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.
123 related articles for article (PubMed ID: 8055131)
61. Blepharophimosis, minor facial anomalies, genital anomalies, and mental retardation: report of two sibs with a unique syndrome. Nowaczyk MJ; Sutcliffe TL Am J Med Genet; 1999 Nov; 87(1):78-81. PubMed ID: 10528253 [TBL] [Abstract][Full Text] [Related]
62. [Mobius syndrome: report of a case]. Nishida F; Nishino M Shoni Shikagaku Zasshi; 1987; 25(1):193-8. PubMed ID: 3506296 [No Abstract] [Full Text] [Related]
63. [Sporadic appearance of the Marinesco-Sjögren syndrome]. Kofer J; Bejsovec M Cesk Neurol Neurochir; 1982 Mar; 45(2):113-6. PubMed ID: 7094097 [No Abstract] [Full Text] [Related]
64. A distinctive syndrome of brachycephaly, deafness, cataracts and mental retardation. Suthers GK; Earley AE; Huson SM Clin Dysmorphol; 1993 Oct; 2(4):342-5. PubMed ID: 7508318 [TBL] [Abstract][Full Text] [Related]
65. A Japanese boy with Young-Simpson syndrome. Nakamura T; Noma S Acta Paediatr Jpn; 1997 Aug; 39(4):472-4. PubMed ID: 9316295 [TBL] [Abstract][Full Text] [Related]
66. [A rare case of accumulation of dental anomalies. Dental anomalies from a case load of a district dentist 12]. Sárhegyi J Fogorv Sz; 1992 Jan; 85(1):17-20. PubMed ID: 1551447 [No Abstract] [Full Text] [Related]
68. Kaufman oculocerebrofacial syndrome: report of two new cases and further delineation. Figuera LE; García-Cruz D; Ramírez-Dueñas ML; Rivera-Robles V; Cantù JM Clin Genet; 1993 Aug; 44(2):98-101. PubMed ID: 8275567 [TBL] [Abstract][Full Text] [Related]
69. A newly recognized syndrome with double upper and lower lip, hypertelorism, eyelid ptosis, blepharophimosis, and third finger clinodactyly. Parmar RC; Muranjan MN Am J Med Genet A; 2004 Jan; 124A(2):200-1. PubMed ID: 14699621 [TBL] [Abstract][Full Text] [Related]
70. [Marden-Walker syndrome. New case and discussion about its role in arthrogryposes]. Manouvrier-Hanu S; de la Chapelle AC; Farriaux JP Pediatrie; 1988; 43(4):313-7. PubMed ID: 3047662 [TBL] [Abstract][Full Text] [Related]
71. Skeletal manifestations in Ohdo syndrome: a case with bilateral patella dislocations. Day R; Fryer A Clin Dysmorphol; 2004 Jan; 13(1):17-9. PubMed ID: 15127758 [TBL] [Abstract][Full Text] [Related]
72. A female patient with X-linked Ohdo syndrome of the Maat-Kievit-Brunner phenotype caused by a novel variant of MED12. Murakami H; Enomoto Y; Tsurusaki Y; Sugio Y; Kurosawa K Congenit Anom (Kyoto); 2020 May; 60(3):91-93. PubMed ID: 31322785 [No Abstract] [Full Text] [Related]
73. A 24-year-Old Male with Marden-Walker Syndrome and Epilepsy: Case Report. Rissardo JP; Fornari Caprara AL; Fighera MR; Tamiozzo RL Neurol India; 2023; 71(4):767-771. PubMed ID: 37635513 [TBL] [Abstract][Full Text] [Related]
74. Blepharophimosis, blepharoptosis, defects of the anterior chamber of the eye, caudal appendage, radioulnar synostosis, hearing loss and umbilical anomalies in sibs: 3MC syndrome? Leal GF; Silva EO; Duarte AR; Campos JF Am J Med Genet A; 2008 Apr; 146A(8):1059-62. PubMed ID: 18266249 [No Abstract] [Full Text] [Related]
75. Deafness associated with bilateral facial diplegia, ptosis and hypermobile joints--A new autosomal recessive condition? Reardon W; McGinn M; King MD; Earley M Am J Med Genet A; 2003 Sep; 122A(1):84-8. PubMed ID: 12949979 [TBL] [Abstract][Full Text] [Related]
76. Lipomatous myelomeningocele, athyrotic hypothyroidism, and sensorineural deafness: a new form of syndromal deafness? Peters HL; Bankier A J Med Genet; 1998 Nov; 35(11):948-50. PubMed ID: 9832044 [TBL] [Abstract][Full Text] [Related]
78. [Goltz's syndrome in a boy]. Walbaum R; Samaille G; Dehaene P Pediatrie; 1970 Dec; 25(8):911-20. PubMed ID: 5494357 [No Abstract] [Full Text] [Related]
79. Fine-Lubinsky syndrome: a fourth patient with brachycephaly, deafness, cataract, microstomia and mental retardation. Aymé S; Philip N Clin Dysmorphol; 1996 Jan; 5(1):55-60. PubMed ID: 8867660 [TBL] [Abstract][Full Text] [Related]
80. [COMPLICATED FAMILIAL BLEPHAROPHIMOSIS. STUDY OF MEMBERS OF THE BLE FAMILY]. SACREZ R; FRANCFORT J; JUIF JG; DE GROUCHY J Ann Pediatr (Paris); 1963 Oct; 10():493-501. PubMed ID: 14095147 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]