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Research article

First published 2009-11

A Case of Holoprosencephaly and 13q Deletion

Ultrasound

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Other

First published 2007-09

Expansion of the Deletion 13q Syndrome Phenotype: A Case Report

Eboni I. Lance, Barbara R. DuPont, Kenton R. Holden

Journal of Child Neurology

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Research article

First published 2005-11

Genetic Haploinsufficiency as a Phenotypic Determinant of a Deletion 13q Syndrome

Armen G. Kasyan, Kurt Benirschke

Pediatric and Developmental Pathology

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Case report

First published 2012-9

13q Deletion syndrome and retinoblastoma in identical dichorionic diamniotic monozygotic twins

Sonia De Francesco, Paolo Galluzzi, Alessandra Del Longo [...]

European Journal of Ophthalmology

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Case report

First published 2013-9

Retinoblastoma with Unusual Association of Postaxial Polydactyly

Deepak Mishra, Pratyush Ranjan, Bibhuti P. Sinha [...]

European Journal of Ophthalmology

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Research article

First published 1985-4

11p13 Deletion and Reduced RBC Catalase in a Patient with Aniridia,Glaucoma and Bilateral Wilms’ Tumor

Cosimo Barletta, Manuel Adolfo Castello, Enzo Ferrante [...]

Tumori Journal

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Research article

First published 1998-7

Lack of BRCA2 alterations in primary head and neck squamous cell carcinoma

H. Myra Nawroz-Danish, Wayne M. Koch, William H. Westra [...]

Otolaryngology–Head and Neck Surgery

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Review article

First published 2016-2

Retinoblastoma

Michael V. Ortiz, Ira J. Dunkel

Journal of Child Neurology

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Research article

First published 2002-3

Unusual Variant of Holoprosencephaly in Monosomy 13q

Pascale Marcorelles, Philippe Loget, Catherine Fallet-Bianco [...]

Pediatric and Developmental Pathology

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Research article

First published 1989-8

Genomic Alterations in Human Breast Cancer: A Review

Renato Mariani-Costantinl, Giorgio Merlo, Luigi Frati

Tumori Journal

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