Zobrazeno 1 - 10
of 10
pro vyhledávání: '"I M Orioli"'
Publikováno v:
Orthodonticscraniofacial research. 6(2)
Determine the model of inheritance of non-syndromic cleft palate in humans.Complex segregation analysis performed in families of consecutive newborns affected with non-syndromic cleft palate.The Latin American Collaborative Study of Congenital Malfor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::01ecc606040a3c2e8eab96d25670c056
https://pubmed.ncbi.nlm.nih.gov/12809269
https://pubmed.ncbi.nlm.nih.gov/12809269
Publikováno v:
Clinical genetics. 62(6)
It has been proposed that susceptibility to clefting in South America is related to Amerindian ancestry, where clefting is present at a higher frequency than in the other admixed populations (Caucasian and African) that make up the diverse racial mix
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8992391815a367a05ac8801f483cab6f
https://pubmed.ncbi.nlm.nih.gov/12485193
https://pubmed.ncbi.nlm.nih.gov/12485193
Autor:
A R, Vieira, I M, Orioli
Publikováno v:
ASDC journal of dentistry for children. 68(4)
The confirmation of supposed genes causing susceptibility to nonsyndromic cleft lip with or without a cleft palate (CL/P) and cleft palate alone (CP) would help to understand the molecular development of the lip, the palate and the jaw, and to predic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4c919a4ffc2d2d685cbd465b6b67d222
https://pubmed.ncbi.nlm.nih.gov/11862881
https://pubmed.ncbi.nlm.nih.gov/11862881
Publikováno v:
American journal of medical genetics. 93(5)
Stenosis, atresia, or absence of part of the duodenum, jejunum, or ileum are generally considered small intestinal atresias (SIAs). SIAs occur as isolated defects, in combination with other unrelated congenital anomalies, or as part of syndromes. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ca2d9086eb65abede982e2f9739c8e45
https://pubmed.ncbi.nlm.nih.gov/10951457
https://pubmed.ncbi.nlm.nih.gov/10951457
Autor:
I M, Orioli, E E, Castilla
Publikováno v:
American journal of medical genetics. 82(3)
It was recently shown that hand postaxial polydactyly differed from foot postaxial polydactyly. The aim of this work was to test whether thumb and hallux duplication also had different clinical and epidemiological characteristics, depending on limb i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::719288a33b30be32b4d982195511caa3
https://pubmed.ncbi.nlm.nih.gov/10215544
https://pubmed.ncbi.nlm.nih.gov/10215544
Publikováno v:
American journal of medical genetics. 79(2)
The first step of all healthcare actions aimed at promoting an appropriate quality of life for infants affected by Down syndrome (DS) is to ensure their survival. This investigation was aimed at estimating the infant mortality rate of infants affecte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::18de00a145496fa0b52abe521b1516da
https://pubmed.ncbi.nlm.nih.gov/9741468
https://pubmed.ncbi.nlm.nih.gov/9741468
Autor:
J S, Lopez-Camelo, I M, Orioli
Publikováno v:
Genetic epidemiology. 13(5)
The aim of this work was to disclose risk factors associated with birth defects which were heterogeneously distributed in the different geographic regions sampled by the Latin American Collaborative Study of Congenital Malformations (ECLAMC). The mat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9eb8db5b907a4328b9f83eecc556dd52
https://pubmed.ncbi.nlm.nih.gov/8905393
https://pubmed.ncbi.nlm.nih.gov/8905393
Publikováno v:
Journal of Medical Genetics. 23:328-332
This study was undertaken to establish the prevalence rates at birth of the skeletal dysplasias that can be recognised in the perinatal period. Using the data base of the Latin-American Collaborative Study of Congenital Malformations (ECLAMC), for th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ae8a265d08d4510537e87ae80ed0010
https://doi.org/10.1136/jmg.23.4.328
https://doi.org/10.1136/jmg.23.4.328
Publikováno v:
Acta anthropogenetica. 6(1)
Parental consanguinity was investigated in a series of 16, 137 non-malformed newborn infants, ascertained in 64 hospitals, of 27 cities, in seven South-American countries. Parental consanguinity was detected in 135 (0.84%) newborns, giving a mean inb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a53a8dcc628c8626af5be143af249e02
https://pubmed.ncbi.nlm.nih.gov/7138648
https://pubmed.ncbi.nlm.nih.gov/7138648
Autor:
E E, Castilla, I M, Orioli
Publikováno v:
Progress in clinical and biological research.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::400087e2d01d2f5a776c26718da67987
https://pubmed.ncbi.nlm.nih.gov/3991664
https://pubmed.ncbi.nlm.nih.gov/3991664