Found: 9
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Campomelic Syndrome in Phenotypic Females with 46,XY Chromosomes.
- Published in:
- Clinical Pediatrics, 1981, v. 20, n. 3, p. 214, doi. 10.1177/000992288102000308
- By:
- Publication type:
- Article
Optimized Technique for Speech Noise Elimination Using Traditional Spectrum Subtraction.
- Published in:
- IUP Journal of Telecommunications, 2011, v. 3, n. 2, p. 23
- By:
- Publication type:
- Article
Prenatal diagnosis of lethal osteogenesis imperfecta (OI) by ultrasonography.
- Published in:
- 1983
- By:
- Publication type:
- journal article
Higher Body Mass Index Is Associated with Subjective Olfactory Dysfunction.
- Published in:
- Behavioural Neurology, 2015, v. 2015, p. 1, doi. 10.1155/2015/675635
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- Publication type:
- Article
Chromosome 22 microdeletion by F.I.S.H. in isolated congenital heart disease.
- Published in:
- 2006
- By:
- Publication type:
- journal article
Birth defects surveillance study.
- Published in:
- 2005
- By:
- Publication type:
- journal article
A family with translocation 1/13: index patient with history of spontaneous abortions.
- Published in:
- 1991
- By:
- Publication type:
- case study
Chorionic villus sampling for first-trimester fetal diagnosis: preliminary experience.
- Published in:
- 1987
- By:
- Publication type:
- journal article
Trisomy 18q: 46, XX,13q+,t(13;18)(q32;q11) in a newborn associated with multiple congenital anomalies due to paternal reciprocal translocation, 46, XY,-13,+der(13)/t(13;18)(q32;q11).
- Published in:
- Clinical Genetics, 1980, v. 18, n. 4, p. 233, doi. 10.1111/j.1399-0004.1980.tb00879.x
- By:
- Publication type:
- Article