Works matching IS 00099163 AND DT 1990 AND VI 37 AND IP 3
Results: 16
A case of 46,XX,r(X) (p1q1) diagnosed by in situ hybridization.
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- Clinical Genetics, 1990, v. 37, n. 3, p. 216, doi. 10.1111/j.1399-0004.1990.tb03505.x
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- Article
Terminal 7q deletion as a cause of holoprosencephaly.
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- Clinical Genetics, 1990, v. 37, n. 3, p. 238, doi. 10.1111/j.1399-0004.1990.tb03511.x
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Genetic counselling in Duchenne and Becker muscular dystrophy is problematic when carrier studies give controversial results.
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- Clinical Genetics, 1990, v. 37, n. 3, p. 179, doi. 10.1111/j.1399-0004.1990.tb03500.x
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Sotos syndrome and de novo balanced autosomal translocation (t(3;6)(p21;p21)).
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- Clinical Genetics, 1990, v. 37, n. 3, p. 226, doi. 10.1111/j.1399-0004.1990.tb03507.x
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The common fragile site in band q27 of the human X chromosome is not coincident with the fragile X.
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- Clinical Genetics, 1990, v. 37, n. 3, p. 167, doi. 10.1111/j.1399-0004.1990.tb03498.x
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Three-generation transmission of Hirschsprung's disease.
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- Clinical Genetics, 1990, v. 37, n. 3, p. 235, doi. 10.1111/j.1399-0004.1990.tb03509.x
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Proximal 15q variant as possible pitfall in the cytogenetic diagnosis of Prader-Willi syndrome.
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- Clinical Genetics, 1990, v. 37, n. 3, p. 161, doi. 10.1111/j.1399-0004.1990.tb03497.x
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Apolipoprotein A-l/C-lll gene cluster polymorphism in Saudi Arabians, Filipinos and Caucasians.
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- Clinical Genetics, 1990, v. 37, n. 3, p. 194, doi. 10.1111/j.1399-0004.1990.tb03502.x
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Announcements.
- Published in:
- Clinical Genetics, 1990, v. 37, n. 3, p. 239, doi. 10.1111/j.1399-0004.1990.tb03512.x
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- Article
A child with cystic fibrosis: I. Parental knowledge about the genetic transmission of CF and about DNA-diagnostic procedures.
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- Clinical Genetics, 1990, v. 37, n. 3, p. 198, doi. 10.1111/j.1399-0004.1990.tb03503.x
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High resolution banding of an unusual reciprocal translocation in recurrent abortions.
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- Clinical Genetics, 1990, v. 37, n. 3, p. 230, doi. 10.1111/j.1399-0004.1990.tb03508.x
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A linkage study of malignant hyperthermia (MH).
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- Clinical Genetics, 1990, v. 37, n. 3, p. 221, doi. 10.1111/j.1399-0004.1990.tb03506.x
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Monosomy X found at first trimester CVS: a diagnostic and counselling dilemma.
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- Clinical Genetics, 1990, v. 37, n. 3, p. 236, doi. 10.1111/j.1399-0004.1990.tb03510.x
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A child with cystic fibrosis: II. Subsequent family planning decisions, reproduction and use of prenatal diagnosis.
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- Clinical Genetics, 1990, v. 37, n. 3, p. 207, doi. 10.1111/j.1399-0004.1990.tb03504.x
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- Article
CSF and urine biogenic amine metabolites in Rett syndrome.
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- Clinical Genetics, 1990, v. 37, n. 3, p. 173, doi. 10.1111/j.1399-0004.1990.tb03499.x
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Comparison of anatomical location of squamous cell carcinoma within the oral cavity and oropharynx with the incidence of in vitro hyperdiploidy.
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- Clinical Genetics, 1990, v. 37, n. 3, p. 188, doi. 10.1111/j.1399-0004.1990.tb03501.x
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- Article