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1
Abstracts of the XXX Congress of the Francophone Group of Hepatology, Gastroenterology and Pediatric Nutrition, 14-16 May 2009. Rennes, France
Abstracts of the XXX Congress of the Francophone Group of Hepatology, Gastroenterology and Pediatric Nutrition, 14-16 May 2009. Rennes, France
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Conference Proceeding 		Add to My Research

Abstracts of the XXX Congress of the Francophone Group of Hepatology, Gastroenterology and Pediatric Nutrition, 14-16 May 2009. Rennes, France

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2009, Vol.16 Spec No, p.6 [Peer Reviewed Journal]

ISSN: 0929-693X ;EISSN: 1769-664X ;PMID: 20333803

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2
MATTRESS INSERT XXX
MATTRESS INSERT XXX
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Patent 		Add to My Research

MATTRESS INSERT XXX

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3
Medicopsychosocial syndrome of polygonosomies (XXX, XXY, XYY, syndromes etc...)
Medicopsychosocial syndrome of polygonosomies (XXX, XXY, XYY, syndromes etc...)
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Article 		Add to My Research

Medicopsychosocial syndrome of polygonosomies (XXX, XXY, XYY, syndromes etc...)

Encéphale, 1976, Vol.2 (4), p.305-315 [Peer Reviewed Journal]

ISSN: 0013-7006 ;PMID: 1001241

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4
Microcapsules (XXX) comprising plant extracts and process for their preparation
Microcapsules (XXX) comprising plant extracts and process for their preparation
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Patent 		Add to My Research

Microcapsules (XXX) comprising plant extracts and process for their preparation

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5
The variability in the decision of termination of pregnancy for sex chromosome anomalies in France
The variability in the decision of termination of pregnancy for sex chromosome anomalies in France
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Thesises (postgraduate) 		Add to My Research

The variability in the decision of termination of pregnancy for sex chromosome anomalies in France

info:eu-repo/semantics/OpenAccess

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6
XXX congress of hygiene
XXX congress of hygiene
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Article 		Add to My Research

XXX congress of hygiene

La Presse medicale, 1951-01, Vol.59 (1), p.5

ISSN: 0032-7867 ;PMID: 14808063

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7
Holoprosencephaly by triploidy 69 XXX in a 5 month old fetus
Holoprosencephaly by triploidy 69 XXX in a 5 month old fetus
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Article 		Add to My Research

Holoprosencephaly by triploidy 69 XXX in a 5 month old fetus

Annales de génétique, 1976-09, Vol.19 (3), p.191

ISSN: 0003-3995 ;PMID: 1086627

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8
De novo interstitial deletion of the long arm of chromosome 2: 46,XXX,del(2)(q14q21), associated with premature craniosynostosis
De novo interstitial deletion of the long arm of chromosome 2: 46,XXX,del(2)(q14q21), associated with premature craniosynostosis
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Article 		Add to My Research

De novo interstitial deletion of the long arm of chromosome 2: 46,XXX,del(2)(q14q21), associated with premature craniosynostosis

Annales de génétique, 1987, Vol.30 (1), p.33

ISSN: 0003-3995 ;PMID: 3498427

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9
XXX syndrome. Apropos of a case
XXX syndrome. Apropos of a case
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Article 		Add to My Research

XXX syndrome. Apropos of a case

Annales médico psychologiques, 1970-05, Vol.128 (5), p.765-771 [Peer Reviewed Journal]

ISSN: 0003-4487 ;EISSN: 1769-6631 ;PMID: 5452654

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10
Primary amenorrhea due to XXX gonosomic anomaly
Primary amenorrhea due to XXX gonosomic anomaly
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Article 		Add to My Research

Primary amenorrhea due to XXX gonosomic anomaly

Bulletin de la Federation des societes de gynecologie et dobstetrique de langue francaise, 1966-06, Vol.18 (3), p.320

ISSN: 0046-3515 ;PMID: 5962906

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11
Ocular manifestations in an XXX syndrome
Ocular manifestations in an XXX syndrome
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Ocular manifestations in an XXX syndrome

