Results 61 to 70 of about 47,557 (115)
Some of the next articles are maybe not open access.
Radiology, 1969
In April 1960, Patau and others described a characteristic pattern of numerous anomalies associated with a trisomy in the 13–15 group (also known as D1 trisomy) (13). Although there have been over thirty published examples of trisomy 13–15, only brief mention of the disorder has been made in the radiological literature (1).
A E, James +3 more
openaire +2 more sources
In April 1960, Patau and others described a characteristic pattern of numerous anomalies associated with a trisomy in the 13–15 group (also known as D1 trisomy) (13). Although there have been over thirty published examples of trisomy 13–15, only brief mention of the disorder has been made in the radiological literature (1).
A E, James +3 more
openaire +2 more sources
Teratology, 1990
AbstractA significant number of fetuses with trisomy 13 are spontaneously or voluntarily lost before birth; however, very few such fetuses have been systemically autopsied. In the present study, ten trisomy 13 fetuses of 130–305 mm in crown‐rump length, estimated gestational age from 108 days to 239 days, were examined following either karyotype or ...
M, Fujinaga +2 more
openaire +2 more sources
AbstractA significant number of fetuses with trisomy 13 are spontaneously or voluntarily lost before birth; however, very few such fetuses have been systemically autopsied. In the present study, ten trisomy 13 fetuses of 130–305 mm in crown‐rump length, estimated gestational age from 108 days to 239 days, were examined following either karyotype or ...
M, Fujinaga +2 more
openaire +2 more sources
NeoReviews, 2012
In this paper, we review the complex medical, ethical, and psychosocial decisions that confront maternal fetal medicine specialists, neonatologists, parents, nurses, and other providers in the management of infants diagnosed with two chromosomal conditions generally considered as lethal anomalies.
T. Allen Merritt +5 more
openaire +1 more source
In this paper, we review the complex medical, ethical, and psychosocial decisions that confront maternal fetal medicine specialists, neonatologists, parents, nurses, and other providers in the management of infants diagnosed with two chromosomal conditions generally considered as lethal anomalies.
T. Allen Merritt +5 more
openaire +1 more source
Trisomy 13/trisomy 18 mosaicism in an infant
Clinical Genetics, 1996Cytogenetic analysis of amniotic fluid cells from a 31‐week‐old fetus suffering from polyhydramnios revealed that there were two cell lines, each with either trisomy 13 or trisomy 18. We studied the origin and mechanism of formation of this unique mixoploidy by tracing chromosomal heteromorphisms as genetic markers, and showed no discordance of parent ...
K, Abe +4 more
openaire +2 more sources
Recurrences of trisomy 18 and trisomy 13 after trisomy 21
Human Genetics, 1989Between 40 years and 43 years of age, a woman had three consecutive pregnancies with different prenatally diagnosed autosomal trisomies. This is compatible with the view that the predisposition to non-disjunction is not chromosome-specific.
D R, FitzPatrick, E, Boyd
openaire +2 more sources
Trisomy 13 and myelodysplastic syndrome
Cancer Genetics and Cytogenetics, 1990The clinical and cytogenetic data of a patient with myelodysplastic syndrome-refractory anemia with excess blasts (MDS-RAEB) and trisomy 13 as the sole abnormality are presented. This appears to be only the second report of such a patient. The presence of trisomy 13 is confirmed by in situ hybridization using an alphoid repeat probe L1.26, which is ...
G C, Beverstock +4 more
openaire +2 more sources
Clinical Genetics, 1976
Clinical signs of a partial trisomy of the long arm of a chromosome 13 were present in a boy with a “de novo” translocation 13p+/13q‐.
C, Stoll +3 more
openaire +2 more sources
Clinical signs of a partial trisomy of the long arm of a chromosome 13 were present in a boy with a “de novo” translocation 13p+/13q‐.
C, Stoll +3 more
openaire +2 more sources
BJOG: An International Journal of Obstetrics & Gynaecology, 1992
ABSTRACTObjective To assess the reported association between field trisomy 13 and maternal pre‐eclampsia.Design A retrospective case‐control study.Subjects Twenty‐five women who gave birth to trisomy 13 infants in southwest England between 1971 and 1989; 38 women who gave birth to trisomy 18 infants in the same region over the same ...
J F, Tuohy, D K, James
openaire +2 more sources
ABSTRACTObjective To assess the reported association between field trisomy 13 and maternal pre‐eclampsia.Design A retrospective case‐control study.Subjects Twenty‐five women who gave birth to trisomy 13 infants in southwest England between 1971 and 1989; 38 women who gave birth to trisomy 18 infants in the same region over the same ...
J F, Tuohy, D K, James
openaire +2 more sources
European Journal of Obstetrics & Gynecology and Reproductive Biology, 1995
A 41 year old multiparous woman with an uncomplicated obstetric history was referred because of pre-eclampsia. As ultrasonic examination revealed severe IUGR and multiple congenital anomalies, trisomy 13 was suspected and confirmed by amniocentesis. This chromosomal anomaly should be suspected in cases where pre-eclampsia is associated with abnormal ...
R, Heydanus, P, Defoort, M, Dhont
openaire +2 more sources
A 41 year old multiparous woman with an uncomplicated obstetric history was referred because of pre-eclampsia. As ultrasonic examination revealed severe IUGR and multiple congenital anomalies, trisomy 13 was suspected and confirmed by amniocentesis. This chromosomal anomaly should be suspected in cases where pre-eclampsia is associated with abnormal ...
R, Heydanus, P, Defoort, M, Dhont
openaire +2 more sources
Leukemia & Lymphoma, 1992
Trisomy 13 occurring as a sole cytogenetic abnormality has recently been demonstrated to have adverse prognostic significance in acute leukemia. Trisomy 13 is seen primarily in an older male population, and has been reported in treatment-associated acute leukemia and acute leukemia evolved from myelodysplastic syndromes, as well as in de novo leukemia.
M R, Baer, C D, Bloomfield
openaire +2 more sources
Trisomy 13 occurring as a sole cytogenetic abnormality has recently been demonstrated to have adverse prognostic significance in acute leukemia. Trisomy 13 is seen primarily in an older male population, and has been reported in treatment-associated acute leukemia and acute leukemia evolved from myelodysplastic syndromes, as well as in de novo leukemia.
M R, Baer, C D, Bloomfield
openaire +2 more sources