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.
43. Spondylometaphyseal dysplasia-Sedaghatian type. Elçioglu N; Hall CM Am J Med Genet; 1998 Apr; 76(5):410-4. PubMed ID: 9556300 [TBL] [Abstract][Full Text] [Related]
44. [Some roentgenological changes in the metaphyseal and epiphyseal zones during disturbances of general body growth in length]. Tikhonov VA Vestn Rentgenol Radiol; 1967; 42(6):52-8. PubMed ID: 5616474 [No Abstract] [Full Text] [Related]
45. Michels syndrome in a Brazilian girl born to consanguineous parents. Guion-Almeida ML; Rodini ES Am J Med Genet; 1995 Jul; 57(3):377-9. PubMed ID: 7677137 [TBL] [Abstract][Full Text] [Related]
46. An unclassifiable type of spondylo-peripheral epiphyseal dysplasia associated with 21 trisomy. Ioan DM; Popa M; Fryns JP Genet Couns; 1993; 4(1):59-62. PubMed ID: 8471223 [TBL] [Abstract][Full Text] [Related]
47. Syndrome of cleft palate, microcephaly, large ears, and short stature (Say syndrome). Abu-Libdeh B; Fujimoto A; Ehinger M Am J Med Genet; 1993 Feb; 45(3):358-60. PubMed ID: 8434624 [TBL] [Abstract][Full Text] [Related]
48. Spondylocarpotarsal synostosis with epiphyseal dysplasia. Honeywell C; Langer L; Allanson J Am J Med Genet; 2002 May; 109(4):318-22. PubMed ID: 11992487 [TBL] [Abstract][Full Text] [Related]
49. New form of spondyloepimetaphyseal dysplasia (SEMD) in Jewish family of Iraqi origin. Shohat M; Lachman R; Carmi R; Bar Ziv J; Rimoin D Am J Med Genet; 1993 Jun; 46(4):358-62. PubMed ID: 8357004 [TBL] [Abstract][Full Text] [Related]
50. Compound heterozygosity for the Achondroplasia-hypochondroplasia FGFR3 mutations: prenatal diagnosis and postnatal outcome. Chitayat D; Fernandez B; Gardner A; Moore L; Glance P; Dunn M; Chun K; Sgro M; Ray P; Allingham-Hawkins D Am J Med Genet; 1999 Jun; 84(5):401-5. PubMed ID: 10360393 [TBL] [Abstract][Full Text] [Related]
51. Polymicrogyria, cerebellar vermis hypoplasia, severe facial dysmorphism and cleft palate: a new syndrome? Mosca AL; Laurent N; Guibaud L; Callier P; Thauvin-Robinet C; Mugneret F; Huet F; Grimaldi M; Gouyon JB; Sandre D; Faivre L Eur J Med Genet; 2007; 50(1):48-53. PubMed ID: 17067864 [TBL] [Abstract][Full Text] [Related]
52. TAR syndrome with orofacial clefting. Midro A; Hubert E; Preferansow J; Iwaszkiewicz-Pawłowska A Genet Couns; 1993; 4(3):187-92. PubMed ID: 8267925 [TBL] [Abstract][Full Text] [Related]
53. The Weissenbacher-Zweymuller syndrome of micrognathia and rhizomelic chondrodysplasia at birth with subsequent normal growth. Haller JO; Berdon WE; Robinow M; Slovis TL; Baker DH; Johnson GF Am J Roentgenol Radium Ther Nucl Med; 1975 Dec; 125(4):936-43. PubMed ID: 813535 [TBL] [Abstract][Full Text] [Related]
54. [Generalized dysplasia of epiphyseal and metaphyseal exostoses in the Rubinstein-Taybi syndrome]. Brandner M; Saur G Fortschr Geb Rontgenstr Nuklearmed; 1972 Sep; 117(3):317-23. PubMed ID: 4342581 [No Abstract] [Full Text] [Related]
55. Sedaghatian congenital lethal metaphyseal chondrodysplasia--observations in a second Iranian family and histopathological studies. Opitz JM; Spranger JW; Stöss HR; Pesch HJ; Azadeh B Am J Med Genet; 1987 Mar; 26(3):583-90. PubMed ID: 3565474 [TBL] [Abstract][Full Text] [Related]
56. A new acro-cranio-facial dysostosis syndrome in sisters. Kaplan P; Plauchu H; Fitch N; Jéquier S Am J Med Genet; 1988 Jan; 29(1):95-106. PubMed ID: 3344780 [TBL] [Abstract][Full Text] [Related]