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Items: 1 to 20 of 21

1.

An inversion inv(4)(p12-p15.3) in autistic siblings implicates the 4p GABA receptor gene cluster.

Vincent JB, Horike SI, Choufani S, Paterson AD, Roberts W, Szatmari P, Weksberg R, Fernandez B, Scherer SW.

J Med Genet. 2006 May;43(5):429-34. Epub 2006 Mar 23.

2.

Utility of multicolor fluorescent in situ hybridization in clinical cytogenetics.

Jalal SM, Law ME.

Genet Med. 1999 Jul-Aug;1(5):181-6.

PMID:
11256670
3.

Chromosomal aberrations in couples undergoing intracytoplasmic sperm injection: influence on implantation and ongoing pregnancy rates.

Scholtes MC, Behrend C, Dietzel-Dahmen J, van Hoogstraten DG, Marx K, Wohlers S, Verhoeven H, Zeilmaker GH.

Fertil Steril. 1998 Nov;70(5):933-7.

PMID:
9806579
4.

Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: a collaborative study.

Hsu LY, Yu MT, Richkind KE, Van Dyke DL, Crandall BF, Saxe DF, Khodr GS, Mennuti M, Stetten G, Miller WA, Priest JH.

Prenat Diagn. 1996 Jan;16(1):1-28.

PMID:
8821848
5.

Clinical manifestations of trisomy 4p syndrome.

Patel SV, Dagnew H, Parekh AJ, Koenig E, Conte RA, Macera MJ, Verma RS.

Eur J Pediatr. 1995 Jun;154(6):425-31. Review.

PMID:
7671938
6.

The MNSs blood groups of families with chromosome 4 rearrangements.

Cook PJ, Lindenbaum RH, Salonen R, de la Chapelle A, Daker MG, Buckton KE, Noades JE, Tippett P.

Ann Hum Genet. 1981 Feb;45(Pt 1):39-47. No abstract available.

PMID:
7316476
7.

Prenatal diagnosis in 3,000 women for chromosome, X-linked, and metabolic disorders.

Daniel A, Stewart L, Saville T, Brookwell R, Paull H, Purvis-Smith S, Lam-Po-Tang PR.

Am J Med Genet. 1982 Jan;11(1):61-75.

PMID:
7065004
8.

Interstitial deletion of the short arm of chromosome 4.

Ray M, Evans J, Rockman-Greenberg C, Wickstrom D.

J Med Genet. 1984 Jun;21(3):223-5.

9.

Balanced rearrangements of the autosomes: results of a longitudinal study of a newborn survey population.

Tierney I, Axworthy D, Smith L, Ratcliffe SG.

J Med Genet. 1984 Feb;21(1):45-51.

10.

A rare heterochromatic variant of chromosome 4.

Docherty Z, Bowser-Riley SM.

J Med Genet. 1984 Dec;21(6):470-2.

11.

Trisomy 4p in four relatives: variability and lack of distinctive features in phenotypic expression.

Reynolds JF, Shires MA, Wyandt HE, Kelly TE.

Clin Genet. 1983 Nov;24(5):365-74.

PMID:
6418421
12.

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
14.

A third case of de novo partial trisomy 4p.

Oorthuys JW, Gerssen-Schoorl KB, de Pater JM, de France HF.

J Med Genet. 1989 May;26(5):344-5. No abstract available.

15.

First report of management and outcome of pregnancies associated with hereditary orotic aciduria.

Bensen JT, Nelson LH, Pettenati MJ, Block SM, Brusilow SW, Livingstone LR, Burton BK.

Am J Med Genet. 1991 Dec 15;41(4):426-31.

PMID:
1776631
16.

[Trisomy 4p. Three new observations (author's transl)].

Giraud F, Mattei JF, Mattei MG, Ayme S, Bernard R.

Humangenetik. 1975 Nov 6;30(2):99-108. French.

PMID:
1193607
17.

Trisomy 4p due to a paternal t(4p-;16p+) translocation.

Bauknecht T, Betteken F, Vogel W.

Hum Genet. 1976 Oct 28;34(2):227-30.

PMID:
1002146
18.

Two cases of trisomy 4p with translocation t(4p-,7q+) in several members of one family.

Andrle M, Erlach A, Killian W, Rett A.

Hum Genet. 1976 Jul 27;33(2):155-60.

PMID:
939567
19.

A 13-year-old girl with Wolf's syndrome and karyotype 46,XX,del(4)(pter integral p15::p12 integral qter),9qh+. Increased risk of structural chromosome abnormalities in the progeny of mothers with 9qh+.

Nielsen J, Fischer O, Rasmussen K, Sillesen I, Bernsen A, SaldaƱa-Garcia P.

J Ment Defic Res. 1977 Jun;21(2):119-26. No abstract available.

PMID:
894706
20.

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