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Incidence of classic PKU in Italy estimated from consanguineous marriages and from neonatal
- Pages: 339-345
- First Published: November 1983
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Fetal mortality in oral cleft families (VI): A search for early embryonic and zygotic mortality
- Pages: 346-349
- First Published: November 1983
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Facial weakness and oligosyndactyly: ? independent variable features of familial type of the Möbius syndrome
- Pages: 350-354
- First Published: November 1983
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Gonadoblastoma in a patient with an isodicentric X chromosome
- Pages: 355-358
- First Published: November 1983
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Two cases of prenatal diagnosis of a satellited Yq chromosome
- Pages: 359-364
- First Published: November 1983
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Trisomy 4p in four relatives: variability and lack of distinctive features in phenotypic expression
- Pages: 365-374
- First Published: November 1983
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Partial trisomy 16q in two boys resulting from a maternal translocation, t(15;16) (p12;q11)
- Pages: 375-379
- First Published: November 1983
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A familial X/Y translocation in a boy with ichthyosis, hypogonadism and mental retardation
- Pages: 380-383
- First Published: November 1983
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45 XO/49 XYYYY Mosaicism in a male with stigmata of Turner's syndrome
- Pages: 384-388
- First Published: November 1983
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Cystic hygroma and hydrops fetalis in a fetus with trisomy 13
- Pages: 389-391
- First Published: November 1983