Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …
Proceedings of the National Academy of Sciences, 1983 - National Acad Sciences
The clinical, radiological, and pathological findings in three siblings affected with the
autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …
autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …
Carbonic Anhydrase II Deficiency Identified as the Primary Defect in the Autosomal Recessive Syndrome of Osteopetrosis with Renal Tubular Acidosis and Cerebral …
WS Sly, D Hewett-Emmett, MP Whyte, YSL Yu… - Proceedings of the …, 1983 - JSTOR
The clinical, radiological, and pathological findings in three siblings affected with the
autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …
autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …
Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …
WS Sly, D Hewett-Emmett, MP Whyte, YS Yu… - Proceedings of the …, 1983 - cir.nii.ac.jp
抄録< jats: p> The clinical, radiological, and pathological findings in three siblings affected
with the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and …
with the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and …
Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …
WS Sly, D Hewett-Emmett, MP Whyte… - Proceedings of the …, 1983 - ncbi.nlm.nih.gov
The clinical, radiological, and pathological findings in three siblings affected with the
autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …
autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …
[引用][C] Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …
WS SLY, D HEWETT-EMMETT… - Proceedings of the …, 1983 - pascal-francis.inist.fr
Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive
syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification (erythrocytes/bone …
syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification (erythrocytes/bone …
Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …
WS Sly, D Hewett-Emmett, MP Whyte… - Proceedings of the …, 1983 - ui.adsabs.harvard.edu
The clinical, radiological, and pathological findings in three siblings affected with the
autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …
autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …
Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …
WS Sly, D Hewett-Emmett, MP Whyte… - Proceedings of the …, 1983 - europepmc.org
The clinical, radiological, and pathological findings in three siblings affected with the
autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …
autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …
Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …
WS Sly, D Hewett-Emmett, MP Whyte, YS Yu… - 1983 - profiles.wustl.edu
The clinical, radiological, and pathological findings in three siblings affected with the
autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …
autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …
Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …
WS Sly, D Hewett-Emmett, MP Whyte… - Proceedings of the …, 1983 - pubmed.ncbi.nlm.nih.gov
The clinical, radiological, and pathological findings in three siblings affected with the
autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …
autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …
[PDF][PDF] Carbonic anhydrase II deficiency-identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …
WS SLY, D HEWETT-EMMETT, P WHYTE… - Proc. Nati Acad. Sci …, 1983 - researchgate.net
Theclinical, radiological, and pathological findings in three siblings affected with the
autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …
autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral …