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3. The Cohen syndrome: does mottled retina separate a Finnish and a Jewish type? Kondo I; Nagataki S; Miyagi N Am J Med Genet; 1990 Sep; 37(1):109-13. PubMed ID: 2240027 [TBL] [Abstract][Full Text] [Related]
4. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome. Bonioli E; Palmieri A; Bertola A; Bellini C Genet Couns; 1995; 6(4):309-12. PubMed ID: 8775417 [TBL] [Abstract][Full Text] [Related]
5. Oliver McFarlane syndrome: a 25-year follow-up. Sampson JR; Tolmie JL; Cant JS Am J Med Genet; 1989 Oct; 34(2):199-201. PubMed ID: 2816997 [TBL] [Abstract][Full Text] [Related]
6. 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]
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10. [Goldman-Favre hyaloid-tapeto-retinal degeneration]. Neetens A; Burvenich H; Hendrata Y; Van Rompaey J; Hofkens R Bull Mem Soc Fr Ophtalmol; 1980; 92():185-90. PubMed ID: 6971684 [No Abstract] [Full Text] [Related]
11. [Microencephalic nanism, severe retardation, hypertonia, obesity, and hypogonadism in two brothers: a new syndrome?]. Delozier-Blanchet CD; Haenggeli CA; Engel E J Genet Hum; 1989 Dec; 37(4-5):353-65. PubMed ID: 2635712 [TBL] [Abstract][Full Text] [Related]
12. Robin sequence with facial and digital anomalies in two half-brothers by the same mother. Chitayat D; Meunier CM; Hodgkinson KA; Azouz ME Am J Med Genet; 1991 Aug; 40(2):167-72. PubMed ID: 1897570 [TBL] [Abstract][Full Text] [Related]
13. Multicore disease in sibs with severe mental retardation, short stature, facial anomalies, hypoplasia of the pituitary fossa, and hypogonadotrophic hypogonadism. Chudley AE; Rozdilsky B; Houston CS; Becker LE; Knoll JH Am J Med Genet; 1985 Jan; 20(1):145-58. PubMed ID: 3970066 [TBL] [Abstract][Full Text] [Related]
14. Acro-oto-ocular syndrome: further evidence for a new autosomal recessive disorder. Bertola DR; Wolf LM; Toriello HV; Netzloff ML Am J Med Genet; 1997 Dec; 73(4):442-6. PubMed ID: 9415472 [TBL] [Abstract][Full Text] [Related]
15. Cleft lip and palate, characteristic facial appearance, malrotation of the intestine, and lethal congenital heart disease in two sibs: a new autosomal recessive condition? McPherson E; Clemens M Am J Med Genet; 1996 Mar; 62(1):58-60. PubMed ID: 8779326 [TBL] [Abstract][Full Text] [Related]