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A syndrome of intrauterine dwarfism recognizable at birth with craniofacial dysostosis, disproportionate short arms and other anomalies
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Phenotypic and genetic analysis of the Silver-Russell syndrome
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Monozygotic twins discordant for the Russell-Silver syndrome
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Stuck twin syndrome: Outcome in thirty-seven consecutive cases
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The role of velamcntous cord insertion in the etiology of twin-twin transfusion syndrome
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Ring chromosome 15 involving deletion of the insulin-like growth factor 1 receptor gene in a patient with features of Silver-Russell syndrome
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Tamura T, Tohma T, Ohta T, Soeji-ma H, Harada N, Abe K, Niikawa N: Ring chromosome 15 involving deletion of the insulin-like growth factor 1 receptor gene in a patient with features of Silver-Russell syndrome. Clin Dysmorphol 1993;2: 106-113.
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An interstitial deletion of proximal 8q (Q 11 — q 13) in a girl w'ith Silver-Russell syndromelike features
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Schinzel AA, Robinson WP, Binkert F, Fanconi A: An interstitial deletion of proximal 8q (q 11 — q 13) in a girl w'ith Silver-Russell syndromelike features. Clin Dysmorphol 1994;3:63-69.
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Asymmetry, short stature and variations of sexual development: A syndrome of congenital malformation
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Adolescent growth and pubertal progression in Silver-Russell syndrome
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