-
1
-
-
0009650560
-
A phenotypic female with 49 chromosomes, presumably XXXXX. A case report
-
Kesaree N, Woolley PV Jr. A phenotypic female with 49 chromosomes, presumably XXXXX. A case report. J Pediatr. 1963;63:1099-1103.
-
(1963)
J Pediatr
, vol.63
, pp. 1099-1103
-
-
Kesaree, N.1
Woolley Jr., P.V.2
-
2
-
-
0032813598
-
Pentasomy X and hyper IgE syndrome: Co-existence of two distinct genetic disorders
-
DOI 10.1007/s004310051187
-
Broeck A, Gfatter R, Braun F, Fritz B. Pentasomy X and hyper IgE syndrome: co-existence of two distinct genetic disorders. Eur J Pediatr. 1999;158:723-6. (Pubitemid 29390110)
-
(1999)
European Journal of Pediatrics
, vol.158
, Issue.9
, pp. 723-726
-
-
Boeck, A.1
Gfatter, R.2
Braun, F.3
Fritz, B.4
-
4
-
-
0018606917
-
X pentasomy: A case and review
-
Archidiacono N, Rocchi M, Valente M, Filippi G. X pentasomy: a case and review. Hum Genet. 1979;52: 69-77. (Pubitemid 10194800)
-
(1979)
Human Genetics
, vol.52
, Issue.1
, pp. 69-77
-
-
Archidiacono, N.1
Rocchi, M.2
Valente, M.3
Filippi, G.4
-
5
-
-
0014040062
-
Premature menopause in XO/XX/XXX/XXXXX mosaicism
-
Gordon DL, Paulsen CA. Premature menopause in XO/XX/XXX/XXXXX mosaicism. Am J Obstet Gynecol. 1967;97:85-90.
-
(1967)
Am J Obstet Gynecol
, vol.97
, pp. 85-90
-
-
Gordon, D.L.1
Paulsen, C.A.2
-
6
-
-
0018643555
-
Pentasomy X with multiple dislocations
-
Dryer RF, Patil SR, Zellweger HU, Simpson JM, Hanson JW, Aschenbrenner C, et al. Pentasomy X with multiple dislocations. Am J Med Genet. 1979;4:313-21. (Pubitemid 10132299)
-
(1979)
American Journal of Medical Genetics
, vol.4
, Issue.4
, pp. 313-321
-
-
Dryer, R.F.1
Patil, S.R.2
Zellweger, H.U.3
-
7
-
-
0027209633
-
On the parental origin of the X's in a prenatally diagnosed 49,XXXXX syndrome
-
Martini G, Carillo G, Catizone F, Notarangelo A, Mingarelli R, Dallapiccola B. On the parental origin of the X's in a prenatally diagnosed 49,XXXXX syndrome. Prenat Diag. 1993;8:763-6. (Pubitemid 23265367)
-
(1993)
Prenatal Diagnosis
, vol.13
, Issue.8
, pp. 763-766
-
-
Martini, G.1
Carillo, G.2
Catizone, F.3
Notarangelo, A.4
Mingarelli, R.5
Dallapiccola, B.6
-
8
-
-
4444378285
-
A case of 49,XXXXX in which the extra X chromosomes were maternal in origin
-
DOI 10.1136/jcp.2004.017475
-
Cho YG, Kim DS, Lee HS, Cho SC, Choi SI. A case of 49,XXXXX in which the extra X chromosomes were maternal in origin. J Clin Pathol. 2004;57:1004-6. (Pubitemid 39208261)
-
(2004)
Journal of Clinical Pathology
, vol.57
, Issue.9
, pp. 1004-1006
-
-
Cho, Y.G.1
Kim, D.S.2
Lee, H.S.3
Cho, S.C.4
Choi, S.I.5
-
9
-
-
0018713582
-
The 49 XXXXX syndrome. Report of a case with 48 XXXX/49XXXXX mosaicism
-
Silengo MC, Davi GF, Franceschini P. The 49 XXXXX syndrome. Report of a case with 48 XXXX/49XXXXX mosaicism. Acta Pediatr Scand. 1979;68:769-71.
-
(1979)
Acta Pediatr Scand
, vol.68
, pp. 769-771
-
-
Silengo, M.C.1
Davi, G.F.2
Franceschini, P.3
-
10
-
-
0025912632
-
Penta X syndrome: A case report with review of the literature
-
Kassai R, Hamada I, Furuta H, Cho K, Abe K, Deng HX, et al. Penta X syndrome: a case report with review of the literature. Am J Med Genet. 1991;40:51-6.
-
(1991)
Am J Med Genet
, vol.40
, pp. 51-56
-
-
Kassai, R.1
Hamada, I.2
Furuta, H.3
Cho, K.4
Abe, K.5
Deng, H.X.6
|