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 110
... Trisomy 6p Two patients with partial trisomy for 6p were first reported by Therkelsen et al . ( 1971 ) ( Therkelson , 1975 , personal communication ) . The clinical features ... Trisomy 8 As far as we can tell , trisomy 110 J. de Grouchy.
... Trisomy 6p Two patients with partial trisomy for 6p were first reported by Therkelsen et al . ( 1971 ) ( Therkelson , 1975 , personal communication ) . The clinical features ... Trisomy 8 As far as we can tell , trisomy 110 J. de Grouchy.
Seite 111
... Trisomy 8 As far as we can tell , trisomy 8 is an example of a different kind of situation . Most features of the syndrome correlated with trisomy for the entire chromosome can be TABLE 3 Dermatoglyphics in trisomy 8 , trisomy 8qter and ...
... Trisomy 8 As far as we can tell , trisomy 8 is an example of a different kind of situation . Most features of the syndrome correlated with trisomy for the entire chromosome can be TABLE 3 Dermatoglyphics in trisomy 8 , trisomy 8qter and ...
Seite 112
... trisomy 8 , trisomy 8p and trisomy 8qter ( after Rethoré , 1976 , unpublished observations ) . Trisomy 13 Trisomy 13 was one of the first cytogenetic syndromes to be described . In recent years , trisomy for the proximal half and ...
... trisomy 8 , trisomy 8p and trisomy 8qter ( after Rethoré , 1976 , unpublished observations ) . Trisomy 13 Trisomy 13 was one of the first cytogenetic syndromes to be described . In recent years , trisomy for the proximal half and ...
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