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Dyggve-Melchior-Clausen syndrome and Smith-McCort dysplasia: Clinical and molecular findings in three families supporting genetic heterogeneity in Smith-McCort dysplasia
by
Neumann, Luitgard M.
,
Ghouzzi, Vincent El
,
Paupe, Vincent
,
Weber, Hans-Peter
,
Fastnacht, Elisabeth
,
Leenen, Andreas
,
Lyding, Sigrid
,
Klusmann, Anne
,
Mayatepek, Ertan
,
Pelz, Jörg
,
Cormier-Daire, Valerie
Published in
American journal of medical genetics. Part A
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Evans Syndrome in a Patient with Chromosome 22q11.2 Deletion Syndrome: A Case Report
by
Kratz, Christian P.
,
Niehues, Tim
,
Lyding, Sigrid
,
Heusch, Andreas
,
Janssen, Gisela
,
Göbel, Ulrich
Published in
Pediatric hematology and oncology
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American Journal Of Medical Genetics Part A
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American Journal Of Medical Genetics. Part A
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Pediatr. Hematol. Oncol
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Pediatric Hematology And Oncology
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Adolescent
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Anemia, Hemolytic, Autoimmune - Drug Therapy
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Anemia, Hemolytic, Autoimmune - Genetics
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Atrophy
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Autoimmune Diseases - Drug Therapy
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Base Sequence
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Chromosome Deletion
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Chromosomes, Human, Pair 22 - Ultrastructure
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Wiley Online Library All Journals
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Taylor And Francis:jisc Collections:taylor And Francis Read And Publish Agreement 2024-2025:Medical Collection (Reading List)
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Wiley:jisc Collections:wiley Read And Publish Open Access 2024-2025 (Reading List)
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