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24. [The oro-facial-digital syndrome. Symptoms and prognosis]. Majewski F; Lenz W; Pfeiffer RA; Tünte W; Müller H Z Kinderheilkd; 1972; 112(1):89-112. PubMed ID: 4336265 [No Abstract] [Full Text] [Related]
25. Syndrome of microcephaly, deafness/malformed ears, mental retardation and peculiar facies in a mother and son. Kawashima H; Tsuji N Clin Genet; 1987 May; 31(5):303-7. PubMed ID: 3608216 [TBL] [Abstract][Full Text] [Related]
26. An extremely rare case of Oro-facial digital syndrome: A case report. Dwivedi S; Thakur A Spec Care Dentist; 2024; 44(2):421-427. PubMed ID: 37095590 [TBL] [Abstract][Full Text] [Related]
27. Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23. Mowat DR; Croaker GD; Cass DT; Kerr BA; Chaitow J; Adès LC; Chia NL; Wilson MJ J Med Genet; 1998 Aug; 35(8):617-23. PubMed ID: 9719364 [TBL] [Abstract][Full Text] [Related]
28. Syndrome of polydactyly, cleft lip, lingual hamartomas, renal hypoplasia, hearing loss, and psychomotor retardation: variant of the Mohr syndrome or a new syndrome? Mattei JF; Aymé S J Med Genet; 1983 Dec; 20(6):433-5. PubMed ID: 6686259 [TBL] [Abstract][Full Text] [Related]
29. Mandibulofacial dysostosis, microcephaly and thorax deformities in two brothers: a new recessive syndrome? Delb W; Lipfert S; Henn W Clin Dysmorphol; 2001 Apr; 10(2):105-9. PubMed ID: 11310989 [TBL] [Abstract][Full Text] [Related]
30. [Oral-facial-digital syndrome in male (author's transl)]. Gracia R; Prieto G; Pérez Rodríguez J; Lledó G; Herráiz JI; Jover P An Esp Pediatr; 1976; 9(1):79-84. PubMed ID: 1267303 [TBL] [Abstract][Full Text] [Related]
31. Microcephaly, micrognathia, and bird-headed dwarfism: prenatal diagnosis of a Seckel-like syndrome. Majoor-Krakauer DF; Wladimiroff JW; Stewart PA; van de Harten JJ; Niermeijer MF Am J Med Genet; 1987 May; 27(1):183-8. PubMed ID: 3300331 [TBL] [Abstract][Full Text] [Related]
32. Prenatal monitoring and genetic counseling in a 47, XXX female with the oro-facial digital syndrome-type 1. Cohen MM; Charrow J; Nadler HL Am J Hum Genet; 1981 Jul; 33(4):649-50. PubMed ID: 7258190 [No Abstract] [Full Text] [Related]
33. The syndrome of retinal pigmentary degeneration, microcephaly, and severe mental retardation (Mirhosseini-Holmes-Walton syndrome): report of two patients. Mendez HM; Paskulin GA; Vallandro C Am J Med Genet; 1985 Oct; 22(2):223-8. PubMed ID: 4050854 [TBL] [Abstract][Full Text] [Related]
34. Oral-facial-digital syndrome with retinal abnormalities: OFDS type IX. A further case report. Nevin NC; Silvestri J; Kernohan DC; Hutchinson WM Am J Med Genet; 1994 Jul; 51(3):228-31. PubMed ID: 8074150 [TBL] [Abstract][Full Text] [Related]
35. A syndrome of microcephaly, mental retardation, unusual facies, cleft palate, and weight deficiency. Weaver DD; Williams CP Birth Defects Orig Artic Ser; 1977; 13(3B):69-84. PubMed ID: 890101 [TBL] [Abstract][Full Text] [Related]
38. CRIPT exonic deletion and a novel missense mutation in a female with short stature, dysmorphic features, microcephaly, and pigmentary abnormalities. Leduc MS; Niu Z; Bi W; Zhu W; Miloslavskaya I; Chiang T; Streff H; Seavitt JR; Murray SA; Eng C; Chan A; Yang Y; Lalani SR Am J Med Genet A; 2016 Aug; 170(8):2206-11. PubMed ID: 27250922 [TBL] [Abstract][Full Text] [Related]
39. The heterogeneity of oral-facial-digital anomalies. Report of a case of Mohr syndrome. Bonioli E; Ruffa G; Baldini A; Giovannini L; Gemme G Panminerva Med; 1979; 21(3):127-30. PubMed ID: 554046 [No Abstract] [Full Text] [Related]
40. [Orofaciodigital syndrome type I in a mother and daughter]. Guerrero Vázquez J; Cazenave Bernal A; de Paz Aparicio P; Luengo Casasola JL; Garcés Ramos A; López Vázquez JL; Hoyos Madrid JJ An Esp Pediatr; 1988 Jan; 28(1):59-62. PubMed ID: 3279888 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]