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1 Ergebnisse
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Human ABL1 deficiency syndrome (HADS) is a recognizable syn..:
AlAbdi, Lama
;
Neuhann, Teresa
;
Prott, Eva-Christina
...
Human Genetics. 143 (2024) 6 - p. 739-745 , 2024
Link:
https://doi.org/10.1007/s00439-024-02677-y
RT Journal T1
Human ABL1 deficiency syndrome (HADS) is a recognizable syndrome distinct from ABL1-related congenital heart defects and skeletal malformations syndrome
UL https://suche.suub.uni-bremen.de/peid=cr-10.1007_s00439-024-02677-y&Exemplar=1&LAN=DE A1 AlAbdi, Lama A1 Neuhann, Teresa A1 Prott, Eva-Christina A1 Schön, Ulrike A1 Abdulwahab, Firdous A1 Faqeih, Eissa A1 Alkuraya, Fowzan S. PB Springer Science and Business Media LLC YR 2024 SN 0340-6717 SN 1432-1203 JF Human Genetics VO 143 IS 6 SP 739 OP 745 LK http://dx.doi.org/https://doi.org/10.1007/s00439-024-02677-y DO https://doi.org/10.1007/s00439-024-02677-y SF ELIB - SuUB Bremen
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