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Items: 1 to 20 of 108

1.

[Gonadosomal dysgenesia with 49 chromosomes].

Bitan A, Schaefer P, Bach C.

Ann Pediatr (Paris). 1969 Dec 2;16(12):768-72. French. No abstract available.

PMID:
5365505
2.

[Triploidy in the child. I. Study of phenotype. An observation of triploidy with mosaicism 46, XX/69, XXY].

David M, Chambon A, Laurent C, Plauchu H, Lindner D, Rouchon A, de Peretti E, Genoud J, Jeune M.

Pediatrie. 1975 Apr-May;30(3):281-98. French. No abstract available.

PMID:
1237118
3.

[The XYY status in children].

Keutel J, Dauner I.

Z Kinderheilkd. 1969;106(4):314-32. German. No abstract available.

PMID:
4980303
4.

Syndromic foramina parietalia permagna.

Chrzanowska K, Kozlowski K, Kowalska A.

Am J Med Genet. 1998 Aug 6;78(5):401-5.

PMID:
9714003
5.

Robinow or "fetal face syndrome" in a male infant with ambiguous genitalia and androgen receptor deficiency.

Schönau E, Pfeiffer RA, Schweikert HU, Böwing B, Schott G.

Eur J Pediatr. 1990 Jun;149(9):615-7.

PMID:
2373109
6.

A cytogenetic survey of 11,680 newborn infants.

Jacobs PA, Melville M, Ratcliffe S, Keay AJ, Syme J.

Ann Hum Genet. 1974 May;37(4):359-76. No abstract available.

PMID:
4277977
7.

[Ring chromosomes in mosaicism 46, XY, Cr-46, XY].

Ferrier S, Freund M, Grétillat A.

Arch Genet (Zur). 1973;46(1):1-14. French. No abstract available.

PMID:
4731928
8.

[Structural abnormalities of Y chromosome: study of 13 cases (author's transl)].

Vincent A, Gendrel D, Chaussain JL, Canlorbe P, Job JC.

Ann Pediatr (Paris). 1981 Mar;28(3):205-8. French. No abstract available.

PMID:
7224569
9.

Unique case of deletion and duplication in the long arm of the Y chromosome in an individual with ambiguous genitalia.

Thangaraj K, Subramanian S, Reddy AG, Singh L.

Am J Med Genet A. 2003 Jan 15;116A(2):205-7. No abstract available.

PMID:
12494445
10.

The clinical and cytogenetic manifestations of four cases with partial deletion of the short arm of one of the chromosomes of group B.

Zizka J, Nielsen J, Balícek P, Lichý J.

Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove Suppl. 1975;19(1):167-75. No abstract available.

PMID:
1071484
11.

Genetics of the Meckel syndrome (dysencephalia splanchnocystica).

Hsia YE, Bratu M, Herbordt A.

Pediatrics. 1971 Aug;48(2):237-47. No abstract available.

PMID:
4997860
12.

[Sirenomelia].

Znojkiewicz MH, Chagnon J.

Union Med Can. 1973 Dec;102(12):2506-10. French. No abstract available.

PMID:
4772550
13.

[Diagnosis and prevention of chromosome aberrations].

Sachs ES, van Hemel JO.

Ned Tijdschr Geneeskd. 1982 Dec 4;126(49):2236-44. Dutch. No abstract available.

PMID:
6217426
14.

[49,XXXXY syndrome in a 5-year-old boy].

Wiśniewski L, Krajewska-Walasek M, Lech H, Mospinek M.

Pediatr Pol. 1980 Jan;55(1):81-6. Polish. No abstract available.

PMID:
7189276
15.

Fetal face syndrome with acral dysostosis.

Schinzel A, Zellweger H, Grella A, Prader A.

Helv Paediatr Acta. 1974 Apr;29(1):55-60. No abstract available.

PMID:
4838165
16.

[2:12 (p25;q21) translocation classed at first as 2/X].

Pasquali F, Zuffardi O, Zamboni G, Bernardi F.

Ann Genet. 1975 Mar;18(1):64-6. French.

PMID:
50045
17.

XXXXY syndrome with mosaicism: case report.

Gardner RJ, Sands VE, Veale AM, Howarth DA, Parslow MI.

N Z Med J. 1972 Jul;76(482):22-7. No abstract available.

PMID:
4508378
18.

A 49,XXXYY male.

Salamanca-Gòmez F, Cortès R, Sànchez J, Armendares S.

Am J Med Genet. 1981;10(4):351-5. No abstract available.

PMID:
7199254
19.

New deletion syndrome: 1q43.

Juberg RC, Haney NR, Stallard R.

Am J Hum Genet. 1981 May;33(3):455-63.

20.

[Radiologic aspects of trisomy 17-18. Edward's syndrome].

Lurà A, Pistocchi GF, Dallapiccola B, Rovere V, Osti L.

Nunt Radiol. 1967;33:Suppl:163-87. Italian. No abstract available.

PMID:
5617435

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