DNA-based prenatal diagnosis of the infantile form of neuronal ceroid lipofuscinosis (INCL, CLN1)-Reference-Cited by-同舟云学术

DNA-based prenatal diagnosis of the infantile form of neuronal ceroid lipofuscinosis (INCL, CLN1)

Published:1991-05 Issue:5 Volume:11 Page:323-328
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Järvelä Irma,Rapola Juhani,Peltonen Leena,Puhakka Lea,Vesa Jouni,Ämmälä Pirkko,Salonen Riitta,Ryynänen Markku,Haring Pertti,Mustonen Aki,Santavuori Pirkko

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference22 articles.

1. The Newfoundland aggregate of neuronal ceroid-lipofuscinosis

2. Clinical classification of neuronal ceroid-lipofuscinosis subtypes

3. THE ULTRASTRUCTURAL CHARACTERISTICS OF THE ABNORMAL CYTOSOMES IN BATTEN-KUFS' DISEASE

4. First-trimester diagnosis of juvenile neuronal ceroid lipofuscinosis by demonstration of fingerprint inclusions in chorionic villi

5. Batten disease (Spielmeyer-Vogt disease, juvenile onset neuronal ceroid-lipofuscinosis) gene (CLN3) maps to human chromosome 16

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1. MRI Of the Brain, EEG Sleep Spindles and SPECT in the Early Diagnosis of Infantile Neuronal Ceroid Lipofuscinosis;Developmental Medicine & Child Neurology;2008-11-12

2. The Neuronal Ceroid-Lipofuscinoses. Recent Advances;Brain Pathology;2006-04-05

3. Prenatal Diagnosis of Lysosomal Storage Diseases;Brain Pathology;2006-04-05

4. Pirkko Santavuori (1933-2004);Journal of Child Neurology;2004-06

5. 7 Molecular genetic testing for neuronal ceroid lipofuscinoses;Batten Disease: Diagnosis, Treatment, and Research;2001