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Journal Abstract Search
185 related items for PubMed ID: 6212507
21. A family with concurrent mesomelic shortening and hereditary nephritis. Funderburk SJ, Smith L, Falk RE, Bergstein JM, Winter H. Birth Defects Orig Artic Ser; 1976; 12(6):47-61. PubMed ID: 788812 [No Abstract] [Full Text] [Related]
22. Two female siblings from Turkey with Langer mesomelic dysplasia (homozygous Leri-Weill dyschondrosteosis syndrome). Balci S, Zafer Y, Unsal M. Turk J Pediatr; 1999; 41(4):531-9. PubMed ID: 10770125 [Abstract] [Full Text] [Related]
23. [Stenosis of the lumbar spinal canal and dolichophalangy in a case of dyschondrosteosis (author's transl)]. Leone G. Radiol Med; 1979 Dec; 65(12):905-12. PubMed ID: 554217 [Abstract] [Full Text] [Related]
33. Father to son transmission in metaphyseal chondrodysplasia mimicking vitamin D resistant rickets. Held KR, Riebel T, Schaefer E. Prog Clin Biol Res; 1982 Aug; 104():143-8. PubMed ID: 6298812 [No Abstract] [Full Text] [Related]
34. [Mandelung's deformity: manifastation of dyschondrosteosis]. Holenstein P, Buchs P. Z Orthop Ihre Grenzgeb; 1967 Apr; 102(4):585-94. PubMed ID: 4233025 [No Abstract] [Full Text] [Related]
35. Picture of the month. Dyschondrosteosis (Leri-Weil syndrome, Leri's pleonostenosis). Rezvani I, Sharma RK, Collipp PJ. Am J Dis Child; 1971 Nov; 122(5):429-30. PubMed ID: 5129533 [No Abstract] [Full Text] [Related]
40. Isolated mesomelic shortening of the forearm in father and daughter: a new entity in the group of mesomelic dysplasias. Fryns JP, Hofkens G, Fabry G, van den Berghe H. Clin Genet; 1988 Jan 15; 33(1):57-9. PubMed ID: 3342548 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]