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Clinical Genetics|October 1, 1981
The significance of different types of information in calculating the probability that a female relative of a Duchenne muscular dystrophy patient is a carrierL P ten Kate, P J OffringaNederlands Tijdschrift Voor Geneeskunde|August 12, 2006
[Rapid prenatal diagnosis of chromosomal abnormalities; limitations and possibilities]L P ten KateAmerican Journal of Medical Genetics|June 1, 1992
Completeness of catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypesL P ten KateAnnals of Human Genetics|January 1, 1977
A method for analysing fertility of heterozygotes for autosomal recessive disorders, with special reference to cystic fibrosis, Tay-Sachs disease and phenylketonuriaL P Ten KateJournal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|May 1, 1978
Evaluation of the enzymatic ammonia method for urine on the Du Pont automatic clinical analyzerF R Hindriks, A GroenClinical Genetics|July 1, 1983
Family distances can reveal hidden consanguinityL P ten Kate, R Rutgers-JanssenNederlands Tijdschrift Voor Geneeskunde|January 25, 1997
[Why the incidence of congenital and hereditary disorders usually is zero]M C Cornel, L P ten KatePageof 11