Human Genetics: Proceedings of the Fifth International Congress of Human Genetics, Mexico City, 10-15 October 1976Excerpta Medica, 1977 - 408 Seiten |
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Seite 117
... normal . Laparoscopy was performed and revealed ovaries of normal size on both sides . Biopsies showed a fibrous cortical zone with primordial follicles . The second patient was a typical case of Klinefelter's syndrome and was examined ...
... normal . Laparoscopy was performed and revealed ovaries of normal size on both sides . Biopsies showed a fibrous cortical zone with primordial follicles . The second patient was a typical case of Klinefelter's syndrome and was examined ...
Seite 220
... Normal 21,776 2 0 Normal 966 1 0 Normal 23,184 4 0 Normal 1,082 0 0 Normal < 10 days 3,241 0 0 Normal 1 month 0 0 0 Normal < 10 days 5,496 0 1 month 509 0 OO 0 Normal Normal ( Beutler ) The procedures used are described by Shih ( 1973 ) ...
... Normal 21,776 2 0 Normal 966 1 0 Normal 23,184 4 0 Normal 1,082 0 0 Normal < 10 days 3,241 0 0 Normal 1 month 0 0 0 Normal < 10 days 5,496 0 1 month 509 0 OO 0 Normal Normal ( Beutler ) The procedures used are described by Shih ( 1973 ) ...
Seite 397
... normal concentration in serum is approximately 2 mg / ml , which inhibit 0.6 to 0.8 mg of active trypsin . The original observation of the deficiency was that there were a few rare individuals with levels of about 15 % of the normal ...
... normal concentration in serum is approximately 2 mg / ml , which inhibit 0.6 to 0.8 mg of active trypsin . The original observation of the deficiency was that there were a few rare individuals with levels of about 15 % of the normal ...
Inhalt
The legal aspects of genetic screening and counseling | 3 |
Some trends in the study of spontaneous and induced mutation in | 19 |
Temporal genes and developmental programs | 33 |
Urheberrecht | |
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aberrations Acad activity alleles Amer amniocentesis amniotic fluid amniotic fluid cells analysis antenatal antigens assay autosomal banding biochemical blood group Bodmer cancer cell hybridization chromatid chromosome abnormalities clinical clones congenital correlation culture cytogenetic deficiency detected determined differentiation disease disorders donor Down's syndrome Editors environmental enzyme errors of metabolism extinction factors fetal fetus fibroblasts frequency functions Galjaard gene genetic distance genome H-2 complex hemoglobin HLA-D Human Genetics inborn errors individuals inheritance involved karyotype lactose Lancet linkage disequilibrium loci locus lymphocytes malformations marker maternal methods microcell Milunsky mouse mutagens mutation rates Nature Lond neural tube defects newborns normal observed parents patients phenotype phenylketonuria polymorphism population genetics possible pregnancies prenatal diagnosis Press Proc protein recent risk Ruddle samples selection somatic cell specific structural studies suggested Table techniques tissue translocation tumors variants X chromosome Zinkernagel