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PRENATAL DIAGNOSIS OF HAEMOGLOBIN BART'S DISEASE BY CORDOCENTESIS AT 12-14 WEEKS' GESTATION.
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- Prenatal Diagnosis, 1997, v. 17, n. 6, p. 501, doi. 10.1002/(SICI)1097-0223(199706)17:6<501::AID-PD89>3.0.CO;2-L
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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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FIRST-TRIMESTER SONOGRAPHY OF PHYSIOLOGICAL MIDGUT HERNIATION AND EARLY DIAGNOSIS OF OMPHALOCELE.
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- Prenatal Diagnosis, 1997, v. 17, n. 6, p. 511, doi. 10.1002/(SICI)1097-0223(199706)17:6<511::AID-PD102>3.0.CO;2-Y
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FETAL CHOROID PLEXUS CYSTS-IS A GENETIC EVALUATION INDICATED?
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- Prenatal Diagnosis, 1997, v. 17, n. 6, p. 519, doi. 10.1002/(SICI)1097-0223(199706)17:6<519::AID-PD103>3.0.CO;2-N
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FIRST-TRIMESTER URINE FREE BETA hCG, BETA CORE, AND TOTAL OESTRIOL IN PREGNANCIES AFFECTED BY DOWN'S SYNDROME: IMPLICATIONS FOR FIRST-TRIMESTER SCREENING WITH NUCHAL TRANSLUCENCY AND SERUM FREE BETA hCG.
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- Prenatal Diagnosis, 1997, v. 17, n. 6, p. 525, doi. 10.1002/(SICI)1097-0223(199706)17:6<525::AID-PD105>3.0.CO;2-I
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PRENATAL DETECTION OF Hb MUTATIONS USING TRANSCERVICAL CELLS.
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- Prenatal Diagnosis, 1997, v. 17, n. 6, p. 539, doi. 10.1002/(SICI)1097-0223(199706)17:6<539::AID-PD106>3.0.CO;2-8
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THE ROLE OF REDUCED EAR SIZE IN THE PRENATAL DETECTION OF CHROMOSOMAL ABNORMALITIES.
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- Prenatal Diagnosis, 1997, v. 17, n. 6, p. 545, doi. 10.1002/(SICI)1097-0223(199706)17:6<545::AID-PD108>3.0.CO;2-3
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BIOCHEMICAL AND MORPHOLOGICAL EXPRESSION OF EARLY PRENATAL CAPRINE β-MANNOSIDOSIS.
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- Prenatal Diagnosis, 1997, v. 17, n. 6, p. 551, doi. 10.1002/(SICI)1097-0223(199706)17:6<551::AID-PD109>3.0.CO;2-1
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STRATEGIES AND OUTCOMES OF PRENATAL DIAGNOSIS FOR OSTEOGENESIS IMPERFECTA: A REVIEW OF BIOCHEMICAL AND MOLECULAR STUDIES COMPLETED IN 129 PREGNANCIES.
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- Prenatal Diagnosis, 1997, v. 17, n. 6, p. 559, doi. 10.1002/(SICI)1097-0223(199706)17:6<559::AID-PD111>3.0.CO;2-G
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- Article
PRENATAL DIAGNOSIS OF A DELETION OF 18q IN A FETUS ASSOCIATED WITH MULTIPLE-MARKER SCREEN POSITIVE RESULTS.
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- Prenatal Diagnosis, 1997, v. 17, n. 6, p. 571, doi. 10.1002/(SICI)1097-0223(199706)17:6<571::AID-PD88>3.0.CO;2-H
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PRENATAL DIAGNOSIS OF LARYNGEAL ATRESIA IN TWO CASES OF CONGENITAL HIGH AIRWAY OBSTRUCTION SYNDROME (CHAOS).
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- Prenatal Diagnosis, 1997, v. 17, n. 6, p. 577, doi. 10.1002/(SICI)1097-0223(199706)17:6<577::AID-PD90>3.0.CO;2-M
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DIAGNOSTIC ECHOGRAPHIC FINDINGS IN CRYPTOPHTHALMOS SYNDROME (FRASER SYNDROME).
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- Prenatal Diagnosis, 1997, v. 17, n. 6, p. 582, doi. 10.1002/(SICI)1097-0223(199706)17:6<582::AID-PD107>3.0.CO;2-Y
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LETTER TO THE EDITOR. YET ANOTHER VARIATION ON THE THEME OF CHROMOSOME 18 HETERMORPHISMS?
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- Prenatal Diagnosis, 1997, v. 17, n. 6, p. 585, doi. 10.1002/(SICI)1097-0223(199706)17:6<585::AID-PD101>3.0.CO;2-C
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Letter to the Editor. Confirmation of fetal aneuploidy with primed in situ hybridization on amniotic fluid during selective fetal reduction.
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- Prenatal Diagnosis, 1997, v. 17, n. 6, p. 586, doi. 10.1002/(SICI)1097-0223(199706)17:6<586::AID-PD110>3.0.CO;2-D
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Letter to the Editor. Turner's syndrome 45,X found by coelocentesis.
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- Prenatal Diagnosis, 1997, v. 17, n. 6, p. 588, doi. 10.1002/(SICI)1097-0223(199706)17:6<588::AID-PD116>3.0.CO;2-U
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Letter to the Editor. Isochromosome 18q revisited.
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- Prenatal Diagnosis, 1997, v. 17, n. 6, p. 589, doi. 10.1002/(SICI)1097-0223(199706)17:6<589::AID-PD126>3.0.CO;2-S
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