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Seite 1 für „Hereditary“ · Literaturverweise aus öffentlichen Artikeln
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[Hereditary cerebellar aataxia with spinal muscular atrophies].
pubmed · 4104837
Literaturverweis öffnen[CDG (congenital disorders of glycosylation). Differential hereditary ataxia in adulthood diagnosis].
pubmed · 12242963
Literaturverweis öffnenHereditary angioneurotic Quincke's edema
pubmed · 3926548
Literaturverweis öffnenMouse models and translational research progress of hereditary vestibular dysfunction
pubmed · 42216666
Literaturverweis öffnenFear of cancer recurrence across sporadic, familial and hereditary breast cancer: the role of genetic risk and psychosocial factors
doi · 10.21203/rs.3.rs-9306007/v1
Literaturverweis öffnenHereditary Transthyretin Amyloidosis.
pubmed · 20301373
Literaturverweis öffnenParsonage-Turner Syndrome and Hereditary Brachial Plexus Neuropathy
pubmed · 38176820
Literaturverweis öffnenHereditary Pancreatitis
pubmed · 1582401
Literaturverweis öffnen[Malaria hypothesis--the significance of the hereditary red cell traits Hb S and glucose-6-phosphate dehydrogenase deficiency in malaria (author's transl)].
pubmed · 396227
Literaturverweis öffnenδβ Thalassemia and Hereditary Persistence of Fetal Hemoglobin
pubmed · 1713909
Literaturverweis öffnenComment on "Cerebral vascular malformation screening in hereditary hemorrhagic telangiectasia: Balancing low diagnostic yield against high-risk hemorrhage"
pubmed · 42202557
Literaturverweis öffnenHereditary galactosemia
pubmed · 29409891
Literaturverweis öffnen[Hereditary non-spherocytic hemolytic anemia caused by glucosephosphate isomerase deficiency: 1. case observed in Switzerland].
pubmed · 4419288
Literaturverweis öffnenParental non-hereditary teratogenic exposure factors on the occurrence of congenital heart disease in the offspring in the northeastern Sichuan, China
pubmed · 32127562
Literaturverweis öffnenA Rare Case of Hereditary Bone Dysplasia: Osteopoikilosis in a Mother and Her Son
pubmed · 38952582
Literaturverweis öffnenCase Report: The compound heterozygotes variants in FLT4 causes autosomal recessive hereditary lymphedema in a Chinese family
pubmed · 37035731
Literaturverweis öffnenCase 10: A patient with an isolated prolongation of the activated partial thromboplastin time without a bleeding problem – severe hereditary Factor XII deficiency
pubmed · 10517121
Literaturverweis öffnenGenotypic and Phenotypic Characteristics of Turkish Patients with Hereditary Fructose Intolerance
pubmed · 42164825
Literaturverweis öffnenInternalizing and Externalizing Problems and Psychiatric Comorbidities in Children With Hereditary Spherocytosis
pubmed · 42274394
Literaturverweis öffnenTwo novel variations p.(Ser1275Thr) and p.(Ser1275Arg) in FLT4 causing prenatal hereditary lymphedema type 1
pubmed · 36538874
Literaturverweis öffnenCase Report: Diagnostic challenge between epileptic seizure and tetany in Albright hereditary osteodystrophy
pubmed · 42294472
Literaturverweis öffnenEvaluation of Pathogenicity and Causativity of Variants in the MPZ and SH3TC2 Genes in a Family Case of Hereditary Peripheral Neuropathy
pubmed · 37372933
Literaturverweis öffnenCerebral vascular malformation screening in hereditary hemorrhagic telangiectasia: Balancing low diagnostic yield against high-risk hemorrhage
pubmed · 41713125
Literaturverweis öffnen[The molecular basis of hereditary persistence of fetal hemoglobin (HPFH). Clinical importance of the hemoglobin switching mechanism with special reference to Corfu delta beta zero thalassemia].
pubmed · 2464759
Literaturverweis öffnen[Hereditary dental hard tissue diseases]
pubmed · 26081863
Literaturverweis öffnenHereditary angioedema and the gastrointestinal tract
pubmed · 42021981
Literaturverweis öffnen