Zobrazeno 1 - 10
of 113
pro vyhledávání: '"L, Buentello"'
Publikováno v:
Clinical Genetics. 4:291-296
Two male sibs (46, XY) with normal penis and scrotum as well as bilateral cryptorchidism are reported. Intraabdominal uterus and Fallopian tubes were found. The pathogenesis and the possible inheritance of this developmental defect are discussed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e9a6db0c15665126fbc0480e511dc34
https://doi.org/10.1111/j.1399-0004.1973.tb01160.x
https://doi.org/10.1111/j.1399-0004.1973.tb01160.x
Publikováno v:
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 286:267-273
The cellular cycle (cc) span was measured by using differential sister-chromatid staining (DSCS) and applying the following methods: cellular cycle time (cct) according to the graphic method of Dutrillaux and Fosse (G-cct); the analytical equation (A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d995c42ec397932502359152ce46fbd
https://doi.org/10.1016/0027-5107(93)90191-h
https://doi.org/10.1016/0027-5107(93)90191-h
Publikováno v:
Scopus-Elsevier
Several blood groups, ABO, Rh, Ss, Fy, Jk, and red cell acid phosphatase (ACP) types were studied in a native Mixteca population that has resided in Mexico City since 1950. Gene frequencies were obtained and used to establish admixture estimates with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::528363f1e2053a66acf74c6e1467a63d
https://pubmed.ncbi.nlm.nih.gov/11533972
https://pubmed.ncbi.nlm.nih.gov/11533972
Publikováno v:
American journal of medical genetics. 99(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::00f8e9a5a9275c31a86cfb5f7bc9e646
https://pubmed.ncbi.nlm.nih.gov/11241483
https://pubmed.ncbi.nlm.nih.gov/11241483
Publikováno v:
Archives of medical research.
Molecular studies using polymerase chain reaction (PCR) and restriction enzymes, as well as intragenic STRs and newly designed primers, were performed in patients with Duchenne-Becker muscular dystrophy, sickle cell anemia, retinoblastoma, and nephro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::638ff480eaf0f7bde734cf4f6ae0a1f9
https://pubmed.ncbi.nlm.nih.gov/8845661
https://pubmed.ncbi.nlm.nih.gov/8845661
Publikováno v:
Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion. 45(2)
The frequency of heterochromatic polymorphisms on C-banded chromosomes 1, 9 and 16 in two inter-racial Mexican populations was analyzed. Secondary constriction (qh) regions were classified according to a semi-quantitative procedure which showed to be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0ac64d783101f591ff0d02c9bf94ebb9
https://pubmed.ncbi.nlm.nih.gov/8337542
https://pubmed.ncbi.nlm.nih.gov/8337542
Publikováno v:
Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion. 42(3)
The parents of 85 Down syndrome cases with regular 21 trisomy were studied cytogenetically. The lymphocyte chromosomes were stained with G-banding technique and 100 metaphases were analyzed in the father, the mother and the index case. Among the moth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7838125f0941d70236ccb889a87bcc00
https://pubmed.ncbi.nlm.nih.gov/2148633
https://pubmed.ncbi.nlm.nih.gov/2148633
[Usefulness of chromosomal heteromorphisms obtained by G-banding for identification of illegitimacy]
Publikováno v:
Archivos de investigacion medica. 21(2)
The present paper investigates the use of G-bands chromosome heteromorphisms for illegitimacy testing. We studied both parents and 171 of their children in 80 families utilizing the material, in addition, to establish the procedures sensitivity. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d2e268e00149b61f3e886a382176c6f5
https://pubmed.ncbi.nlm.nih.gov/2151746
https://pubmed.ncbi.nlm.nih.gov/2151746
Publikováno v:
Cytogenetic and Genome Research. 8:177-186
We present a family with a normal chromosome complement plus a tiny centric fragment with satellites on both arms in some of the members in which the proband was a child with regular G1 trisomy plus the abnormal chromosome. The authors believe that a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c17c4f5c15c17c91bdce1e02d79b206
https://doi.org/10.1159/000130060
https://doi.org/10.1159/000130060
Publikováno v:
Journal of Medical Genetics. 8:378-380
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f5ade9c51fcbf6a61cbbc35d3223a60
https://doi.org/10.1136/jmg.8.3.378
https://doi.org/10.1136/jmg.8.3.378