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Publications by G C Geilen

Cathepsin a Deficiency in Galactosialidosis: Studies of Patients and Carriers in 16 Families

Pediatric Research
Child HealthPediatricsPerinatology
1996English

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Acid Carboxypeptidase Deficiency in Galactosialidosis

Japanese journal of human genetics
1991English

HLA and Hormonal Studies in Families of Patients With 21-Hydroxylase Deficiency - Cryptic Patients?

Pediatric Research
Child HealthPediatricsPerinatology
1981English

Compound Heterozygous SPATA5 Variants in Four Families and Functional Studies of SPATA5 Deficiency

European Journal of Human Genetics
Genetics
2018English

Cathepsin E Deficiency Impairs Autophagic Proteolysis in Macrophages

PLoS ONE
Multidisciplinary
2013English

Galactosialidosis

2020English

Interest of Individuals From BRCA Families to Participate in Research Studies Focused on Male BRCA Carriers

Familial Cancer
Cancer ResearchOncologyGenetics
2013English

Genomic Studies in Fragile X Premutation Carriers

Journal of Neurodevelopmental Disorders
PediatricsCognitive NeurosciencePerinatologyNeurologyForensic MedicineChild HealthPathology
2014English

Myophosphorylase Deficiency (McArdle's Disease) in Two Interrelated Families

Journal of Neurology, Neurosurgery and Psychiatry
PsychiatryMental HealthNeurologySurgery
1973English

Studies in Deficiency Disease

JAMA - Journal of the American Medical Association
Medicine
1948English

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