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Items: 1 to 20 of 28

1.

Prenatal diagnosis of partial trisomy 1q and monosomy X in a fetus with a congenital lung lesion and hydrops fetalis.

Pressey TL, Wilson RD, Kasperski S, Bebbington MW, Adzick NS.

Am J Med Genet A. 2007 May 15;143A(10):1104-7.

PMID:
17431907
2.
3.

Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation.

Rio M, Molinari F, Heuertz S, Ozilou C, Gosset P, Raoul O, Cormier-Daire V, Amiel J, Lyonnet S, Le Merrer M, Turleau C, de Blois MC, Prieur M, Romana S, Vekemans M, Munnich A, Colleaux L.

J Med Genet. 2002 Apr;39(4):266-70.

4.

Identification of de novo chromosome rearrangements: five cases analyzed with differential chromosome painting.

Ida T, Harada N, Abe K, Kondoh T, Yoshinaga M, Maki T, Niikawa N.

Am J Med Genet. 2002 Mar 15;108(3):182-6.

PMID:
11891682
5.

High resolution comparative genomic hybridisation in clinical cytogenetics.

Kirchhoff M, Rose H, Lundsteen C.

J Med Genet. 2001 Nov;38(11):740-4.

6.

The common features of patients with partial trisomy of the long arm of chromosome 1.

Gfatter R, Braun F, Schnedl W.

Clin Genet. 1998 Aug;54(2):161-3. Review. No abstract available.

PMID:
9761398
7.

Chromosomal findings in 150 couples referred for genetic counselling prior to intracytoplasmic sperm injection.

Mau UA, Bäckert IT, Kaiser P, Kiesel L.

Hum Reprod. 1997 May;12(5):930-7.

PMID:
9194642
8.

Partial trisomy 1q and monosomy 18q due to a de novo t(1;18)(q25;q23).

Solé MT, Rivera H, Sánchez-Corona J, Plascencia L, Cantú JM.

Ann Genet. 1983;26(2):120-2.

PMID:
6604487
9.

G-banded chromosomes of 3,415 liveborn infants.

Xia JH, Li LY, Dai HP, Xu J, Xu FM, He XX.

Chin Med J (Engl). 1984 Dec;97(12):921-7. No abstract available.

PMID:
6443290
10.

Three children with partial trisomy 1q and partial monosomy 3p.

McCarthy GT, Fear CN, Berry AC.

J Med Genet. 1986 Oct;23(5):466-7.

11.

Partial trisomy 1q25----qter.

Tawn EJ, Roberts MB, Ghazala RG, Pyta EM.

J Med Genet. 1986 Aug;23(4):371. No abstract available.

12.

Interstitial deletion of chromosome 1 [del(1)(q25q32)] in an infant with prune belly sequence.

Scarbrough PR, Files B, Carroll AJ, Quinlan RW, Finley SC, Finley WH.

Prenat Diagn. 1988 Mar;8(3):169-74.

PMID:
3375199
13.

A case of interstitial 1q deletion [46,XY,del(q25q32.1)].

Hamano S, Fukushima Y, Yamada T, Shimizu H, Okuyama M, Ito F, Maekawa K.

Ann Genet. 1987;30(2):105-8. Review.

PMID:
3314663
14.

Karyotypes of 1142 couples with recurrent abortion.

Portnoï MF, Joye N, van den Akker J, Morlier G, Taillemite JL.

Obstet Gynecol. 1988 Jul;72(1):31-4.

PMID:
3242501
15.

Common fragile sites induced by folate deprivation, BrdU and aphidicolin: their frequency and distribution in Japanese individuals.

Kuwano A, Sugio Y, Murano I, Kajii T.

Jinrui Idengaku Zasshi. 1988 Sep;33(3):355-64. No abstract available.

PMID:
3144619
16.

Cytogenetic study of 1,633 cases.

Wang SG, Ren GQ, Xue H, Shen QY, Song LL, Yuan P.

Chin Med J (Engl). 1988 Apr;101(4):231-6. No abstract available.

PMID:
3138079
17.

Clinical variability of partial duplication 1q: a clinical report and literature review.

Rosenthal J, Abeliovich D, Carmi R.

Am J Med Genet. 1987 Aug;27(4):787-92. Review.

PMID:
3122569
18.

Congenital hyperthyroidism with reciprocal translocation t(1;17)(q25;q21).

Gregori-Romero M, López-Ginés C, Gil R, Pellín A.

Hum Genet. 1989 Sep;83(2):203.

PMID:
2777262

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