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- 2003
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Mark
Severe hypophosphatasia: Characterization of fifteen novel mutations in the ALPL gene
(
- Contribution to journal › Article
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Mark
Islet cell autoantibodies in cord blood from children with blood group incompatibility or hyperbilirubinemia.
(
- Contribution to journal › Article
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Mark
Islet autoantibodies in cord blood from patients who developed type 1 diabetes mellitus at 15-30 years of age.
(
- Contribution to journal › Article
- 2002
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Mark
Enterovirus Infection During Pregnancy is Not a Risk Factor for Celiac Disease in the Offspring.
(
- Contribution to journal › Article
-
Mark
An androgen receptor gene mutation (E653K) in a family with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency as well as in partial androgen insensitivity.
(
- Contribution to journal › Article
- 2001
-
Mark
Prediction of silent celiac disease at diagnosis of childhood type 1 diabetes by tissue transglutaminase autoantibodies and HLA
(
- Contribution to journal › Article
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Mark
Functional consequences of mutations in the MODY4 gene (IPF1) and coexistence with MODY3 mutations
(
- Contribution to journal › Article
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Mark
Analysis of short stature homeobox-containing gene ( SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity
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- Contribution to journal › Article
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Mark
Comparison of some different methods for analysis of thyroid autoantibodies: Importance of thyroglobulin autoantibodies
(
- Contribution to journal › Article
-
Mark
Secondary maternal cytomegalovirus infection - A significant cause of congenital disease
(
- Contribution to journal › Letter