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3. Raine syndrome: report of a family with three affected sibs and further delineation of the syndrome. Hülskamp G; Wieczorek D; Rieder H; Louwen F; Hörnig-Franz I; Rickert CH; Horst J; Harms E; Rehder H Clin Dysmorphol; 2003 Jul; 12(3):153-60. PubMed ID: 14564151 [TBL] [Abstract][Full Text] [Related]
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5. New distinct lethal osteosclerotic bone dysplasia (Raine syndrome). Kan AE; Kozlowski K Am J Med Genet; 1992 Jul; 43(5):860-4. PubMed ID: 1642277 [TBL] [Abstract][Full Text] [Related]
6. Raine syndrome: report of a case with hand and foot anomalies. Mahafza T; El-Shanti H; Omari H Clin Dysmorphol; 2001 Jul; 10(3):227-9. PubMed ID: 11446420 [No Abstract] [Full Text] [Related]
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9. Further delineation of Raine syndrome. Al-Gazali LI; Jehier K; Nazih B; Abtin F; Haas D; Sadagahatian R Clin Dysmorphol; 2003 Apr; 12(2):89-93. PubMed ID: 12868469 [TBL] [Abstract][Full Text] [Related]
10. Osteopathia striata with cranial sclerosis: variable expressivity in a four generation pedigree. König R; Dukiet C; Dörries A; Zabel B; Fuchs S Am J Med Genet; 1996 May; 63(1):68-73. PubMed ID: 8723089 [TBL] [Abstract][Full Text] [Related]
15. Hereditary deletion of the entire FAM20C gene in a patient with Raine syndrome. Ababneh FK; AlSwaid A; Youssef T; Al Azzawi M; Crosby A; AlBalwi MA Am J Med Genet A; 2013 Dec; 161A(12):3155-60. PubMed ID: 24039075 [TBL] [Abstract][Full Text] [Related]
16. A case of Raine syndrome presenting with facial dysmorphy and review of literature. Sheth J; Bhavsar R; Gandhi A; Sheth F; Pancholi D BMC Med Genet; 2018 May; 19(1):76. PubMed ID: 29751744 [TBL] [Abstract][Full Text] [Related]
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18. Fetal ultrasonographic findings including cerebral hyperechogenicity in a patient with non-lethal form of Raine syndrome. Tamai K; Tada K; Takeuchi A; Nakamura M; Marunaka H; Washio Y; Tanaka H; Miya F; Okamoto N; Kageyama M Am J Med Genet A; 2018 Mar; 176(3):682-686. PubMed ID: 29341424 [TBL] [Abstract][Full Text] [Related]
19. Osteosclerosis, hypoplastic nose, and proptosis (Raine syndrome): further delineation. Shalev SA; Shalev E; Reich D; Borochowitz ZU Am J Med Genet; 1999 Sep; 86(3):274-7. PubMed ID: 10482879 [TBL] [Abstract][Full Text] [Related]
20. Central nervous system malformations, dense bones and facial dysmorphism: a new autosomal recessive syndrome. al-Gazali LI; Bakalinova D; Bakir M Clin Dysmorphol; 1998 Apr; 7(2):123-6. PubMed ID: 9571283 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]