Bulletin des societes d'ophtalmologie de France, 1966-09, Vol.66 (9), p.790

ISSN: 0081-1270 ;PMID: 5976431

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12
XO-XX-XXX mosaic in two monozygotic girl twins: clinical and biological similarities and differences
XO-XX-XXX mosaic in two monozygotic girl twins: clinical and biological similarities and differences
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Article 		Add to My Research

XO-XX-XXX mosaic in two monozygotic girl twins: clinical and biological similarities and differences

Annales d'endocrinologie, 1970-11, Vol.31 (6), p.1143 [Peer Reviewed Journal]

ISSN: 0003-4266 ;PMID: 5509947

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13
Concomitance in one family of mongolism with mosaicism (trisomy 21) in the brother and triple-X syndrome (XXX) in the sister
Concomitance in one family of mongolism with mosaicism (trisomy 21) in the brother and triple-X syndrome (XXX) in the sister
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Article 		Add to My Research

Concomitance in one family of mongolism with mosaicism (trisomy 21) in the brother and triple-X syndrome (XXX) in the sister

Archiv der Julius Klaus-Stiftung fur Vererbungsforschung, Sozialanthropologie und Rassenhygiene, 1969, Vol.44 (3-4), p.suppl 68

ISSN: 0003-8881 ;PMID: 4255042

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14
47 XXX karyotype in a phenotypically normal 22-year-old girl
47 XXX karyotype in a phenotypically normal 22-year-old girl
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Article 		Add to My Research

47 XXX karyotype in a phenotypically normal 22-year-old girl

Annales d'endocrinologie, 1967-01, Vol.28 (1), p.146 [Peer Reviewed Journal]

ISSN: 0003-4266 ;PMID: 6060421

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15
Proceedings: Turner phenotype with menses, leucocytes 45,X and ovarian fibroblasts 45,X-47,XXX (author's transl)
Proceedings: Turner phenotype with menses, leucocytes 45,X and ovarian fibroblasts 45,X-47,XXX (author's transl)
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Article 		Add to My Research

Proceedings: Turner phenotype with menses, leucocytes 45,X and ovarian fibroblasts 45,X-47,XXX (author's transl)

Annales d'endocrinologie, 1975-11, Vol.36 (6), p.357 [Peer Reviewed Journal]

ISSN: 0003-4266 ;PMID: 1217882

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16
Triploid (69, XXX) child having lived for 9 days
Triploid (69, XXX) child having lived for 9 days
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Article 		Add to My Research

Triploid (69, XXX) child having lived for 9 days

Annales de génétique, 1974-12, Vol.17 (4), p.283

ISSN: 0003-3995 ;PMID: 4548826

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17
45 X-47 XXX mosaicism and atypic Turner's phenotype: initial note
45 X-47 XXX mosaicism and atypic Turner's phenotype: initial note
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Article 		Add to My Research

45 X-47 XXX mosaicism and atypic Turner's phenotype: initial note

Laval medical, 1969-03, Vol.40 (3), p.280

ISSN: 0023-9046 ;PMID: 5400498

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18
Trisomy 18 and 47,XXX syndrome in the same sibship
Trisomy 18 and 47,XXX syndrome in the same sibship
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Article 		Add to My Research

Trisomy 18 and 47,XXX syndrome in the same sibship

Annales de génétique, 1969-03, Vol.12 (1), p.59

ISSN: 0003-3995 ;PMID: 5306714

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19
A case of XXX syndrome with multiple malformations
A case of XXX syndrome with multiple malformations
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A case of XXX syndrome with multiple malformations

Annales de génétique, 1966-09, Vol.9 (3), p.123

ISSN: 0003-3995 ;PMID: 5298290

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20
GONADAL DYSGENESIS WITH TALL STATURE AND 46/XX/47/XXX KARYOTYPE
GONADAL DYSGENESIS WITH TALL STATURE AND 46/XX/47/XXX KARYOTYPE
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Article 		Add to My Research

GONADAL DYSGENESIS WITH TALL STATURE AND 46/XX/47/XXX KARYOTYPE

Annales d'endocrinologie, 1964-07, Vol.25, p.454 [Peer Reviewed Journal]

ISSN: 0003-4266 ;PMID: 14177481

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