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Publications by L Neidengard

Craniosynostosis and Syndactyly: Expanding the 11q-- Chromosomal Deletion Phenotype.

Journal of Medical Genetics
Genetics
1980English

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Expanding the Phenotype Half of the Genotype−phenotype Space

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The 11q Terminal Deletion Disorder Jacobsen Syndrome Is a Syndromic Primary Immunodeficiency

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Marshall-Smith Syndrome: The Expanding Phenotype.

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PNPO Deficiency and Cirrhosis: Expanding the Clinical Phenotype?

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Expanding the ADCY5 Phenotype Toward Spastic Paraparesis

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Genetic Instability and Intratumoral Heterogeneity in Neuroblastoma With MYCN Amplification Plus 11q Deletion

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GP73 the Phenotype of 8p23 Deletion Syndrome

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Expanding the Distinctive Neuroimaging Phenotype of ACTA2 Mutations

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A Large Turkish Kindred With Syndactyly Type II (Synpolydactyly). 2. Homozygous Phenotype?

Journal of Medical Genetics
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1995English

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