Chromosome Abnormalities in a Child with Down's Syndrome and in its Father
Open Access
- 1 January 1962
- journal article
- research article
- Published by Japan Academy in Proceedings of the Japan Academy
- Vol. 38 (8) , 526-530
- https://doi.org/10.2183/pjab1945.38.526
Abstract
Japan's largest platform for academic e-journals: J-STAGE is a full text database for reviewed academic papers published by Japanese societiesThis publication has 11 references indexed in Scilit:
- DIFFERENTIAL TRANSMISSION OF DOWN'S SYNDROME (MONGOLISM) THROUGH MALE AND FEMALE TRANSLOCATION CARRIERSThe Lancet, 1961
- CHROMOSOME STUDIES IN DETECTION OF PARENTS WITH HIGH RISK OF SECOND CHILD WITH DOWN'S SYNDROMEThe Lancet, 1961
- A MALE MONGOLOID WITH 46 CHROMOSOMESThe Lancet, 1961
- TRANSLOCATION-CARRYING PHENOTYPICALLY NORMAL MALES AND THE DOWN SYNDROMEThe Lancet, 1961
- 21-TRISOMY/NORMAL MOSAICISMThe Lancet, 1961
- CHROMOSOME TRANSLOCATION AS A CAUSE OF FAMILIAL MONGOLISMThe Lancet, 1960
- CHROMOSOMAL TRANSLOCATIONS IN MONGOLISM AND IN NORMAL RELATIVESThe Lancet, 1960
- CHROMOSOMAL ABNORMALITIES IN FATHER AND MONGOL CHILDThe Lancet, 1960
- Chromosome Studies in Ten Cases of MongolismProceedings of the Japan Academy, 1960
- THE SOMATIC CHROMOSOMES IN MONGOLISMThe Lancet, 1959