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Items: 17

1.

Evidence for the existence of the human "super female".

JACOBS PA, BAIKIE AG, BROWN WM, MACGREGOR TN, MACLEAN N, HARNDEN DG.

Lancet. 1959 Sep 26;2(7100):423-5. No abstract available.

PMID:
14406377
2.

[Double aneuploidy (trisomy X, trisomy 18) in a newborn with trisomy 18 phenotype].

Pachajoa H.

Arch Argent Pediatr. 2013 Jul-Aug;111(4):e101-4. doi: 10.1590/S0325-00752013000400019. Review. Spanish.

3.

Genotype- phenotype correlation in trisomy X: a retrospective study of a selected group of 36 patients and review of literature.

Butnariu L, Rusu C, Caba L, Pânzaru M, Braha E, Grămescu M, Popescu R, Bujoranu C, Gorduza EV.

Rev Med Chir Soc Med Nat Iasi. 2013 Jul-Sep;117(3):714-21. Review.

PMID:
24502039
4.

[Gonosomal trisomy syndrome. Five case reports and review of literature].

Schwemmle C, Jungheim M, Ptok M.

Laryngorhinootologie. 2013 Nov;92(11):725-31. doi: 10.1055/s-0033-1348249. Epub 2013 Aug 8. Review. German.

PMID:
23929211
5.

Genetic aspects of premature ovarian failure: a literature review.

Cordts EB, Christofolini DM, Dos Santos AA, Bianco B, Barbosa CP.

Arch Gynecol Obstet. 2011 Mar;283(3):635-43. doi: 10.1007/s00404-010-1815-4. Epub 2010 Dec 29. Review.

PMID:
21188402
6.

[XY type gonadal dysgenesis, trisomy X and variants].

Kikuchi I, Takeuchi H, Kinoshita K.

Nihon Rinsho. 2004 Feb;62(2):309-12. Review. Japanese.

PMID:
14968537
7.

Analysis of cell-free DNA in maternal blood in screening for fetal aneuploidies: updated meta-analysis.

Gil MM, Quezada MS, Revello R, Akolekar R, Nicolaides KH.

Ultrasound Obstet Gynecol. 2015 Mar;45(3):249-66. doi: 10.1002/uog.14791. Epub 2015 Feb 1. Review.

8.

[Abnormal Y chromosome and impairment of sex determination].

Shinka T, Nakahori Y.

Nihon Rinsho. 2006 Jun 28;Suppl 2:528-32. Review. Japanese. No abstract available.

PMID:
16817458
9.

Human chromosome abnormalities as related to physical and mental dysfunction.

Heller JH.

J Hered. 1969 Sep-Oct;60(5):239-48. Review. No abstract available.

PMID:
4244249
10.

Clinical impact of somatic mosaicism in cases with small supernumerary marker chromosomes.

Liehr T, Klein E, Mrasek K, Kosyakova N, Guilherme RS, Aust N, Venner C, Weise A, Hamid AB.

Cytogenet Genome Res. 2013;139(3):158-63. doi: 10.1159/000346026. Epub 2012 Dec 29. Review.

PMID:
23295254
11.

Chromosomes and abortion.

Carr DH.

Adv Hum Genet. 1971;2:201-57. Review. No abstract available.

PMID:
4950477
12.

Cytogenetics and the pathologist.

Carr DH.

Pathol Annu. 1975;10:93-144. Review. No abstract available.

PMID:
126409
13.

The use of fluorescence techniques for the recognition of mammalian chromosomes and chromosome regions.

Caspersson T, Lindsten J, Lomakka G, Moller A, Zech L.

Int Rev Exp Pathol. 1972;11:1-72. Review. No abstract available.

PMID:
4122097
14.

Medicine and the human chromosomes.

Robinson A, Puck TT.

Proc Annu Meet Am Psychopathol Assoc. 1967;56:1-14. Review. No abstract available.

PMID:
4230195
15.

Chromosomal disorders: background and neuroradiology.

Kumar AJ, Naidich TP, Stetten G, Reiss AL, Wang H, Thomas GH, Hurko O.

AJNR Am J Neuroradiol. 1992 Mar-Apr;13(2):577-93. Review. No abstract available.

PMID:
1533086
16.

[Sex differentiation and sex chromosomes].

Shinka T, Nakahori Y.

Nihon Rinsho. 2004 Feb;62(2):247-54. Review. Japanese.

PMID:
14968529
17.

An infant with double trisomy (48,XXX, + 18)

Jaruratanasirikul S, Jinorose U.

Am J Med Genet. 1994 Jan 15;49(2):207-10. Review.

PMID:
8116670

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