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Journal Abstract Search
142 related items for PubMed ID: 1030364
21. [49,XXXXY syndrome in a 5-year-old boy]. Wiśniewski L, Krajewska-Walasek M, Lech H, Mospinek M. Pediatr Pol; 1980 Jan; 55(1):81-6. PubMed ID: 7189276 [No Abstract] [Full Text] [Related]
28. Autosomal recessive Robinow syndrome. Teebi AS. Am J Med Genet; 1990 Jan 24; 35(1):64-8. PubMed ID: 2301471 [Abstract] [Full Text] [Related]
29. A whistling face syndrome case with bilateral skin dimples. Buyukavci M, Tan H, Eren S, Balci S. Genet Couns; 2005 Jan 24; 16(1):71-3. PubMed ID: 15844782 [Abstract] [Full Text] [Related]
35. Median cleft face syndrome associated with orbital hypertelorism and polysyndactyly. Ide CH, Holt JE. Eye Ear Nose Throat Mon; 1975 Apr 24; 54(4):150-1. PubMed ID: 164373 [No Abstract] [Full Text] [Related]
36. Median cleft face syndrome. Edwards WC, Askew W, Weisskopf B. Am J Ophthalmol; 1971 Jul 30; 72(1):202-5. PubMed ID: 5571207 [No Abstract] [Full Text] [Related]
38. The hypertelorism microtia clefting syndrome. Baraitser M. J Med Genet; 1982 Oct 30; 19(5):387-8. PubMed ID: 7143395 [Abstract] [Full Text] [Related]
39. [Aarskog's syndrome (facial-digital-genital syndrome). Study of a family (author's transl)]. Scarano G, Rinaldi MM, Cavaliere ML, Esposito M, Sicolo A, Santulli B, Stabile M, Fasano R, Ventruto V. Pediatr Med Chir; 1981 Oct 30; 3(4):323-5. PubMed ID: 7343926 [Abstract] [Full Text] [Related]
40. [Partial trisomy of chromosome 22 in an infant]. Rogóyski A, Babel M, Tronowska TD. Pediatr Pol; 1983 Jun 30; 58(6):561-4. PubMed ID: 6646916 [No Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]