Zobrazeno 1 - 10
of 143
pro vyhledávání: '"Klujber, L."'
Publikováno v:
Human Heredity, 1969 Jan 01. 19(5), 567-572.
Externí odkaz:
https://www.jstor.org/stable/45100673
Autor:
Klujber, L., Cholnoky, P.
Publikováno v:
Human Heredity, 1969 Jan 01. 19(1), 100-102.
Externí odkaz:
https://www.jstor.org/stable/45100776
Publikováno v:
Clinical Genetics. 6:155-159
An 18-month-old patient with juvenile hypophosphatasia and cleidocranial dysostosis is reported. Fifty-three of the 83 members of the family were examined biochemically, and among these were found four homozygotes and 25 heterozygotes for hypophospha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e0ef39a80779d5c3e52521867152931
https://doi.org/10.1111/j.1399-0004.1974.tb00645.x
https://doi.org/10.1111/j.1399-0004.1974.tb00645.x
Publikováno v:
American Journal of Mental Deficiency; Sep1980, Vol. 85 Issue 2, p120-128, 9p, 7 Charts
Publikováno v:
Diabetologia; Jan1988, Vol. 31 Issue 1, p30-34, 5p
Autor:
Klujber, L., Molnár, D., Kardos, M., Jászai, V., Soltész, Gy., Mestyán, J., Molnár, D, Jászai, V, Soltész, G, Mestyán, J
Publikováno v:
European Journal of Pediatrics; 1979, Vol. 132 Issue 4, p289-297, 9p
Publikováno v:
Acta Paediatrica; Jun1990, Vol. 79 Issue 6/7, p577-580, 4p
Publikováno v:
Clinical Genetics; Jan1972, Vol. 3 Issue 1, p60-66, 7p
Publikováno v:
Human Heredity. 19:567-572
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac37bb3d7b75678fb9df19baa725a67f
https://doi.org/10.1159/000152267
https://doi.org/10.1159/000152267
Publikováno v:
Biology of the Neonate; January 1972, Vol. 20 Issue: 3-4 p196-213, 18p