obesity, hypogenitalism and oligophrenia--new viewpoints on the etiology and symptoms of Prader-Willi syndrome]. Witkowski R; Ullrich E; Pietsch P; Weber K; Heller K; Losanowa T; Nitz I Psychiatr Neurol Med Psychol (Leipz); 1985 May; 37(5):255-61. PubMed ID: 4023109 [TBL] [Abstract][Full Text] [Related]
18. The floppy infant: recent advances in the understanding of disorders affecting the neuromuscular junction. Gay CT; Bodensteiner JB Neurol Clin; 1990 Aug; 8(3):715-25. PubMed ID: 2215465 [TBL] [Abstract][Full Text] [Related]
19. Supernumerary small chromosomal anomaly: report of three cases including one with a familial inversion of chromosome 5. Lee Ml; Schneider J; Wasant P; Yu CY; Trpis L; Liang YW; Lewis BM; Borkowf S; Borgaonkar DS J Genet Hum; 1978 Sep; 26(3):275-85. PubMed ID: 739263 [TBL] [Abstract][Full Text] [Related]
20. [Association of neuromotor retardation and chromosome lqH report of a case]. Jorge SM; Ribeiro VM; Ferrari I; Moreira LM Arq Neuropsiquiatr; 1976 Dec; 34(4):377-8. PubMed ID: 985150 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]