Defendant appeals as of right from a circuit court judgment finding that plaintiff is the father of a child born to defendant on July 14, 1978.
On August 13, 1979, plaintiff filed his paternity complaint, alleging that he was the father of defendant’s child, Kiela Nasha Payne, born out of wedlock on July 14, 1978. In her answer, defendant denied that plaintiff was the father of her child. Pursuant to the court’s order, upon plain *125 tiffs motion, plaintiff, defendant and the child submitted to human leukocyte antigen (HLA) testing in order to establish parentage.
At trial, plaintiff testified that he and defendant engaged in sexual intercourse on numerous occasions between August and November, 1977, inclusive. Plaintiff believes that he is the child’s father.
On the other hand, although defendant admitted having sexual relations with plaintiff, defendant testified that she and plaintiff quarreled in mid-September, 1977, and that she did not see or speak with plaintiff again until June, 1978. Defendant also testified that she had sexual relations with James Moore from mid-October until December, 1977.
James Moore acknowledged that he had sexual relations with defendant from mid-October until the end of the year. Moore believed that he was the child’s father.
Each side presented additional evidence favoring their own position. Critical evidence was presented by plaintiff through Richard H. Walker, M.D. Defendant unsuccessfully moved to exclude Dr. Walker’s testimony relative to the results of the blood and tissue-typing tests.
Dr. Walker conducted blood and tissue-type testing, including blood grouping, HLA, heptoglobin and sickle cell tests, on plaintiff, defendant and the child in May, 1980. Dr. Walker testified that, based on the blood grouping tests, it was impossible to exclude plaintiff from paternity. Dr. Walker described the remaining tests. The remaining tests involve isolation of genetic traits contained in blood, so-called "markers”. The greater the correlation between a child’s "markers” and a putative father’s "markers”, the greater the probability that the putative father is the biological father. *126 HLA testing began in the 1950’s and at that time was used primarily in tissue typing for organ transplants. The test involves the isolation of white blood cells from the blood. These cells are tested against different reagents to determine the "markers”. HLA testing is the most advanced system for obtaining paternity exclusions and, failing an exclusion, for giving a high probability of inclusion. Dr. Walker testified that, based on the test results, the probability that plaintiff was the father of defendant’s child, as compared to the probability that a random black man was the father, was 95.56%. The probability that plaintiff was the father, as opposed to a random white man, was 99.8%.
The parties stipulated that defendant’s last menstrual period ended on October 6, 1977. Dr. Walker indicated that generally the most fertile time for conception occurs approximately two weeks after the first day of the last menstrual period. In defendant’s case, however, conception could have occurred prior to the last menstrual period or as late as the first week of November, 1977.
At the close of proofs, the trial court concluded that plaintiff was the child’s father. The court relied heavily but not exclusively on the test results, and the paternity determination was expressly made under the Child Custody Act, MCL 722.21 et seq.; MSA 25.312(1) et seq.
A threshold question in this case is whether the trial court could determine paternity under the Child Custody Act.
Paternity proceedings are of a purely statutory nature.
McFetridge v Chiado,
The next question for this Court to address is whether reversible error occurred by the admission of the HLA test results.
At the time of trial, the results of blood tests were receivable into evidence only in cases where a definite exclusion was established. MCL 722.716(d); MSA 25.496(d) prior to its amendment by
"(1) In a proceeding under this act before trial, the court, upon application made by or on behalf of either party, or on its own motion, shall order that the mother, child, and alleged father submit to blood or tissue typing tests which may include, but are not limited to, tests of red cell antigens, red cell isoenzymes, human leukocyte antigens, and serum proteins to determine whether the alleged father is likely to be, or is not, the father of the child.
*128 "(4) The result of a blood or tissue typing test, and if a determination of exclusion of paternity cannot be made, a calculation of the probability of paternity made by a person the court determines is qualified as an examiner of blood or tissue types based on the result of a blood or tissue typing test shall be admissible in evidence in the trial of the case.” MCL 722.716; MSA 25.496 as amended by1982 PA 129 .
We are persuaded that the trial court did not reversibly err by admitting into evidence in this case the HLA test results.
HLA testing is distinguishable from blood group testing in significant respects. Unlike ABO testing, HLA testing is a "potentially powerful tool in determining the probability of paternity”. See
Varney v
Young;
In reaching our decision, we have noted the case, cited by defendant, of
Klein v Franks,
In affirming this case, we note that we do not decide whether the evidence would have been admissible in a case where the mother, in bringing a paternity action against the putative father, sought to introduce evidence of HLA test results. That case is not before us.
Affirmed.
