Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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11 |
Material Type: Artigo
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A case of XXX syndrome with multiple malformationsGilgenkrantz, S ; Gilgenkrantz, J M ; Fauchier, J P ; Pierson, MAnnales de génétique, 1966-09, Vol.9 (3), p.123-126NetherlandsSem texto completo |
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12 |
Material Type: Artigo
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Holoprosencephaly by triploidy 69 XXX in a 5 month old fetusEmberger, J M ; Marty-Double, C ; Pincemin, D ; Caderas de Kerleau, JAnnales de génétique, 1976-09, Vol.19 (3), p.191-193NetherlandsSem texto completo |
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13 |
Material Type: Artigo
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De novo interstitial deletion of the long arm of chromosome 2: 46,XXX,del(2)(q14q21), associated with premature craniosynostosisLucas, J ; Faivre, J ; Le Mee, F ; Hubert, S ; Pluquailec, K ; Picard, FAnnales de génétique, 1987, Vol.30 (1), p.33-38NetherlandsSem texto completo |
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14 |
Material Type: Artigo
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45 X-46 XX-47 XXX mosaic with Turner phenotype and normal ovaries. Study of a case and review of the literatureCanlorbe, P ; Toublanc, J E ; Borniche, P ; de Grouchy, JAnnales de pediatrie, 1972-12, Vol.19 (12), p.861 [Periódico revisado por pares]FranceSem texto completo |
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15 |
Material Type: Artigo
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45,X-46,XX-47,XXX karyotype and tumor of the nervous system. 2 casesAyraud, N ; Duplay, J ; Grellier, P ; Bezon, A ; Martinon, JLa Nouvelle presse medicale, 1972-12, Vol.1 (43), p.2902FranceSem texto completo |
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16 |
Material Type: Artigo
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Fertility of 45,X-46,XX and 45,X-46,XX-47,XXX womenGiraud, F ; Hartung, M ; Brusquet, Y ; Mattei, J F ; Sebahoun, A ; Serment, H ; Stahl, A ; Bernard, RAnnales de génétique, 1970-12, Vol.13 (4), p.255-258NetherlandsSem texto completo |
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17 |
Material Type: Artigo
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A case of utero-vaginal aplasia with polycystic kidney and mosaic XX=XXXLinquette, M ; Gasnault, J P ; Dupont-Lecompte, J ; Lefebvre, JBulletin de la Federation des societes de gynecologie et dobstetrique de langue francaise, 1968-01, Vol.20 (1), p.26FranceSem texto completo |
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18 |
Material Type: Artigo
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Concomitance in one family of mongolism with mosaicism (trisomy 21) in the brother and triple-X syndrome (XXX) in the sisterKlein, D ; Tajmirova, O ; Laut, J ; McGilvray, E RArchiv der Julius Klaus-Stiftung fur Vererbungsforschung, Sozialanthropologie und Rassenhygiene, 1969, Vol.44 (3-4), p.suppl 68SwitzerlandSem texto completo |
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19 |
Material Type: Artigo
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Life expectancyHealth reports, 1999, Vol.11 (3), p.9-24(Eng); 9-24(Fre) [Periódico revisado por pares]Canada: Statistics CanadaTexto completo disponível |
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20 |
Material Type: Artigo
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Postnatal diagnosis and prognosis of 2 cases of triploidyBen Hamouda, H ; Tfifha, M ; Elghezal, H ; Tlili, Y ; Soua, H ; Saad, A ; Sfar, M TArchives de pédiatrie : organe officiel de la Société française de pédiatrie, 2010-07, Vol.17 (7), p.1078-1082 [Periódico revisado por pares]FranceTexto completo disponível |