Use of phenylketonuria in Sentences. 19 Examples
The examples include phenylketonuria at the start of sentence, phenylketonuria at the end of sentence and phenylketonuria in the middle of sentence
For urdu meanings and examples of phenylketonuria click here
phenylketonuria at the end of sentence
- Objective To study the method for gene diagnosis of phenylketonuria.
- Objective To establish a simple, accurate and rapid method for screening of the mutant genes in phenylketonuria.
- Conclusion:The special bone changes in phenylketonuria were important X-ray signs suggestive of phenylketonuria.
- This result showed that PCR-SSCP analysis could be effectively used for the direct gene diagnosis of phenylketonuria.
- Separating Amino Acids in Blood and Urine by Microcrystalline Cellulose Film Chromatography - To ldentify phenylketonuria.
- Objective To establish a method with high efficiency in detecting phenylalanine hydroxylase(PAH) gene mutations and hence to rapidly diagnose prenatal fetals with phenylketonuria .
phenylketonuria in the middle of sentence
- In other words, children with phenylketonuria can and should have a normal productive life.
- Samples obtained through screening programme for phenylketonuria and congenital hypothyroidism.
- Objective To describe the incidence of congenital hypothyroidism(CH)and phenylketonuria(PKU)in Maanshan city.
- To explore the morbidity of Congenital hypothyroidism(CH) and phenylketonuria(PKU) among newborn in Heze city.
- To explore the morbidity Congenital hypothyroidism ( CH ) and phenylketonuria ( PKU ) among newborn in Heze city.
- The management of phenylketonuria in childhood requires a multidisciplinary approach across the hospital community interface.
- Tragically, their daughter Carol was born in 1920 with a genetic birth defect called phenylketonuria, which led to mental impairment.
- Objective To establish a simple[sentence dictionary], accurate and rapid method for screening of the mutant genes in phenylketonuria (PKU).
- To understand the prevalence of thyroid hypofunction(CH) and phenylketonuria(PKU) among newborn in Penglai in order to find and treat them in time.
- Objective To explore the incidence and distribution features of neonatal phenylketonuria(PKU) and congenital hypothyroidism(CH) in Lianyungang area.
- Objective To investigate the point mutation features of exon 11 and 12 in phenylalanine hydroxylase( PAH )gene of the patients with phenylketonuria(PKU)in Xinjiang.
- Take the gene mutation that causes phenylketonuria or PKU. People with the disease can't break down the amino acid phenylalanine a problem that can lead to severe cognitive damage.
- Other trace elements have been observed with phenylketonuria, an inherited metabolic disorder, and kwashiorkor, a severe form of malnutrition that occurs mainly in developing nations.
