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25. Costello syndrome: a postnatal growth retardation syndrome with distinct phenotype. Fryns JP; Vogels A; Haegeman J; Eggermont E; van den Berghe H Genet Couns; 1994; 5(4):337-43. PubMed ID: 7888135 [TBL] [Abstract][Full Text] [Related]
26. The phenotypic and cytogenetic spectrum of partial trisomy 9. Wilson GN; Raj A; Baker D Am J Med Genet; 1985 Feb; 20(2):277-82. PubMed ID: 3976721 [TBL] [Abstract][Full Text] [Related]
27. Schinzel-Giedion syndrome. A patient with hypothyroidism and diabetes insipidus. Santos H; Cordeiro I; Medeira A; Mendonça E; Antunes NL; Rosa FC Genet Couns; 1994; 5(2):187-9. PubMed ID: 7917131 [TBL] [Abstract][Full Text] [Related]
28. [Cohen syndrome: report of two cases in female twins]. Arcas Martínez J; García Peñas JJ; Ramos Lizana J; Díaz González C; Pascual Castroviejo I An Esp Pediatr; 1991 Jan; 34(1):83-5. PubMed ID: 2018266 [No Abstract] [Full Text] [Related]
29. Cardio-facio-cutaneous (CFC) syndrome: report of a new patient. Chrzanowska K; Fryns JP; Van den Berghe H Am J Med Genet; 1989 Aug; 33(4):471-3. PubMed ID: 2596505 [TBL] [Abstract][Full Text] [Related]
30. [Acceleration of bone maturation and dysmorphic syndrome in 2 siblings (Marshall-Weaver syndrome)]. Jalaguier J; Montoya F; Germain M; Bonnet H J Genet Hum; 1983 Dec; 31 Suppl 5():385-95. PubMed ID: 6674414 [TBL] [Abstract][Full Text] [Related]
32. Acrocallosal syndrome in two African brothers born to consanguineous parents. Christianson AL; Venter PA; Du Toit JL; Shipalana N; Gericke GS Am J Med Genet; 1994 Jun; 51(2):98-101. PubMed ID: 8092201 [TBL] [Abstract][Full Text] [Related]
33. Kabuki make-up (Niikawa-Kuroki) syndrome in a girl presenting with vitiligo vulgaris, cleft palate, somatic and psychomotor retardation and facial dysmorphism. Schrander-Stumpel C; Theunissen P; Hulsmans R; Fryns JP Genet Couns; 1993; 4(1):71-2. PubMed ID: 8471227 [No Abstract] [Full Text] [Related]
34. The Neu-COFS (cerebro-oculo-facio-skeletal) syndrome: report of a case. Silengo MC; Davi G; Bianco R; Biagioli M; Franceschini P; Cavallo M; Bussi G Clin Genet; 1984 Feb; 25(2):201-4. PubMed ID: 6705255 [TBL] [Abstract][Full Text] [Related]
35. Schinzel acrocallosal syndrome: a variant example of the Greig syndrome? Legius E; Fryns JP; Casaer P; Boel M; Eggermont E Ann Genet; 1985; 28(4):239-40. PubMed ID: 3879437 [TBL] [Abstract][Full Text] [Related]
36. Constitutional interstitial deletion of 17(p11.2) (Smith-Magenis syndrome): a clinically recognizable microdeletion syndrome. Report of two cases and review of the literature. Fischer H; Oswald HP; Duba HC; Doczy L; Simma B; Utermann G; Haas OA Klin Padiatr; 1993; 205(3):162-6. PubMed ID: 8350589 [TBL] [Abstract][Full Text] [Related]
37. An infant with Beckwith-Wiedemann syndrome and chromosomal duplication 11p13----pter.: correlation of symptoms between 11p trisomy and Beckwith-Wiedemann syndrome. Okano Y; Osasa Y; Yamamoto H; Hase Y; Tsuruhara T; Fujita H Jinrui Idengaku Zasshi; 1986 Dec; 31(4):365-72. PubMed ID: 3613243 [No Abstract] [Full Text] [Related]
38. Costello syndrome: the natural history of a true postnatal growth retardation syndrome. Umans S; Decock P; Fryns JP Genet Couns; 1995; 6(2):121-5. PubMed ID: 7546454 [TBL] [Abstract][Full Text] [Related]
39. Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome? Bindewald B; Ulmer H; Müller U Am J Med Genet; 1994 Apr; 50(2):173-6. PubMed ID: 8010348 [TBL] [Abstract][Full Text] [Related]
40. Fryns syndrome: another example of non-lethal outcome with severe mental handicap. Hanssen AM; Schrander-Stumpel CT; Thiry PA; Fryns JP Genet Couns; 1992; 3(4):187-93. PubMed ID: 1472353 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]