Author: "Yntema, H.G." / Topic: opheldering van erfelijke ziekten en hun moleculaire diagnostiek. - Searchworks@Jio Institute Digital Library Search Results

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Your search keyword '"Yntema, H.G."' showing total 4 results

Start Over Author "Yntema, H.G." Topic opheldering van erfelijke ziekten en hun moleculaire diagnostiek.

4 results on '"Yntema, H.G."'

1. In-frame deletion in MECP2 causes mild nonspecific mental retardation.

Author: Yntema, H.G. and Yntema, H.G.
Subjects: Elucidation of hereditary disorders and their molecular diagnosis., Opheldering van erfelijke ziekten en hun moleculaire diagnostiek.
Published: 2002

2. Low frequency of MECP2 mutations in mentally retarded males.

Author: Yntema, H.G. and Yntema, H.G.
Subjects: Elucidation of hereditary disorders and their molecular diagnosis., Opheldering van erfelijke ziekten en hun moleculaire diagnostiek.
Published: 2002

3. Expanding phenotype of XNP mutations: mild to moderate mental retardation.

Author: Yntema, H.G. and Yntema, H.G.
Subjects: Elucidation of hereditary disorders and their molecular diagnosis., Opheldering van erfelijke ziekten en hun moleculaire diagnostiek.
Published: 2002

4. Molecular genetics of nonspecific x-linked mental retardation.

Author: Yntema, H.G. and Yntema, H.G.
Subjects: Elucidation of hereditary disorders and their molecular diagnosis., Opheldering van erfelijke ziekten en hun moleculaire diagnostiek.
Published: 2001

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