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Items: 1 to 20 of 78

1.

Partial trisomy 4q: a case report.

Cui YX, Wang YH, Hao LJ, Hou L, Li W, Huang YF.

Chin Med J (Engl). 2006 Jul 5;119(13):1136-9. No abstract available.

PMID:
16834937
3.

Partial trisomy of long arm of chromosome 4 as a result of dir dup (4)(q27q31.3) de novo.

Hubert E, Sawicka A, Wasilewska E, Midro AT.

Genet Couns. 2006;17(2):211-8.

PMID:
16970040
4.

Corpus callosum agenesis in trisomy 8p11.23 and monosomy 4q34 because of maternal translocation.

Işik U, Başaran S, Dehgan T, Apak M.

Pediatr Neurol. 2008 Jul;39(1):55-7. doi: 10.1016/j.pediatrneurol.2008.03.012.

PMID:
18555175
5.
6.

Blepharophimosis and mental retardation (BMR) phenotypes caused by chromosomal rearrangements: description in a boy with partial trisomy 10q and monosomy 4q and review of the literature.

Bartholdi D, Toelle SP, Steiner B, Boltshauser E, Schinzel A, Riegel M.

Eur J Med Genet. 2008 Mar-Apr;51(2):113-23. doi: 10.1016/j.ejmg.2007.12.005. Epub 2008 Jan 4.

PMID:
18262484
7.

Partial trisomy and partial monosomy resulting from a reciprocal segregating in a large family.

Velagaleti GV, Hawkins JC, Panova NI, Lockhart LH.

Indian J Pediatr. 2008 Sep;75(9):956-60. doi: 10.1007/s12098-008-0093-7.

PMID:
18568304
8.

Partial trisomy 4q and preaxial limb defects.

Lurie IW.

Am J Med Genet A. 2005 Oct 15;138A(3):304-5. No abstract available.

PMID:
16158438
9.

Cytogenetic and array CGH characterization of an intrachromosomal complex rearrangement of 4q in a patient with a 4q-phenotype.

Sensi A, Prontera P, Buldrini B, Palma S, Aiello V, Gruppioni R, Calzolari E, Volinia S, Martini A.

Am J Med Genet A. 2008 Jan 1;146A(1):110-5.

PMID:
18074369
10.

Phenotypic and cytogenetic spectrum of 9p trisomy.

Temtamy SA, Kamel AK, Ismail S, Helmy NA, Aglan MS, El Gammal M, El Ruby M, Mohamed AM.

Genet Couns. 2007;18(1):29-48.

PMID:
17515299
11.

Partial trisomy 9q due to maternal 9q 17q translocation.

Nampoothiri S, Lakshman LR, Anilkumar A, Thampi MV.

Indian Pediatr. 2008 Jul;45(7):595-8.

12.

Partial trisomy 4(q31qter) due to maternal 4;5 balanced translocation in a neonate.

Senses DA, Silan F, Uzun H, Alagöz D, Zafer C, Kocabay K, Karaüzüm SB, Cetin Z.

Genet Couns. 2007;18(2):163-70.

PMID:
17710868
13.

Trisomies 4 and 10 in acute myeloid leukemia: report of a new case.

Abe S, Kameoka J, Fujiwara M, Harigae H, Sasaki O, Miyamura K.

Cancer Genet Cytogenet. 2008 Aug;185(1):55-6. doi: 10.1016/j.cancergencyto.2008.04.013. No abstract available.

PMID:
18656696
14.

Prenatal diagnosis of a partial 6q trisomy: a case report.

Valerio D, Di Domenico A, Felicetti M, La Boccetta A, Ferrara C, Antonio N, Borrelli AL.

Prenat Diagn. 2006 Oct;26(10):917-9.

PMID:
16845680
15.

[A case of familial trisomy 19-20].

Guzzetta F, Righi L.

Folia Hered Pathol (Milano). 1967 Apr;16(2):63-73. Italian. No abstract available.

PMID:
5605135
16.

Partial 5p monosomy or trisomy in 11 patients from a family with a t(5;15)(p13.3;p12) translocation.

de Carvalho AF, da Silva Bellucco FT, Kulikowski LD, Toralles MB, Melaragno MI.

Hum Genet. 2008 Nov;124(4):387-92. doi: 10.1007/s00439-008-0557-x. Epub 2008 Sep 7.

PMID:
18777129
17.

Severe upper airway stenosis in a boy with partial monosomy 16p13.3pter and partial trisomy 16q22qter.

Yamada K, Uchiyama A, Arai M, Kubodera K, Yamamoto Y, Orii KO, Nagasawa H, Masuno M, Kohno Y.

Congenit Anom (Kyoto). 2009 Jun;49(2):85-8. doi: 10.1111/j.1741-4520.2009.00228.x.

PMID:
19489960
18.

Pure segmental trisomy 1q42-qter in a boy with a severe phenotype.

Percesepe A, Lugli L, Pierluigi M, Cavani S, Malacarne M, Roversi MF, Ferrari F, Forabosco A.

Am J Med Genet A. 2007 Oct 1;143A(19):2339-42. No abstract available.

PMID:
17702013
19.

Partial monosomy Xq(Xq23 --> qter) and trisomy 4p(4p15.33 --> pter) in a woman with intractable focal epilepsy, borderline intellectual functioning, and dysmorphic features.

Bartocci A, Striano P, Mancardi MM, Fichera M, Castiglia L, Galesi O, Michelucci R, Elia M.

Brain Dev. 2008 Jun;30(6):425-9. doi: 10.1016/j.braindev.2007.11.004. Epub 2007 Dec 31.

PMID:
18166284
20.

Mosaicism for terminal deletion of 4q.

Utine GE, Aktas D.

Genet Couns. 2006;17(2):205-9.

PMID:
16970039

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