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Publications by authors named "E McGilvray"

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A balanced 13-18 translocation [46,XY,t(13q-;18q+)] in the father of an infant with multiple anomalies.
E McGilvray T Kajii M Freund F Bamatter D Klein

Humangenetik

October 1971

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Partial deletion of the short arm of chromosome no. 4(4p-): clinical studies in five unrelated patients.
O J Miller W R Breg D Warburton D A Miller A DeCapoa E McGilvray

J Pediatr

November 1970

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The 13q-deletion syndrome.
P W Allderdice J G Davis O J Miller H P Klinger D Warburton E McGilvray

Am J Hum Genet

September 1969

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[Concomitance in one family of mongolism with mosaicism (trisomy 21) in the brother and triple-X syndrome (XXX) in the sister].
D Klein O Tajmirova J Laut E R McGilvray

Arch Julius Klaus Stift Vererbungsforsch Sozialanthropol Rassenhyg

November 1971

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Acute leukemia with Ph1-like chromosome in an LSD user.
L Grossbard D Rosen E McGilvray A De Capoa O Miller

JAMA

September 1968

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