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The articulation of noncomplementarity in parental interaction and cognitive functioning in schizophrenic and non-schizophrenic patients /Valcov, Allen William January 1967 (has links)
No description available.
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Resource use of low-income families and its relationship to family patterns of adjustment to chronic maternal illness /Bardwell, Ann Skinner January 1968 (has links)
No description available.
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A concept of the family in colonial America : the Pembertons of Philadelphia /DiStefano, Judy Mann January 1971 (has links)
No description available.
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Interaction testing in the measurement of marital disturbance /Reddy, Michael Joseph January 1971 (has links)
No description available.
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Household and community in Canouan, British West Indies.Landman, Bette Emeline January 1972 (has links)
No description available.
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The effect of family-centered versus wife-centered obstetrical care upon famly life /Steiner, Joseph R. January 1972 (has links)
No description available.
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Families of working mothers in Puerto Rico /Quiñones RodriÌguez, Carmen F. January 1976 (has links)
No description available.
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Family's rules about affect and their relationship to the family's adjustment /Middelberg, Carol V. January 1978 (has links)
No description available.
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The effects of short-term intensive training on family communication skills /Mitchell, Carolyn Beth January 1979 (has links)
No description available.
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DNA Haplotypes Determination for Members of Families with Phenylketonuria (PKU) / DNA Haplotypes DeterminationQureshi, Afzal Mohammed 11 1900 (has links)
Phenylalanine hydroxylase deficiency causes phenylketonuria (PKU) in humans. PKU is a recessive genetic disease that affects 1 in 10000 births among the Caucasian population. Its gene locus is highly polymorphic in its DNA sequence among different individuals and patients with PKU. DNA polymorphisms at the PAH gene locus are used to obtain haplotypes through restriction enzyme analysis. So far forty-six distinct RFLP haplotypes have been discovered in the human population. In theory, 384 distinct RFLP haplotypes can exist. This project is to develop a program to assist the geneticists by obtaining haplotypes for each member of the PKU family. It uses information obtained from digestion of the DNA samples from the family members with the restriction enzymes. The restriction enzymes employed for this purpose are Pvuii, Bglii, EcoRI, Mspi, Xmni, Hindiii, and EcoRV. The program "PKU" generates all possible haplotypes for each member of the PKU family. The generated haplotypes may include haplotypes from the forty-six defined haplotypes list or from the 338 other haplotypes that may fit the description from the restriction enzyme analysis. The program then carries out an elimination phase during which the "extra" haplotypes that had been generated for the family members but whose presence was not supported by the data from the other family members are eliminated from the individuals' haplotype lists. The remaining haplotypes are then used to determine a sibling's carrier status of the PKU disease, i.e., whether or not a sibling is a carrier of the PKU disease. / Thesis / Master of Science (MS)
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