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2. A syndrome of craniofacial, digital, and genital anomalies. Harrod MJ; Keele DK; Howard J Birth Defects Orig Artic Ser; 1977; 13(3B):111-5. PubMed ID: 890088 [No Abstract] [Full Text] [Related]
3. Terminal deletion of the long arm of chromosome 2 in a premature infant with karyotype: 46,XY,del(2)(q37). Wang TH; Johnston K; Hsieh CL; Dennery PA Am J Med Genet; 1994 Feb; 49(4):399-401. PubMed ID: 8160733 [TBL] [Abstract][Full Text] [Related]
4. Ectopia cordis thoracalis with craniofacial defects resulting from early amnion rupture. Van Allen MI; Myhre S Teratology; 1985 Aug; 32(1):19-24. PubMed ID: 4041078 [TBL] [Abstract][Full Text] [Related]
5. Previously undescribed syndrome of craniofacial, hand anomalies, and sensorineural deafness. Sommer A; Young-Wee T; Frye T Am J Med Genet; 1983 May; 15(1):71-7. PubMed ID: 6859126 [TBL] [Abstract][Full Text] [Related]
6. Classification, etiology, and genetic aspects of craniofacial anomalies. Kaye CI Otolaryngol Clin North Am; 1981 Nov; 14(4):827-64. PubMed ID: 7335360 [TBL] [Abstract][Full Text] [Related]
7. A patient with Schinzel-Giedion syndrome and a review of 20 patients. Okamoto N; Takeuchi M; Kitajima H; Hosokawa S Jpn J Hum Genet; 1995 Jun; 40(2):189-93. PubMed ID: 7662999 [TBL] [Abstract][Full Text] [Related]
9. Beare-Stevenson cutis gyrata syndrome. Hall BD; Cadle RG; Golabi M; Morris CA; Cohen MM Am J Med Genet; 1992 Sep; 44(1):82-9. PubMed ID: 1519658 [TBL] [Abstract][Full Text] [Related]
10. An autosomal dominant syndrome of characteristic facial appearance, preauricular pits, fifth finger clinodactyly, and tetralogy of Fallot. Jones MC; Waldman JD Am J Med Genet; 1985 Sep; 22(1):135-41. PubMed ID: 4050848 [TBL] [Abstract][Full Text] [Related]
11. [Trichorhinophalangeal syndrome : analysis of craniofacial architecture in six cases (author's transl)]. Scheffer P; Verdier M; Finidori G Rev Stomatol Chir Maxillofac; 1981; 82(4):230-3. PubMed ID: 6944759 [TBL] [Abstract][Full Text] [Related]
12. Vohwinkel syndrome (mutilating keratoderma) associated with craniofacial anomalies. Sensi A; Bettoli V; Zampino MR; Gandini E; Calzolari E Am J Med Genet; 1994 Apr; 50(2):201-3. PubMed ID: 8010352 [TBL] [Abstract][Full Text] [Related]
13. Syndrome identification case report 90: multiple craniofacial and skeletal defects. Mastroiacovo P; De Rosa G; Satta MA; Colavita N; Priolo F; Pasargiklian E J Clin Dysmorphol; 1983; 1(1):13-5. PubMed ID: 6580383 [No Abstract] [Full Text] [Related]
14. The value of establishing the genetic component in etiology of craniofacial anomalies. Stewart RE Birth Defects Orig Artic Ser; 1980; 16(5):27-33. PubMed ID: 7448376 [No Abstract] [Full Text] [Related]
15. [Two cases of amniotic band disruption complex (author's transl)]. Ronconi GF; Pesenti P; Artusi F; Visonà A; Zanardo V; Giaretta I Pediatr Med Chir; 1981; 3(4):327-30. PubMed ID: 7343927 [TBL] [Abstract][Full Text] [Related]
16. An apparently new acrocraniofacial syndrome with cranial nerve and visceral anomalies. Hameed R; Bissenden JG; Webb WR; Cole TR Clin Dysmorphol; 1999 Jul; 8(3):199-202. PubMed ID: 10457854 [TBL] [Abstract][Full Text] [Related]
17. Persistence of müllerian derivatives, lymphangiectasis, hepatic failure, postaxial polydactyly, renal and craniofacial anomalies. Urioste M; Rodríguez JI; Barcia JM; Martín M; Escribá R; Pardo M; Camino J; Martínez-Frías ML Am J Med Genet; 1993 Sep; 47(4):494-503. PubMed ID: 8256813 [TBL] [Abstract][Full Text] [Related]
20. Six additional cases of the KBG syndrome: clinical reports and outline of the diagnostic criteria. Zollino M; Battaglia A; D'Avanzo MG; Della Bruna MM; Marini R; Scarano G; Cappa M; Neri G Am J Med Genet; 1994 Sep; 52(3):302-7. PubMed ID: 7810561 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]