Works matching IS 00099163 AND DT 1993 AND VI 44 AND IP 2
Results: 14
Infertility in carriers of two bisatellited marker chromosomes.
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- Clinical Genetics, 1993, v. 44, n. 2, p. 71, doi. 10.1111/j.1399-0004.1993.tb03849.x
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- Article
Effect of the fragile X anomaly on body proportions estimated by pedigree analysis.
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- Clinical Genetics, 1993, v. 44, n. 2, p. 82, doi. 10.1111/j.1399-0004.1993.tb03852.x
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Announcements.
- Published in:
- Clinical Genetics, 1993, v. 44, n. 2, p. 112, doi. 10.1111/j.1399-0004.1993.tb03860.x
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- Article
Parental origin of the supernumerary chromosome in trisomy 18.
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- Clinical Genetics, 1993, v. 44, n. 2, p. 57, doi. 10.1111/j.1399-0004.1993.tb03847.x
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- Article
Slipped capital femoral epiphysis associated with Rubinstein-Taybi syndrome.
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- Clinical Genetics, 1993, v. 44, n. 2, p. 79, doi. 10.1111/j.1399-0004.1993.tb03851.x
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- Article
46XY/47XYY mosaicism and fragile X.
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- Clinical Genetics, 1993, v. 44, n. 2, p. 109, doi. 10.1111/j.1399-0004.1993.tb03858.x
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- Article
Mspl RFLP in exon 18 of the LDL receptor gene detectable by PCR.
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- Clinical Genetics, 1993, v. 44, n. 2, p. 111, doi. 10.1111/j.1399-0004.1993.tb03859.x
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- Article
Application of molecular and cytogenetic techniques to the detection of a de novo unbalanced t(11q;21q) in a patient previously diagnosed as having monosomy 21.
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- Clinical Genetics, 1993, v. 44, n. 2, p. 89, doi. 10.1111/j.1399-0004.1993.tb03853.x
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- Article
Retinitis pigmentosa: problems associated with genetic classification.
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- Clinical Genetics, 1993, v. 44, n. 2, p. 62, doi. 10.1111/j.1399-0004.1993.tb03848.x
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- Article
Frontonasal dysplasia, lipoma of the corpus callosum and tetralogy of Fallot.
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- Clinical Genetics, 1993, v. 44, n. 2, p. 95, doi. 10.1111/j.1399-0004.1993.tb03854.x
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- Article
Ridge hypoplasia and ridge dissociation: minor physical anomalies in autistic children.
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- Clinical Genetics, 1993, v. 44, n. 2, p. 107, doi. 10.1111/j.1399-0004.1993.tb03857.x
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- Article
Prenatal screening for cystic fibrosis: attitudes and responses of participants.
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- Clinical Genetics, 1993, v. 44, n. 2, p. 102, doi. 10.1111/j.1399-0004.1993.tb03856.x
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- Article
Association of Shokeir syndrome (congenital universal alopecia, epilepsy, mental subnormality and pyorrhea) and giant pigmented nevus.
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- Clinical Genetics, 1993, v. 44, n. 2, p. 76, doi. 10.1111/j.1399-0004.1993.tb03850.x
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- Article
Kaufman oculocerebrofacial syndrome: report of two new cases and further delineation.
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- Clinical Genetics, 1993, v. 44, n. 2, p. 98, doi. 10.1111/j.1399-0004.1993.tb03855.x
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- Article