Published in Clin Genet on January 01, 1992
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Vasopressin and gonadotropin deficiency in a boy with the ectrodactyly-ectodermal dysplasia-clefting syndrome. Acta Paediatr (1992) 0.92
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A novel form of syndromic cutis laxa with facial dysmorphism, cleft palate, and mental retardation. J Med Genet (2004) 0.84
Pure terminal duplication of the short arm of chromosome 19 in a boy with mild microcephaly. J Med Genet (2002) 0.84
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[A case of Kabuki syndrome admitted for acute diarrhea and growth retardation in a French hospital in tropical area]. Arch Pediatr (2010) 0.82
Private multiple congenital anomaly syndromes may result from unbalanced subtle translocations: t(2q;4p) explains the Lambotte syndrome. Am J Med Genet (1997) 0.82
Orofacial clefting: update on the role of genetics. B-ENT (2006) 0.81
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