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Items: 1 to 20 of 137

1.
3.

A CGH study of 27 patients with CHARGE association.

Sanlaville D, Romana SP, Lapierre JM, Amiel J, Genevieve D, Ozilou C, Le Lorch M, Brisset S, Gosset P, Baumann C, Turleau C, Lyonnet S, Vekemans M.

Clin Genet. 2002 Feb;61(2):135-8.

PMID:
11940088
4.

Absent semicircular canals in CHARGE syndrome: radiologic spectrum of findings.

Morimoto AK, Wiggins RH 3rd, Hudgins PA, Hedlund GL, Hamilton B, Mukherji SK, Telian SA, Harnsberger HR.

AJNR Am J Neuroradiol. 2006 Sep;27(8):1663-71.

5.

Balanced t(6;8)(6p8p;6q8q) and the CHARGE association.

Hurst JA, Meinecke P, Baraitser M.

J Med Genet. 1991 Jan;28(1):54-5.

6.

A patient with interstitial deletion of the short arm of chromosome 3 (pter-->p21.2::p12-->qter) and a CHARGE-like phenotype.

Wieczorek D, Bolt J, Schwechheimer K, Gillessen-Kaesbach G.

Am J Med Genet. 1997 Apr 14;69(4):413-7.

PMID:
9098493
7.

CHARGE association in a child with de Novo chromosomal aberration 46, X,der(X)t(X;2)(p22.1;q33) detected by spectral karyotyping.

Lev D, Nakar O, Bar-Am I, Zudik A, Watemberg N, Finkelstien S, Katzin N, Lerman-Sagie T.

J Med Genet. 2000 Dec;37(12):E47. No abstract available.

8.

Trisomy 18 in a patient with CHARGE association.

Lee WT, Hou JW, Yau KI, Wang TR.

J Formos Med Assoc. 1995 Jan-Feb;94(1-2):60-2.

PMID:
7613237
9.

SEMA3E mutation in a patient with CHARGE syndrome.

Lalani SR, Safiullah AM, Molinari LM, Fernbach SD, Martin DM, Belmont JW.

J Med Genet. 2004 Jul;41(7):e94. No abstract available.

10.

CHARGE syndrome: report of 47 cases and review.

Tellier AL, Cormier-Daire V, Abadie V, Amiel J, Sigaudy S, Bonnet D, de Lonlay-Debeney P, Morrisseau-Durand MP, Hubert P, Michel JL, Jan D, Dollfus H, Baumann C, Labrune P, Lacombe D, Philip N, LeMerrer M, Briard ML, Munnich A, Lyonnet S.

Am J Med Genet. 1998 Apr 13;76(5):402-9. Review.

PMID:
9556299
11.

Choanal atresia and associated anomalies: the CHARGE association.

Duncan NO 3rd, Miller RH, Catlin FI.

Int J Pediatr Otorhinolaryngol. 1988 May;15(2):129-35.

PMID:
3397231
12.

Interstitial deletion 8q11.2-q13 with congenital anomalies of CHARGE association.

Arrington CB, Cowley BC, Nightingale DR, Zhou H, Brothman AR, Viskochil DH.

Am J Med Genet A. 2005 Mar 15;133A(3):326-30.

PMID:
15672384
13.

Coloboma and other ophthalmologic anomalies in Kabuki syndrome: distinction from charge association.

Ming JE, Russell KL, Bason L, McDonald-McGinn DM, Zackai EH.

Am J Med Genet A. 2003 Dec 15;123A(3):249-52. Review.

PMID:
14608645
14.

Middle and inner ear anomalies in a patient with CHARGE association.

Derbent M, Tokel K, Saygili A, Akkuzu B, Oto S, Coşkun M, Balci S.

Genet Couns. 2003;14(3):367-8. No abstract available.

PMID:
14577685
15.

[The CHARGE association].

Finel E, Parent P, Giroux JD, de Parscau L.

Arch Pediatr. 1996 Oct;3(10):1020-5. French.

PMID:
8952799
16.

["CHARGE" association].

Barak A, Gabis L, Mogilner B, Gelman-Kohan S.

Harefuah. 1997 Feb 16;132(4):254-8, 311. Hebrew.

PMID:
9153893
17.

Temporal bone anomaly proposed as a major criteria for diagnosis of CHARGE syndrome.

Amiel J, Attieé-Bitach T, Marianowski R, Cormier-Daire V, Abadie V, Bonnet D, Gonzales M, Chemouny S, Brunelle F, Munnich A, Manach Y, Lyonnet S.

Am J Med Genet. 2001 Mar 1;99(2):124-7.

PMID:
11241470
18.

[Molecular diagnosis of CHARGE syndrom].

Pedersen AM, Skovby F.

Ugeskr Laeger. 2007 Jan 29;169(5):402-6. Review. Danish.

PMID:
17280632
19.

[Choanal atresia and CHARGE syndrome].

Dalphin ML, Noir A, Menget A.

Pediatrie. 1993;48(7-8):537-42. Review. French.

PMID:
8165113
20.

CHARGE syndrome.

Blake KD, Prasad C.

Orphanet J Rare Dis. 2006 Sep 7;1:34. Review.

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