Resultats de la cerca - Romain, D R

Delineation of trisomy 9 syndrome. per Romain, D R, Sullivan, J

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A rare heteromorphism of chromosome 20 and reproductive loss. per Romain, D R, Whyte, S, Callen, D F, Eyre, H J

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Two pericentric inversions, inv(2)(p11q13) and inv(5)(p13q13), in a patient referred for psychiatric problems per Romain, D R, Chapman, C J, Columbano-Green, L, Smythe, R H, Gebbie, O

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Trisomy 18 with karyotype 47,XX,-18,+i psu dic(18p). per Romain, D R, Dagger, P, Columbano-Green, L M, Smythe, R H, Parfitt, R G

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Partial monosomy for chromosome 22 in a patient with del(22)(pter----q13.1::q13.33----qter). per Romain, D R, Goldsmith, J, Cairney, H, Columbano-Green, L M, Smythe, R H, Parfitt, R G

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Cd branding studies in a homologous Robertsonian 13;13 translocation. per Romain, D R, Columbano-Green, L, Sullivan, J, Smythe, R H, Gebbie, O, Parfitt, R, Chapman, C

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Partial monosomy 12p13.1----13.3. per Romain, D R, Goldsmith, J, Columbano-Green, L M, Chapman, C J, Smythe, R H, Parfitt, R G

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Partial trisomy 14q24 leads to qter. per Romain, D R, Columbano-Green, L M, Smythe, R H, Parfitt, R G, Gebbie, O, Chapman, C J, Wall, M

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Late replication studies and esterase D levels in a case of unbalanced X;autosome translocation, 46,X,t(X;13)(q27;q12). per Romain, D R, Columbano-Green, L M, Parfitt, R G, Smythe, R H, MacKenzie, N G, Chapman, C J

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Familial distal trisomy 8(q24.13----qter). per Romain, D R, Bloxham, R A, Columbano-Green, L M, Chapman, C J, Parfitt, R G, Smythe, R H, Cairney, H

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Two cases of ring chromosome 11. per Romain, D R, Gebbie, O B, Parfitt, R G, Columbano-Green, L M, Smythe, R H, Chapman, C J, Kerr, A

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Partial trisomy for 2q in a patient with dir dup(2) (q33.1q35). per Romain, D R, Mackenzie, N G, Moss, D, Columbano-Green, L M, Smythe, R H, Parfitt, R G, Dixon, J W

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Three cases of partial trisomy 7q owing to rare structural rearrangements of chromosome 7. per Romain, D R, Cairney, H, Stewart, D, Columbano-Green, L M, Garry, M, Parslow, M I, Parfitt, R, Smythe, R H, Chapman, C J

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Mosaicism with a normal cell line and an autosomal structural rearrangement. per Gardner, R J, Dockery, H E, Fitzgerald, P H, Parfitt, R G, Romain, D R, Scobie, N, Shaw, R L, Tumewu, P, Watt, A J

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