Burnham, "Isoimmunization in pregnancy: its possible bearing on the etiology of erythroblastosis
foetalis," Journal of the American Medical Association, vol.
 Human genes: RBI, retinoblastoma 1; TP53, tumor protein p53; RUNX1T1, runt-related transcription factor 1, translocated to, 1 (cydin D-related) (formerly EFO); RUNXI, runt-related transcription factor 1; OUG2, oligodendrite lineage transcription factor 2; ERG, v-ets avian erythroblastosis
virus E26 oncogene homolog; TMPRSS2, transmembrane protease, serine 2; U2AFI, U2 small nuclear RNA auxiliary factor 1; BCL2, B-cell CLL/lymphoma 2.
In addition, the identification of prostate cancer specific genomic aberrations like the TMPRSS2:ERG gene fusion (transmembrane protease serine 2: Erythroblastosis
virus E26 oncogene-related gene) might improve diagnosis and affect prostate cancer treatment.
fetalis and congenital syphilis, as an enlarged spleen is more fragile than a normal organ.
Extrapyramidal cerebral palsy with hearing loss following erythroblastosis
The decreasing RBC, Ht, and Hb values indicate that RBCs are being destroyed by the leucocytosis in erythrocytic anaemia with subsequent erythroblastosis
The issue before the Court was whether the physicians could be held liable for erythroblastosis
fetalis (i.e., either Rh incompatibility disease or ABO incompatibility disease) suffered by a child due to the negligent transfusion of the mother nine years prior to the child's conception.
(hyperbilirubinemia[mh] OR erythroblastosis
, fetal[mh] OR anemia, hemolytic[mh]) AND immunoglobulins, intravenous[mh] AND infant, newborn[mh] You try adding in terms for the ABO incompatibility portion of the question from Table 1, but you notice that doing so seems to screen out quite a bit of material, leading you to suspect that you may be risking omitting relevant information, and you return to the broader search strategy.
In the early 1950's, he was the first physician in Worcester County to do exchange transfusions for newborn babies born with erythroblastosis
Differential Diagnosis Jaundice appearing at birth or within 24 hours: sepsis, Erythroblastosis
retails, concealed hemorrhage, cytomegalic inclusion disease, rubella, congenital toxoplasmosis.
Gene name U60145 Fragile X mental retardation 1 X67108 Brain derived neurothrophic factor L20682 Erythroblastosis
virus E26 oncogene homolog 1 (avian) M12492 Type IIb subunit of cAMPdependent protein kinase U09401 Tenascin C M31178 Calbindin 1 M85301 Solute carrier family 9, member 4 M35162 Gamma-aminobutyric acid A receptor, delta S39221 N-methyl-D-aspartate receptor U89514 Calpain 9 AA866238 Similar to Acyl carrier protein, mitochondrial precursor U90271 CD152 antigen AB019576 Timeless (Drosophila) homolog Z22607 Bone morphogenetic protein 4 AF083331 Kinesin family member IB A1639073 Similar to Cadherin-related neuronal receptor Acc.