L. I v. E. T. R.

155 Misc. 2d 74
CourtNew York City Family Court
DecidedJuly 17, 1992
StatusPublished
Cited by1 cases

This text of 155 Misc. 2d 74 (L. I v. E. T. R.) is published on Counsel Stack Legal Research, covering New York City Family Court primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
L. I v. E. T. R., 155 Misc. 2d 74 (N.Y. Super. Ct. 1992).

Opinion

OPINION OF THE COURT

Sheldon M. Rand, J.

The interesting issue presented by respondent’s motion to dismiss this paternity petition is whether petitioner should be permitted to challenge the results of HLA and DNA tests, which exclude respondent as the father, when the child was born with a genetic condition which she might have inherited from respondent.

FACTS

This paternity action was commenced by petitioner mother [75]*75on May 28, 1991, wherein she claims that respondent is the father of her daughter. The child was born on March 1, 1990. From the time of the child’s birth until shortly before this proceeding, petitioner states that respondent supported the child. Thereafter, his support ceased. On July 12, 1991, respondent denied the allegations of paternity and obligations of financial support before Hearing Examiner Francine Seiden. Respondent, petitioner, and the child were ordered to submit to blood genetic marker tests. Both human leucocyte antigen (HLA) and deoxyribonucleic acid (DNA) probe analyses were conducted.

On December 3, 1991, the parties appeared in court and were given copies of the HLA and DNA test reports. Both reports excluded respondent as being the biological father of petitioner’s child. Petitioner advised the Hearing Examiner that she sought to challenge the results of the tests. The case was then sent to an Assignment Part for trial. On April 8, 1992, the parties appeared before this court, and the case was adjourned until June 12, 1992. On June 12, petitioner was served with the instant motion to dismiss this paternity action pursuant to Family Court Act § 5411 and CPLR 3211.2

[76]*76CONTENTIONS OF THE PARTIES

Respondent argues that dismissal is appropriate because the conclusiveness of DNA and HLA test results excluding paternity cannot be overcome by petitioner’s speculation that the test results are wrong. He claims that since both tests exclude paternity, there is simply no basis to challenge the results. While questions may exist surrounding the conclusiveness of blood test results regarding inclusiveness — that is — results which establish the probability of paternity, respondent argues that no questions exist regarding the conclusiveness of test results which exclude paternity.

Petitioner, however, alleges that objective evidence exists to support her claim that respondent is indeed the father of her child. According to an affidavit submitted by the child’s pediatrician, the child was born with an inherited condition known as polydactyly. Polydactyly is defined as the presence of more than five digits on either hand or foot. (Steadman’s Medical Dictionary [22d ed 1972].) Upon consultation with the pediatrician, petitioner claims that she was told that polydactyly is genetic, and that it is typically seen in at least one parent of a child born with the condition. When petitioner informed respondent of the child’s condition, he allegedly claimed that, he, too, was born with extra fingers and toes. According to petitioner, this information served as confirmation that the child was respondent’s. Given these circumstances, petitioner argues that to dismiss the case at this juncture, in the absence of a fact-finding hearing, would be error. She claims that such an order would preclude her from challenging the results of blood tests which are at odds with the genetic condition purportedly shared by the respondent and child.

LAW

(A) Background

Family Court Act § 532 provides for the admissibility of blood grouping tests in paternity proceedings to aid in ascertaining whether the alleged father is or is not the biological father of the child. The HLA test is a biochemical test which utilizes blood groups, serum proteins, and white and red blood cell enzymes to analyze the characteristics of a mother, child and putative father (Matter of Beaudoin v Tilley, 110 Misc 2d [77]*77696). Rather than being used solely for exclusionary purposes, HLA and related blood tests can increase the probability of exclusion to such a degree as to affirmatively prove paternity (Matter of A. T. v M. K., 145 Misc 2d 525; Matter of Department of Social Servs, v Thomas J. S., 100 AD2d 119 [2d Dept 1984]).3

The DNA probe, as a genetic blood marker test, is likewise admissible in paternity proceedings under Family Court Act § 532. (Matter of A. T. v M. K., supra; Matter of Baby Girl S., 140 Misc 2d 299 [Sur Ct, NY County 1988].) DNA testing is founded on the premise that each individual possesses his own genetic signature. (People v Wesley, 140 Misc 2d 306.) The DNA chain of every person is comprised of breaks, or " 'stutters’ ” which exist in a repetitive pattern throughout the DNA molecule. (1 Schatkin, Disputed Paternity Proceedings §5.11, at 5-8 [4th rev ed (1992 Supp Pamph)].) In DNA fingerprinting, a small sample of blood is taken from the mother, putative father and child. Cells containing the DNA are then extracted. An enzyme is added to fragment the DNA,4 and the result of the process is a DNA fingerprint, much like a bar code appearing on retail products. (1 Schatkin, op. cit., § 5.11, at 5-8.) Each bar in the child’s code is attributable to either the biological mother or biological father. "[T]he examination begins with a comparison of the child’s DNA fingerprint with the mother’s, and the location of all bars which match the mother’s code. The man will then be [78]*78positively identified as the father if every remaining code of the child matches with a code of the putative father. If he is not the father, very few of the bars will match”. (1 Schatkin, op. cit., § 5.11, at 5-8.) By permitting blood genetic marker tests as inclusory evidence pursuant to Family Court Act § 532, courts have acknowledged the accuracy of such tests and their probative value in paternity cases.5 (Matter of A. T. v M. K., supra, at 529.)

B. Analysis

Petitioner’s ultimate burden is to establish paternity by clear and convincing evidence, which is entirely satisfactory, and which creates a genuine belief that respondent is the biological father. (Matter of Commissioner of Social Servs. v Philip De G., 59 NY2d 137, 141-142; Matter of Jane PP v Paul QQ, 65 NY2d 994; Matter of Kimiecik v Jesse U., 111 AD2d 976 [3d Dept 1985].) Notwithstanding the weight accorded blood grouping tests in meeting that burden, it has been consistently held that such tests are not dispositive, and cannot be the sole basis for establishing paternity. (Matter of Julie UU. v Joseph W., 108 AD2d 1038 [3d Dept 1985]; Matter of Beaudoin v William HH., 157 AD2d 995 [3d Dept 1990].) Such tests are but one factor to be considered. (Matter of A. T. v M. K., supra, at 530; Matter of Department of Social Servs. v Thomas J. S., supra, at 124.) The court must weigh blood grouping evidence along with all other evidence in the case to arrive at the finding of paternity. (Matter of Commissioner of Social Servs. v Bart D., 121 Misc 2d 425 [Fam Ct, Kings County 1983]; Matter of Shirley R. v Ricardo B., 144 AD2d 472 [2d Dept 1988].)

Respondent claims that, while there may be arguable issues surrounding the conclusiveness of HLA and DNA results establishing the probability of paternity, such questions do not arise when the test results

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Bluebook (online)
155 Misc. 2d 74, Counsel Stack Legal Research, https://law.counselstack.com/opinion/l-i-v-e-t-r-nycfamct-1992.