Zobrazeno 1 - 8
of 8
pro vyhledávání: '"R H, Heller"'
Publikováno v:
Journal of Heredity. 65:209-212
165 prenatal cytogenetic analyses are reported. The culture and Giemsa or quinacrine mustard (QM) staining processes are described. Karyotypes from both Giemsa and QM metaphases were analyzed. The main indications for amniocentesis were: 1)previous c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cb79557f22a7b438d6ab78da666bd7a
https://doi.org/10.1093/oxfordjournals.jhered.a108505
https://doi.org/10.1093/oxfordjournals.jhered.a108505
Publikováno v:
Obstetrics and gynecology. 44(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e93a5d3b38fe83cec3d624d3af26a930
https://pubmed.ncbi.nlm.nih.gov/4278969
https://pubmed.ncbi.nlm.nih.gov/4278969
Autor:
R H, Heller, L S, Palmer
Publikováno v:
Pediatrics. 62(1)
Both the detection of twins and the successful execution of a double amniocentesis pose significant technical problems in prenatal diagnosis. A case is reported in which one of twins fetuses had trisomy 21 and the other was chromosomally normal. Foll
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bedff59a914ab5fbd3d42a6607764055
https://pubmed.ncbi.nlm.nih.gov/150585
https://pubmed.ncbi.nlm.nih.gov/150585
Publikováno v:
The Johns Hopkins medical journal. 139(1)
A case of cyclophosphamide-induced azoospermia, followed three years later by the birth of a normal child to the patient's wife, is described. Genetic marker studies were carried out and strongly support identification of the patient as the true biol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3efa4b4aaa37d4b76c36f6b6bf60d10d
https://pubmed.ncbi.nlm.nih.gov/948148
https://pubmed.ncbi.nlm.nih.gov/948148
Publikováno v:
Obstetrics and gynecology. 53(2)
Of 371 consecutive patients who underwent midtrimester diagnostic amniocentesis, 8 subsequently aborted spontaneously (2.2%), and 1 had a stillbirth at 24 weeks of gestation (0.17%). In 3 of the 9 patients who suffered fetal loss, infection appears t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ad87ab8d10fb415c867de2550130cd2d
https://pubmed.ncbi.nlm.nih.gov/418974
https://pubmed.ncbi.nlm.nih.gov/418974
A clinical and cytogenetic report is made of a patient with microcephaly, peculiar facies, and retardation of physical and mental development, who possesses a karyotype containing a ring chromosome No. 6 identified by Q-staining with quinacrine musta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6647bdc6262edce1f86449873fb448ff
https://europepmc.org/articles/PMC1013038/
https://europepmc.org/articles/PMC1013038/
Publikováno v:
Obstetrics and gynecology. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e9723ac94168be190f90b4a2adaa09b5
https://pubmed.ncbi.nlm.nih.gov/14268028
https://pubmed.ncbi.nlm.nih.gov/14268028
Autor:
R H, Heller
Publikováno v:
Maryland state medical journal. 20(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0853f8e70d964ea2780a34235b04facb
https://pubmed.ncbi.nlm.nih.gov/4998152
https://pubmed.ncbi.nlm.nih.gov/4998152