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Acardius Anceps: Report of 3 Cases.
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- Journal of Obstetrics & Gynaecology Research, 1991, v. 17, n. 1, p. 49, doi. 10.1111/j.1447-0756.1991.tb00251.x
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- Article
Prenatal diagnosis of Apert syndrome with widely separated cranial sutures.
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- Prenatal Diagnosis, 2000, v. 20, n. 3, p. 254, doi. 10.1002/(SICI)1097-0223(200003)20:3<254::AID-PD775>3.0.CO;2-N
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- Publication type:
- Article
MISDIAGNOSIS OF HOMOZYGOUS ALPHA-THALASSAEMIA 1 MAY OCCUR IF POLYMERASE CHAIN REACTION ALONE IS USED IN PRENATAL DIAGNOSIS.
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- Prenatal Diagnosis, 1997, v. 17, n. 6, p. 505, doi. 10.1002/(SICI)1097-0223(199706)17:6<505::AID-PD104>3.0.CO;2-R
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- Article
Ultrasonographic scanning of placental thickness and the prenatal diagnosis of homozygous alpha-thalassaemia 1 in the second trimester.
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- 1995
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- Publication type:
- journal article
Prenatal diagnosis of 46,XX/47,XXY mosaicism: a case report.
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- 1995
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- Publication type:
- journal article
Prenatal diagnosis of X-linked hydrocephalus in a Chinese family with four successive affected pregnancies.
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- 1994
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- Publication type:
- journal article
Prenatal diagnosis of Hb H disease due to compound heterozygosity for South-East Asian deletion and Hb constant spring by polymerase chain reaction.
- Published in:
- Prenatal Diagnosis, 1993, v. 13, n. 2, p. 143, doi. 10.1002/pd.1970130210
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- Publication type:
- Article
DNA polymorphism and globin chain analysis in the prenatal diagnosis of β-thalassaemia major in Taiwan.
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- Prenatal Diagnosis, 1990, v. 10, n. 4, p. 237, doi. 10.1002/pd.1970100405
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- Publication type:
- Article
Prenatal diagnosis of chinese homozygous α-thalassaemia 1 and haemoglobin H disease by analysis of α- and φζ-globin genes in chorionic villi and amniocytes.
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- Prenatal Diagnosis, 1989, v. 9, n. 10, p. 715, doi. 10.1002/pd.1970091007
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- Publication type:
- Article
Umbilical artery flow velocity waveforms in fetuses dying with congenital anomalies.
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- BJOG: An International Journal of Obstetrics & Gynaecology, 1988, v. 95, n. 5, p. 478, doi. 10.1111/j.1471-0528.1988.tb12800.x
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- Publication type:
- Article
Massively parallel sequencing analysis of nondegraded and degraded DNA mixtures using the ForenSeq™ system in combination with EuroForMix software.
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- International Journal of Legal Medicine, 2019, v. 133, n. 1, p. 25, doi. 10.1007/s00414-018-1961-y
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- Publication type:
- Article
Fifteen non-CODIS autosomal short tandem repeat loci multiplex data from nine population groups living in Taiwan.
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- International Journal of Legal Medicine, 2012, v. 126, n. 4, p. 671, doi. 10.1007/s00414-012-0691-9
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- Article
Erratum to: Quantifying the legacy of the Chinese Neolithic on the maternal genetic heritage of Taiwan and Island Southeast Asia.
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- 2016
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- Publication type:
- Erratum
Quantifying the legacy of the Chinese Neolithic on the maternal genetic heritage of Taiwan and Island Southeast Asia.
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- Human Genetics, 2016, v. 135, n. 4, p. 363, doi. 10.1007/s00439-016-1640-3
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- Publication type:
- Article
Resolving the ancestry of Austronesian-speaking populations.
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- Human Genetics, 2016, v. 135, n. 3, p. 309, doi. 10.1007/s00439-015-1620-z
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- Publication type:
- Article
Reduced doses of hepatitis B immune globulin in the prevention of perinatal transmission of hepatitis B.
