جمله انگلیسی با "phenylketonuria" + تلفظ جملات

(1) The comparison of ABR changes at the beginning of therapy against congenital hypothyroidism and phenylketonuria and later could serve as an objective criteria for follow-up of therapeutic efficiency.

(2) To understand the prevalence of thyroid hypofunction(CH) and phenylketonuria(PKU) among newborn in Penglai in order to find and treat them in time.

(3) Samples obtained through screening programme for phenylketonuria and congenital hypothyroidism.

(4) Other trace elements have been observed with phenylketonuria

(5) The management of phenylketonuria in childhood requires a multidisciplinary approach across the hospital community interface.

(6) Objective To establish a method with high efficiency in detecting phenylalanine hydroxylase(PAH) gene mutations and hence to rapidly diagnose prenatal fetals with phenylketonuria .

(7) 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.

(8) Objective To establish a method with high efficiency in detecting phenylalanine hydroxylase(PAH) gene mutations and hence to rapidly diagnose prenatal fetals with phenylketonuria .

(9) Objective To describe the incidence of congenital hypothyroidism(CH)and phenylketonuria(PKU)in Maanshan city.

(10) To explore the morbidity of Congenital hypothyroidism(CH) and phenylketonuria(PKU) among newborn in Heze city.

جمله با "phenylketonuria"

(11) The EEG in 94 patients with phenylketonuria was analyzed. The abnormality rate of EEG was 65%

(12) 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.

(13) Conclusion:The special bone changes in phenylketonuria were important X-ray signs suggestive of phenylketonuria.

(14) This result showed that PCR-SSCP analysis could be effectively used for the direct gene diagnosis of phenylketonuria.

(15) Objective To study the method for gene diagnosis of phenylketonuria.

(16) To explore the morbidity Congenital hypothyroidism ( CH ) and phenylketonuria ( PKU ) among newborn in Heze city.

(17) Objective To explore the incidence and distribution features of neonatal phenylketonuria(PKU) and congenital hypothyroidism(CH) in Lianyungang area.

(18) Objective To report the bone X ray changes in phenylketonuria.

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