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.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
383 related items for PubMed ID: 7717420
21. Peters'-Plus syndrome with agenesis of the corpus callosum: report of a case and confirmation of autosomal recessive inheritance. Camera G, Centa A, Pozzolo S, Camera A. Clin Dysmorphol; 1993 Oct; 2(4):317-21. PubMed ID: 8305962 [Abstract] [Full Text] [Related]
27. Acrocallosal syndrome in a child with de novo inverted tandem duplication of 12p11.2-p13.3. Pfeiffer RA, Legat G, Trautmann U. Ann Genet; 1992 Oct; 35(1):41-6. PubMed ID: 1610119 [Abstract] [Full Text] [Related]
32. [Townes-Brocks syndrome. Case report and review of the literature]. Kotzot D, Lorenz P, Bieber A, Gröbe H. Monatsschr Kinderheilkd; 1992 Jun; 140(6):343-5. PubMed ID: 1640945 [Abstract] [Full Text] [Related]
36. Callosal defect, microcephaly, severe mental retardation, and other anomalies in three sibs. da-Silva EO. Am J Med Genet; 1988 Apr; 29(4):837-43. PubMed ID: 3400727 [Abstract] [Full Text] [Related]
37. Floating-Harbor syndrome in a Kuwaiti patient: a case report and literature review. Bastaki L, El-Nabi MM, Azab AS, Gouda SA, Al-Wadaani AM, Naguib KK. East Mediterr Health J; 2007 Apr; 13(4):975-9. PubMed ID: 17955782 [No Abstract] [Full Text] [Related]
39. Carpenter syndrome with normal intelligence: Brazilian girl born to consanguineous parents. Richieri-Costa A, Pirolo Júnior L, Cohen MM. Am J Med Genet; 1993 Aug 15; 47(2):281-3. PubMed ID: 8213921 [Abstract] [Full Text] [Related]