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- Journal of Medical Virology, 1987, v. 21, n. 4, p. 301, doi. 10.1002/jmv.1890210402
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- Article
Inadequacy of lmmunoglobulin M hepatitis B core antibody in detecting acute hepatitis B virus infection in infants of HBsAg carrier mothers.
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- Journal of Medical Virology, 1985, v. 16, n. 4, p. 309, doi. 10.1002/jmv.1890160402
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- Publication type:
- Article
Rapid Detection of Chinese <sup>G</sup>γ+(<sup>A</sup>γδβ)° -Thalassemia by Polymerase Chain Reaction.
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- Acta Haematologica, 1993, v. 89, n. 2, p. 80, doi. 10.1159/000204492
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- Article
Corrigendum.
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- American Journal of Hematology, 1999, v. 60, n. 2, p. 173, doi. 10.1002/(SICI)1096-8652(199902)60:2<173::AID-AJH23>3.0.CO;2-A
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- Publication type:
- Article
Molecular characterization and PCR diagnosis of Thailand deletion of α-globin gene cluster.
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- American Journal of Hematology, 1998, v. 57, n. 2, p. 124, doi. 10.1002/(SICI)1096-8652(199802)57:2<124::AID-AJH6>3.0.CO;2-Y
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- Publication type:
- Article
A novel heterozygous missense mutation 377T > C (V126A) of TGIF gene in a family segregated with holoprosencephaly and moyamoya disease.
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- Prenatal Diagnosis, 2006, v. 26, n. 3, p. 226, doi. 10.1002/pd.1385
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- Publication type:
- Article
Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3→qter) and partial trisomy 18q (18q23→qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
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- Prenatal Diagnosis, 2005, v. 25, n. 6, p. 492, doi. 10.1002/pd.1179
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- Publication type:
- Article
Cost-effectiveness analysis of triple test in second-trimester maternal serum screening for Down’s syndrome: an experience from Taiwan with decreasing birth rate but increasing population of old pregnant women.
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- Journal of Evaluation in Clinical Practice, 2008, v. 14, n. 2, p. 191, doi. 10.1111/j.1365-2753.2007.00831.x
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- Publication type:
- Article
Risk prediction for Down’s syndrome in young pregnant women using maternal serum biomarkers: determination of cut-off risk from receiver operating characteristic curve analysis.
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- Journal of Evaluation in Clinical Practice, 2007, v. 13, n. 2, p. 254, doi. 10.1111/j.1365-2753.2006.00687.x
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- Publication type:
- Article
Prenatal Diagnosis of Placental Mesenchymal Dysplasia with 46, X, Isochromosome Xq/45, X Mosaicism.
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- Genes, 2022, v. 13, n. 2, p. 245, doi. 10.3390/genes13020245
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- Article
Molecular genetic study of Pompe disease in Chinese patients in Taiwan.
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- Human Mutation, 1999, v. 13, n. 5, p. 380, doi. 10.1002/(SICI)1098-1004(1999)13:5<380::AID-HUMU6>3.0.CO;2-A
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- Publication type:
- Article
Homozygous mutation 341delG/101X of the glucose-6-phosphatase (G6PC) gene causes glycogen storage disease type Ia (von Gierke disease) in a Chinese patient.
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- Human Mutation, 1999, v. 13, n. 5, p. 414, doi. 10.1002/(SICI)1098-1004(1999)13:5<414::AID-HUMU17>3.0.CO;2-5
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- Publication type:
- Article
Study of the Cytochrome b Gene Sequence in Populations of Taiwan.
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- Journal of Forensic Sciences, 2010, v. 55, n. 1, p. 167, doi. 10.1111/j.1556-4029.2009.01195.x
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- Article
Incontinentia pigmenti in a male infant and a proposed diagnostic algorithm.
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- Clinical & Experimental Dermatology, 2022, v. 47, n. 7, p. 1366, doi. 10.1111/ced.15170
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- Article