Works matching IS 00099163 AND DT 1976 AND VI 9 AND IP 3
Results: 22
X-linked ichthyosis, bilateral cryptorchidism, hypogenitalism and mental retardation in two siblings.
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- Clinical Genetics, 1976, v. 9, n. 3, p. 341, doi. 10.1111/j.1399-0004.1976.tb01583.x
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- Article
Letter to the Editor.
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- Clinical Genetics, 1976, v. 9, n. 3, p. 381, doi. 10.1111/j.1399-0004.1976.tb01593.x
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- Article
Reference interval for maternal serum alpha-fetoprotein.
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- Clinical Genetics, 1976, v. 9, n. 3, p. 374, doi. 10.1111/j.1399-0004.1976.tb01590.x
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Letters to the Editor.
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- Clinical Genetics, 1976, v. 9, n. 3, p. 378, doi. 10.1111/j.1399-0004.1976.tb01591.x
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- Article
Psychological responses to genetic counseling for Down's syndrome.
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- Clinical Genetics, 1976, v. 9, n. 3, p. 257, doi. 10.1111/j.1399-0004.1976.tb01573.x
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Letter to the Editor.
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- Clinical Genetics, 1976, v. 9, n. 3, p. 380, doi. 10.1111/j.1399-0004.1976.tb01592.x
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- Article
The position of the external ear in Turner's syndrome.
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- Clinical Genetics, 1976, v. 9, n. 3, p. 333, doi. 10.1111/j.1399-0004.1976.tb01582.x
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- Article
Familial spastic paraplegia with distal muscle wasting in the Old Order Amish; atypical Troyer syndrome or 'new' syndrome.
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- Clinical Genetics, 1976, v. 9, n. 3, p. 315, doi. 10.1111/j.1399-0004.1976.tb01580.x
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- Article
Hypospadias in successive generations - possible dominant gene inheritance.
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- Clinical Genetics, 1976, v. 9, n. 3, p. 285, doi. 10.1111/j.1399-0004.1976.tb01576.x
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A new chromosome deletion syndrome. Report of a patient with a 46, XY,8p- chromosome constitution.
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- Clinical Genetics, 1976, v. 9, n. 3, p. 289, doi. 10.1111/j.1399-0004.1976.tb01577.x
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Announcement.
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- Clinical Genetics, 1976, v. 9, n. 3, p. 383, doi. 10.1111/j.1399-0004.1976.tb01594.x
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- Article
Four cases of omphalocele in two generations of the same family.
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- Clinical Genetics, 1976, v. 9, n. 3, p. 354, doi. 10.1111/j.1399-0004.1976.tb01586.x
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- Article
45, XO/46, XYq dic mosaicism in a patient with ambiguous genitalia.
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- Clinical Genetics, 1976, v. 9, n. 3, p. 365, doi. 10.1111/j.1399-0004.1976.tb01588.x
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Recurrence risks in a consecutive series of congenitally malformed children dying in the perinatal period.
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- Clinical Genetics, 1976, v. 9, n. 3, p. 307, doi. 10.1111/j.1399-0004.1976.tb01579.x
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- Article
Ectrodactyly, ectodermal dysplasia and cleft palate (EEC syndrome):Report of a family and review of the literature.
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- Clinical Genetics, 1976, v. 9, n. 3, p. 347, doi. 10.1111/j.1399-0004.1976.tb01585.x
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- Article
Cardio-cutaneous syndrome (the 'LEOPARD' syndrome). Review of the literature and a new family.
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- Clinical Genetics, 1976, v. 9, n. 3, p. 266, doi. 10.1111/j.1399-0004.1976.tb01574.x
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A genetic study of facial clefting in Northern England.
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- Clinical Genetics, 1976, v. 9, n. 3, p. 277, doi. 10.1111/j.1399-0004.1976.tb01575.x
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- Article
The X chromosome in Duchenne's muscular dystrophy.
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- Clinical Genetics, 1976, v. 9, n. 3, p. 371, doi. 10.1111/j.1399-0004.1976.tb01589.x
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- Article
Re-evaluation of the effect of spray adhesives on human chromosomes.
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- Clinical Genetics, 1976, v. 9, n. 3, p. 302, doi. 10.1111/j.1399-0004.1976.tb01578.x
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- Article
Autosomal recessive syndrome of pseudogliomatous blindness, osteoporosis and mild mental retardation.
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- Clinical Genetics, 1976, v. 9, n. 3, p. 324, doi. 10.1111/j.1399-0004.1976.tb01581.x
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- Article
Trisomy 21 in mother and daughter.
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- Clinical Genetics, 1976, v. 9, n. 3, p. 346, doi. 10.1111/j.1399-0004.1976.tb01584.x
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Further evidence for the existence of genetically determined metabolic differences between Lp(a+) and Lp(a-) individuals.
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- Clinical Genetics, 1976, v. 9, n. 3, p. 357, doi. 10.1111/j.1399-0004.1976.tb01587.x
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- Article