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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

280 related articles for article (PubMed ID: 1632438)

  • 61. Richieri-Costa-Pereira syndrome: Expanding its phenotypic and genotypic spectrum.
    Bertola DR; Hsia G; Alvizi L; Gardham A; Wakeling EL; Yamamoto GL; Honjo RS; Oliveira LAN; Di Francesco RC; Perez BA; Kim CA; Passos-Bueno MR
    Clin Genet; 2018 Apr; 93(4):800-811. PubMed ID: 29112243
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Autosomal recessive blepharoptosis, cleft lip/palate, dental anomalies, and ectrodactyly.
    Rodini ES; Richieri-Costa A
    Am J Med Genet; 1992 Feb; 42(3):340-2. PubMed ID: 1536175
    [No Abstract]   [Full Text] [Related]  

  • 63. Catel-Manzke syndrome: a clinical report suggesting autosomal recessive inheritance.
    Kiper PÖ; Utine GE; Boduroğlu K; Alanay Y
    Am J Med Genet A; 2011 Sep; 155A(9):2288-92. PubMed ID: 21834032
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Genetics of acheiropodia ("the handless and footless families of Brazil"): XI. Pathologic aspects.
    Marçallo FA; Pilotto RF; Freire-Maia A
    Am J Med Genet; 1979; 4(3):287-91. PubMed ID: 517582
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Short stature, microcephaly, characteristic face, syndactyly and mental retardation: the Filippi syndrome. Report on a second family.
    Meinecke P
    Genet Couns; 1993; 4(2):147-51. PubMed ID: 8395190
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Postaxial acrofacial dysostosis: report of a Brazilian patient.
    Richieri-Costa A; Guion-Almeida ML
    Am J Med Genet; 1989 Aug; 33(4):447-9. PubMed ID: 2596501
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Autosomal recessive Silver-Russell syndrome.
    Teebi AS
    Clin Dysmorphol; 1992 Jul; 1(3):151-6. PubMed ID: 1285272
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Cortical blindness, growth and psychomotor retardation and postaxial polydactyly: a probably distinct autosomal recessive syndrome.
    Hernández A; García-Esquivel L; Reynoso MC; Fragoso R; Enríquez-Guerra MA; Nazará Z; Anzar MB; Cantú JM
    Clin Genet; 1985 Sep; 28(3):251-4. PubMed ID: 4064363
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Combined immunodeficiency, facial dysmorphism, optic nerve atrophy, skeletal anomalies and developmental delay: a new syndrome.
    Roifman CM; Chitayat D
    Clin Genet; 2009 Nov; 76(5):449-57. PubMed ID: 19863561
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Acheiropody. A report of two cases.
    Kruger LM; Kumar A
    J Bone Joint Surg Am; 1994 Oct; 76(10):1557-60. PubMed ID: 7929505
    [No Abstract]   [Full Text] [Related]  

  • 71. Diastasis of the tibiofibular mortise, hypoplasia of the tibia, and clubfoot, in a neonate with cleft hand and cardiac anomalies. A case report.
    Matthews WE; Mubarak SJ; Carroll NC
    Clin Orthop Relat Res; 1977; (126):216-9. PubMed ID: 598121
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Choanal atresia, syngnathia, brachydactyly, mental retardation and short stature: an X-linked syndrome?
    Jongmans MCJ; Pfundt R; Hehir-Kwa JY; Brunner HG; Kerstjens-Frederikse WS
    Clin Dysmorphol; 2010 Jan; 19(1):30-32. PubMed ID: 19730370
    [No Abstract]   [Full Text] [Related]  

  • 73. Freeman-Sheldon syndrome. A case report and review of the literature.
    Ferrari D; Bettuzzi C; Donzelli O
    Chir Organi Mov; 2008 Sep; 92(2):127-31. PubMed ID: 18677448
    [TBL] [Abstract][Full Text] [Related]  

  • 74. A new multiple congenital anomaly, mental retardation syndrome with preaxial brachydactyly, hyperphalangism, deafness and orodental anomalies.
    Temtamy SA; Meguid NA; Ismail SI; Ramzy MI
    Clin Dysmorphol; 1998 Oct; 7(4):249-55. PubMed ID: 9823490
    [TBL] [Abstract][Full Text] [Related]  

  • 75. New lethal acrofacial dysostosis syndrome.
    Hecht JT
    Am J Med Genet; 1992 Feb; 42(3):400-1. PubMed ID: 1536191
    [No Abstract]   [Full Text] [Related]  

  • 76. Acrofacial dysostosis syndrome type Rodriguez: a new lethal MCA syndrome.
    Petit P; Moerman P; Fryns JP
    Am J Med Genet; 1992 Feb; 42(3):343-5. PubMed ID: 1536176
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Mental retardation, Robin sequence, and brachydactyly: further confirmation of a new syndrome.
    Gurrieri F; Scarano G; Garavelli L; Della Monica M; Lonardo F; Cuda D; Banchini G; Opitz JM; Neri G
    Am J Med Genet A; 2004 Apr; 126A(2):204-7. PubMed ID: 15057987
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Popliteal pterygium syndrome. Evidence for a severe autosomal recessive form.
    Bartsocas CS; Papas CV
    J Med Genet; 1972 Jun; 9(2):222-6. PubMed ID: 4339984
    [No Abstract]   [Full Text] [Related]  

  • 79. Craniofacial anomalies, ocular findings, pigmented nevi, camptodactyly, and skeletal changes: a possible new autosomal recessive disorder.
    Gül D; Oktenli C; Sağlam M; Erdem U
    Clin Dysmorphol; 2000 Jan; 9(1):61-2. PubMed ID: 10649801
    [TBL] [Abstract][Full Text] [Related]  

  • 80. A noncoding expansion in EIF4A3 causes Richieri-Costa-Pereira syndrome, a craniofacial disorder associated with limb defects.
    Favaro FP; Alvizi L; Zechi-Ceide RM; Bertola D; Felix TM; de Souza J; Raskin S; Twigg SR; Weiner AM; Armas P; Margarit E; Calcaterra NB; Andersen GR; McGowan SJ; Wilkie AO; Richieri-Costa A; de Almeida ML; Passos-Bueno MR
    Am J Hum Genet; 2014 Jan; 94(1):120-8. PubMed ID: 24360810
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.