Works matching IS 00099163 AND DT 1986 AND VI 30 AND IP 3
Results: 17
δ-aminolevulinic acid dehydrase (porphobilinogen synthase) in two families with inherited enzyme deficiency.
- Published in:
- Clinical Genetics, 1986, v. 30, n. 3, p. 191, doi. 10.1111/j.1399-0004.1986.tb00594.x
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- Article
Dermatoglyphics in Congenital Adrenal Hyperplasia (CAH).
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- Clinical Genetics, 1986, v. 30, n. 3, p. 173, doi. 10.1111/j.1399-0004.1986.tb00591.x
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- Article
Discoid lupus erythematosus-like skin lesions in a patient with autosomal recessive chronic granulomatous disease.
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- Clinical Genetics, 1986, v. 30, n. 3, p. 184, doi. 10.1111/j.1399-0004.1986.tb00593.x
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- Article
The Johanson-Blizzard syndrome: report of a new case with special reference to the dentition and review of the literature.
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- Clinical Genetics, 1986, v. 30, n. 3, p. 177, doi. 10.1111/j.1399-0004.1986.tb00592.x
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- Article
Skeletal maturation in the XY female syndrome.
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- Clinical Genetics, 1986, v. 30, n. 3, p. 199, doi. 10.1111/j.1399-0004.1986.tb00595.x
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- Article
Pepsinogen A polymorphism in gastric mucosa and urine, with special reference to patients with gastric cancer.
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- Clinical Genetics, 1986, v. 30, n. 3, p. 202, doi. 10.1111/j.1399-0004.1986.tb00596.x
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- Article
The fetal pathology of the XXXXY-syndrome.
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- Clinical Genetics, 1986, v. 30, n. 3, p. 213, doi. 10.1111/j.1399-0004.1986.tb00597.x
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- Article
Growth curves for height in Noonan syndrome.
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- Clinical Genetics, 1986, v. 30, n. 3, p. 150, doi. 10.1111/j.1399-0004.1986.tb00587.x
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- Article
Deletion of chromosome 11 (p11p13) in a patient with Beckwith-Wiedemann syndrome.
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- Clinical Genetics, 1986, v. 30, n. 3, p. 154, doi. 10.1111/j.1399-0004.1986.tb00588.x
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- Article
Chromosomal mosaicism and maternal cell contamination in chorionic villi cultures.
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- Clinical Genetics, 1986, v. 30, n. 3, p. 239, doi. 10.1111/j.1399-0004.1986.tb00602.x
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- Article
A recent survey of consanguineous marriages in Japan.
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- Clinical Genetics, 1986, v. 30, n. 3, p. 230, doi. 10.1111/j.1399-0004.1986.tb00600.x
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- Article
Frequency of rare fragile sites among mentally subnormal schoolchildren.
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- Clinical Genetics, 1986, v. 30, n. 3, p. 234, doi. 10.1111/j.1399-0004.1986.tb00601.x
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- Article
Genetic modelling in schizophrenia according to HLA typing.
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- Clinical Genetics, 1986, v. 30, n. 3, p. 157, doi. 10.1111/j.1399-0004.1986.tb00589.x
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- Article
Familial supernumerary non-satellited microchromosome.
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- Clinical Genetics, 1986, v. 30, n. 3, p. 226, doi. 10.1111/j.1399-0004.1986.tb00599.x
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- Article
Autosomal dominant onychodystrophy and anonychia with type B brachydactyly and ectrodactyly.
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- Clinical Genetics, 1986, v. 30, n. 3, p. 219, doi. 10.1111/j.1399-0004.1986.tb00598.x
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- Article
Unusual pedigree patterns in seven families with spinal muscular atrophy; further evidence for the allelic model hypothesis.
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- Clinical Genetics, 1986, v. 30, n. 3, p. 145, doi. 10.1111/j.1399-0004.1986.tb00586.x
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- Article
Increased levels of apo-transcobalamins I and II in amniotic fluid from pregnant women with previous neural tube defect offspring.
- Published in:
- Clinical Genetics, 1986, v. 30, n. 3, p. 167, doi. 10.1111/j.1399-0004.1986.tb00590.x
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- Article