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PRENATAL DIAGNOSIS OF PARTIAL MONOSOMY 13q ASSOCIATED WITH OCCIPITAL ENCEPHALOCOELE IN A FETUS
PRENATAL DIAGNOSIS OF PARTIAL MONOSOMY 13q ASSOCIATED WITH OCCIPITAL ENCEPHALOCOELE IN A FETUS
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PRENATAL DIAGNOSIS OF SUPERNUMERARY der(22)t(11;22) ASSOCIATED WITH THE DANDY-WALKER MALFORMATION IN A FETUS
PRENATAL DIAGNOSIS OF SUPERNUMERARY der(22)t(11;22) ASSOCIATED WITH THE DANDY-WALKER MALFORMATION IN A FETUS
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PRENATAL DIAGNOSIS, PATHOLOGY, AND GENETIC STUDY OF FETUS IN FETU
PRENATAL DIAGNOSIS, PATHOLOGY, AND GENETIC STUDY OF FETUS IN FETU
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PRENATAL DIAGNOSIS OF CEPHALOTHORACOPAGUS JANICEPS MONOSYMMETROS
PRENATAL DIAGNOSIS OF CEPHALOTHORACOPAGUS JANICEPS MONOSYMMETROS
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Prenatal diagnosis of partial trisomy 12 and partial trisomy 21 due to a 3:1 segregation of maternal reciprocal translocation t(12;21) (p13.3;q21)
Prenatal diagnosis of partial trisomy 12 and partial trisomy 21 due to a 3:1 segregation of maternal reciprocal translocation t(12;21) (p13.3;q21)
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Prenatal diagnosis of de novo isochromosome 13q associated with microcephaly, alobar holoprosencephaly and cebocephaly in a fetus
Prenatal diagnosis of de novo isochromosome 13q associated with microcephaly, alobar holoprosencephaly and cebocephaly in a fetus
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Prenatal diagnosis of de novo interstitial 16q deletion in a fetus associated with sonographic findings of prominent coronal sutures, a prominent frontal bone, and shortening of the
Prenatal diagnosis of de novo interstitial 16q deletion in a fetus associated with sonographic findings of prominent coronal sutures, a prominent frontal bone, and shortening of the
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Concomitant chyloperitoneum and omental cysts presenting as fetal ascites with intra-abdominal cysts on prenatal ultrasound
Concomitant chyloperitoneum and omental cysts presenting as fetal ascites with intra-abdominal cysts on prenatal ultrasound
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Partial trisomy 8q and partial monosomy 15q associated with congenital hydrocephalus, diaphragmatic hernia, uinary tract anomalies, congenital heart defect and kyphoscoliosis
Partial trisomy 8q and partial monosomy 15q associated with congenital hydrocephalus, diaphragmatic hernia, uinary tract anomalies, congenital heart defect and kyphoscoliosis
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Inconsistency of omphalocoele contents in three consecutive siblings with partial trisomy 3q and partial monosomy 11q
Inconsistency of omphalocoele contents in three consecutive siblings with partial trisomy 3q and partial monosomy 11q
220 views
Bilateral renal agenesis and fetal ascites in association with partial trisomy 13 and partial trisomy 16 due to a 3:1 segregation of maternal reciprocal translocation t(13;16)(q12.3;
Bilateral renal agenesis and fetal ascites in association with partial trisomy 13 and partial trisomy 16 due to a 3:1 segregation of maternal reciprocal translocation t(13;16)(q12.3;
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Prenatal diagnosis of a fetus with distal 10q trisomy
Prenatal diagnosis of a fetus with distal 10q trisomy
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Prenatal diagnosis of partial trisomy 3p(3p23→pter) and monosomy 7q(7q36→qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia
Prenatal diagnosis of partial trisomy 3p(3p23→pter) and monosomy 7q(7q36→qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia
216 views
Fetal DNA in maternal plasma: the prenatal detection of a paternally inherited fetal aneuploidy
Fetal DNA in maternal plasma: the prenatal detection of a paternally inherited fetal aneuploidy
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Prenatal diagnosis of inherited satellited non-acrocentric chromosomes
Prenatal diagnosis of inherited satellited non-acrocentric chromosomes
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Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18
Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18
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Prenatal diagnosis of mosaic ring chromosome 13 with anencephaly
Prenatal diagnosis of mosaic ring chromosome 13 with anencephaly
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Prenatal diagnosis and genetic analysis of type I and type II thanatophoric dysplasia
Prenatal diagnosis and genetic analysis of type I and type II thanatophoric dysplasia
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A paternally derived inverted duplication of distal 14q with a terminal 14q deletion
A paternally derived inverted duplication of distal 14q with a terminal 14q deletion
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Molecular cytogenetic analysis of de novo dup(5)(q35.2q35.3) and review of the literature of pure partial trisomy 5q
Molecular cytogenetic analysis of de novo dup(5)(q35.2q35.3) and review of the literature of pure partial trisomy 5q
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