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American journal of human genetics, 2019-05, Vol.104 (5), p.957-967
- Van Esch, Hilde
- Colnaghi, Rita
- Freson, Kathleen
- Starokadomskyy, Petro
- Zankl, Andreas
- Backx, Liesbeth
- Abramowicz, Iga
- Outwin, Emily
- Rohena, Luis
- Faulkner, Claire
- Leong, Gary M.
- Newbury-Ecob, Ruth A.
- Challis, Rachel C.
- Õunap, Katrin
- Jaeken, Jacques
- Seuntjens, Eve
- Devriendt, Koen
- Burstein, Ezra
- Low, Karen J.
- O’Driscoll, Mark
2019
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The New England journal of medicine, 2010-10, Vol.363 (18), p.1774; author reply 1774
2010
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Annals of neurology, 2010-08, Vol.68 (2), p.259-263
2010
Link zum Volltext
The New England journal of medicine, 2010-10, Vol.363 (18), p.1774-1775
2010
Link zum Volltext
The Lancet (British edition), 1994-10, Vol.344 (8931), p.1234-1235
1994
Link zum Volltext
Pediatric research, 1994-07, Vol.36 (1), p.46-46A
1994
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Nature genetics, 1997-05, Vol.16 (1), p.88-92
1997
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American journal of human genetics, 1998-03, Vol.62 (3), p.542-550
1998
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Human mutation, 1999, Vol.13 (3), p.197-202
1999
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Journal of inherited metabolic disease, 2010-08, Vol.33 (4), p.451-451
2010
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European journal of human genetics : EJHG, 1998-03, Vol.6 (2), p.99-104
1998
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Evidence for Genetic Heterogeneity in the Carbohydrate-Deficient Glycoprotein Syndrome Type I (CDG1)
1996
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