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B. Kerr

Boston Children's Hospital

5

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525

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Distinctive neurological phenotype associated with partial trisomy of chromosome 16

2013 European Journal of Paediatric Neurology
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The Clinical Phenotype of Costello Syndrome

2009
- B. Kerr
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Neurofibromatosis type 1 and sporadic optic gliomas

2002 Archives of Disease in Childhood
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Phenotypic variability and asymmetry of Rieger syndrome associated with PITX2 mutations

2000 Investigative Ophthalmology & Visual Science
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PHYSICAL MAPPING ACROSS THE FRAGILE X : HYPERMETHYLATION AND CLINICAL EXPRESSION OF THE FRAGILE X SYNDROME

1991 Cell
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Citations (307)