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Newly recognized syndrome of cerebral, ocular, dental, auricular, skeletal anomalies: CODAS syndrome--a case report.
Am J Med Genet. 1991 Jul 1;40(1):88-93. doi: 10.1002/ajmg.1320400118.
Am J Med Genet. 1991.
PMID: 1887855
Spondylometepiphyseal dysplasia congenita, Strudwick type.
Shebib SM, Chudley AE, Reed MH.
Shebib SM, et al.
Pediatr Radiol. 1991;21(4):298-300. doi: 10.1007/BF02018630.
Pediatr Radiol. 1991.
PMID: 1870932
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Osteodysplastic variant of primordial dwarfism.
Shebib S, Hugosson C, Sakati N, Nyhan WL.
Shebib S, et al.
Am J Med Genet. 1991 Aug 1;40(2):146-50. doi: 10.1002/ajmg.1320400205.
Am J Med Genet. 1991.
PMID: 1897566
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Multiple dysmorphic features and pancytopenia: a new syndrome?
Sackey K, Sakati N, Aur RJ, Shebib S, Sabbah RS, Rifai S.
Sackey K, et al.
Clin Genet. 1985 Jun;27(6):606-10. doi: 10.1111/j.1399-0004.1985.tb02046.x.
Clin Genet. 1985.
PMID: 4017281
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Endodermal sinus (yolk sac) tumor in infants and children. A clinical and pathologic study: an 11 year review.
Shebib S, Sabbah RS, Sackey K, Akhtar M, Aur RJ.
Shebib S, et al.
Am J Pediatr Hematol Oncol. 1989 Spring;11(1):36-9. doi: 10.1097/00043426-198921000-00009.
Am J Pediatr Hematol Oncol. 1989.
PMID: 2712240
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