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Abnormal Chromosome 18 in prenatal diagnosis with holoprosencephaly

โœ Scribed by J. M. de Pater; J. M. J. C. Scheres; J. Brons


Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
27 KB
Volume
17
Category
Article
ISSN
0197-3851

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Prenatal diagnosis of a dup(3p) with hol
โœ Gillerot, Yves ;Hustin, Jean ;Koulischer, Lucien ;Viteux, Vincent ;Neri, Giovann ๐Ÿ“‚ Article ๐Ÿ“… 1987 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 217 KB ๐Ÿ‘ 2 views

The prenatal diagnosis of dup(3p) was made in a female conceptus, the father being a known carrier of a balanced translocation t(3; lO)(p21 ;q26). Interruption of pregnancy at 19 weeks showed a fetus with a holoprosencephaly field defect. Two other cases of dup(3p) have been observed in the same fam

Prenatal diagnosis of holoprosencephaly
โœ Norma J. Leonard; Darrell J. Tomkins; Nestor Demianczuk ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 120 KB ๐Ÿ‘ 2 views

Alobar holoprosencephaly (HPE) was identiยฎed by ultrasonography at 18 weeks' gestation in a fetus of a 29-year-old G2P0A1 woman. HPE has been described in association with various chromosomal anomalies. Amniocentesis was performed and a rearrangement of chromosome 18 resembling an isochromosome for