DELETION ON SHORT ARMS OF A B-CHROMOSOME WITHOUT "CRI DU CHAT" SYNDROME.
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Chromosome Aberrations↗
Biomedical subjects
H BAITSCH
Publications and source records attributed to H BAITSCH.
ENHANCEMENT OF ERYTHROCYTE-GALACTOKINASE ACTIVITY IN LANGDON-DOWN TRISOMY.
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Down Syndrome↗
[ON FORMAL GENETICS OF PSUDOCHOLINESTERASE. STUDIES ON 408 FAMILIES].
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Cholinesterases↗
STUDIES ON FORMAL GENETICS OF THE PSEUDO-CHOLINESTERASE POLYMORPHISM; AN ATYPICAL SEGREGATION IN A FAMILY.
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Biomedical Research↗
[FAMILIAL OCCURRENCE OF AN ABNORMAL D-CHROMOSOME].
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Chromosome Aberrations↗
ON NOMENCLATURE OF PSEUDOCHOLINESTERASE POLYMORPHISM.
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Apnea↗
[GAMMA GLOBULIN GROUPS GM AND INV AMONG THE POPULATION OF HONOLULU (HAWAII)].
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Biomedical Research↗
[ON THE MORPHOLOGY AND GENETICS OF GM POLYMORPHISM OF GAMMA GLOBULINS (CHARACTERISTICS OF GM(A), GM(B), GM(E); STUDY ON 387 FAMILIES].
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Biomedical Research↗
[CLINICAL ASPECTS AND GENETICS OF PSEUDOCHOLINESTERASES].
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Butyrylcholinesterase↗
[STUDIES ON THE GENETICS OF SERUM PROTEINS: THE GC FACTOR OF HIRSCHFELD AND ITS ALLELE INCIDENCE IN SOUTHWESTERN GERMANY].
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Alleles↗
Hereditary fructose intolerance. An inborn defect of hepatic fructose-1-phosphate splitting aldolase.
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Adipose Tissue↗
[THE GM AND INV SYSTEMS IN EUROPE].
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Blood Group Antigens↗
[Serum haptoglobin groups].
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Haptoglobins↗
[On the population genetics of allele frequency of haptoglobin blood groups in Europe and Oceania].
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Blood Group Antigens↗
[On the behavior of free fatty acids in the blood in childhood. I. The behavior of the fasting value in metabolically healthy children, in hypophysial dwarfism, in hypothyroidism and in prepuberal obesity].
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Child↗
[Mother-child examinations for forensic evidence on haptoglobin serum groups].
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Blood Group Antigens↗
[Haptoglobin types. Method of their determination, allele incidences in some random samples. 2].
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Alleles↗
[Haptoglobin types. Method of determination; allele incidences in some random samples. 1].
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Alleles↗