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American Journal of Medical Genetics|April 1, 1983
Duplication 8q syndrome due to familial chromosome ins(10;8)(q21;q212q22)P Bowen, P H Fitzgerald, R J Gardner, et al.American Journal of Medical Genetics|April 1, 1983
Congenital heart anomalies in the trisomy 18 syndrome, with reference to congenital polyvalvular diseaseR Matsuoka, K Misugi, A Goto, et al.American Journal of Medical Genetics|April 1, 1983
Familial agnathia-holoprosencephalyR M Pauli, J C Pettersen, S Arya, et al.American Journal of Medical Genetics|April 1, 1983
Fragile (X) X-linked mental retardation I: relationship between age and intelligence and the frequency of expression of fragil (X)(q28)A E Chudley, J Knoll, J W Gerrard, et al.American Journal of Medical Genetics|June 1, 1982
Assessment of clinical variables and counseling needs in patients with retinitis pigmentosaJ A Boughman, R J CaldwellAmerican Journal of Medical Genetics|December 1, 1982
A 15 leads to 1 translocation in a patient mosaic for presence or absence of an isodic(15p)(q11)E A Wulfsberg, R S Sparkes, I J Klisak, et al.American Journal of Medical Genetics|June 1, 1982
Studies of malformation syndromes of humans XXXIIIC: the FG syndrome - further studies on three affected individuals from the FG familyJ M Opitz, E G Kaveggia, W N Adkins, et al.American Journal of Medical Genetics|December 1, 1984
Prenatal diagnosis: the experience in families who have childrenR B Black, R FurlongAmerican Journal of Medical Genetics|August 1, 1984
The first Meckel oration: on the causes of morphological differences in a population of guinea pigsS WrightAmerican Journal of Medical Genetics|August 1, 1984
On the statistical determination of major gene mechanisms in continuous human traits: regressive modelsG E BonneyPageof 854