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Items: 19

1.

A complex chromosomal rearrangement with a translocation 4;10;14 in a fertile male carrier: ascertainment through an offspring with partial trisomy 14q13-->q24.1 and partial monosomy 4q27-->q28 [corrected].

Grasshoff U, Singer S, Liehr T, Starke H, Fode B, Schöning M, Dufke A.

Cytogenet Genome Res. 2003;103(1-2):17-23. Erratum in: Cytogenet Genome Res. 2004;105(1):160.

PMID:
15004458
2.

Trisomy 4q syndrome: presentation of a new case and review of the literature.

Lundin C, Zech L, Sjörs K, Wadelius C, Annerén G.

Ann Genet. 2002 Apr-Jun;45(2):53-7. Review.

PMID:
12119211
3.

Comparative genomic hybridization based strategy for the analysis of different chromosome imbalances detected in conventional cytogenetic diagnostics.

Tönnies H, Stumm M, Wegner RD, Chudoba I, Kalscheuer V, Neitzel H.

Cytogenet Cell Genet. 2001;93(3-4):188-94.

PMID:
11528111
4.

Partial trisomy 4q and monosomy 9p resulting from a familial translocation t(4;9)(q27;p24) in a child with choanal atresia.

Wouters CH, van Bodegom TM, Moll HA, Govaerts LC.

Ann Genet. 1999;42(3):160-5.

PMID:
10526659
5.

Clarification of subtle reciprocal rearrangements using fluorescence in situ hybridization.

Sullivan BA, Leana-Cox J, Schwartz S.

Am J Med Genet. 1993 Aug 15;47(2):223-30.

PMID:
8213910
6.

Viability thresholds for partial trisomies and monosomies. A study of 1,159 viable unbalanced reciprocal translocations.

Cohen O, Cans C, Mermet MA, Demongeot J, Jalbert P.

Hum Genet. 1994 Feb;93(2):188-94. Review.

PMID:
8112744
7.

Deletions of different segments of the long arm of chromosome 4.

Mitchell JA, Packman S, Loughman WD, Fineman RM, Zackai E, Patil SR, Emanual B, Bartley JA, Hanson JW.

Am J Med Genet. 1981;8(1):73-89.

PMID:
7246608
8.
9.

Interstitial deletion of the long arm of chromosome 4 in a patient with mental retardation and abnormal phenotype.

del Valle Torrado M, Labarta JD, Migliorini AM.

J Med Genet. 1982 Dec;19(6):477. No abstract available.

10.

[Inherited translocation t(4q minus;18q plus) with unbalanced progeny of different types (author's transl)].

Knörr-Gärtner H, Knörr K, Haas B, Vogel W, Siebers JW.

Humangenetik. 1974 Mar 28;21(4):315-21. German. No abstract available.

PMID:
4135065
12.

Genetic counseling in families with inherited balanced translocations: experience with 36 families.

Wolff G, Back E, Arleth S, Rapp-Körner U.

Clin Genet. 1989 Jun;35(6):404-16.

PMID:
2736789
13.

Synaptonemal complex analysis in a human male carrier of a 4;6 translocation: heterosynapsis without previous homosynapsis.

de Perdigo A, Gabriel-Robez O, Ratomponirina C, Rumpler Y.

Hum Genet. 1991 Jan;86(3):279-82.

PMID:
1997382
15.

De novo interstitial deletion of 4q[46,XX,del(4)(q27q28.2)] with intact blood group-MN locus, confining its locus to 4q28.2-4q31.1.

Wakui K, Nishida T, Masuda J, Itoh T, Katsumata D, Ohno T, Fukushima Y.

Jinrui Idengaku Zasshi. 1991 Jun;36(2):149-53.

PMID:
1920913
16.

Partial trisomy 4q: two cases resulting from a familial translocation t(4;18)(q27;p11).

Bonfante A, Stella M, Rossi G.

Hum Genet. 1979 Nov 1;52(1):85-90.

PMID:
527978
17.

Partial trisomy 4q: two cases with a familial translocation t(4;18)(q27;q23).

Stella M, Bonfante A, Ronconi G, Rossi G.

Hum Genet. 1979 Apr 5;47(3):245-51.

PMID:
457114
18.

Partial trisomies of chromosome 21 in man. Two new observations due to translocations 19;21 and 4;21.

Pfeiffer RA, Kessel EK, Soer KH.

Clin Genet. 1977 Mar;11(3):207-13.

PMID:
138497
19.

Reciprocal translocation, 4q-; 21p+, giving rise to Down's syndrome.

Jenkins MB, Boyd L.

J Med Genet. 1976 Aug;13(4):323-6.

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