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Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
86 related items for PubMed ID: 7093017
1. [Holt syndrome: an autosomal dominant, heterogeneous, acral malformation]. Hernández Téllez A, Corona Rivera E, Martínez-Basalo C, Nazará Cazorla Z, Aguirre-Negrete MG, Cantú JM. Bol Med Hosp Infant Mex; 1982 Feb; 39(2):131-3. PubMed ID: 7093017 [No Abstract] [Full Text] [Related]
2. [Stapes ankylosis as a symptom of autosomal dominant symphalangia]. Theunissen EJ, Cremers CW. Ned Tijdschr Geneeskd; 1984 Apr 14; 128(15):712-4. PubMed ID: 6717641 [No Abstract] [Full Text] [Related]
3. Craniosynostosis, Philadelphia type: a new autosomal dominant syndrome with sagittal craniosynostosis and syndactyly of the fingers and toes. Robin NH, Segel B, Carpenter G, Muenke M. Am J Med Genet; 1996 Mar 15; 62(2):184-91. PubMed ID: 8882401 [Abstract] [Full Text] [Related]
4. Holt-Oram syndrome: postaxial and central polydactyly as variable manifestations in a four generations family. Moens P, De Smet L, Fabry G, Fryns JP. Genet Couns; 1993 Mar 15; 4(4):277-80. PubMed ID: 8110414 [No Abstract] [Full Text] [Related]
12. Relatively high prevalence of the Meckel syndrome among Jews. Fried K. Isr J Med Sci; 1973 Jan 15; 9(9):1399. PubMed ID: 4775123 [No Abstract] [Full Text] [Related]
19. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome. Bonioli E, Palmieri A, Bertola A, Bellini C. Genet Couns; 1995 Jan 15; 6(4):309-12. PubMed ID: 8775417 [Abstract] [Full Text] [Related]