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Literature DB >> 4475024

Abnormal X chromosomes in man: origin, behavior and effects.

E Therman, K Patau.

Abstract

Entities: Species

Mesh：

Year: 1974 PMID： 4475024 DOI： 10.1007/bf00281002

Source DB: PubMed Journal: Humangenetik ISSN： 0018-7348

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46 in total

1. A CASE OF PRIMARY AMENORRHEA WITH A TRANSLOCATION INVOLVING CHROMOSOMES OF GROUPS B AND C.

Authors: J D MANN; A VALDMANIS; S C CAPPS; R H PUITE
Journal: Am J Hum Genet Date: 1965-09 Impact factor: 11.025

2. Increased Q fluorescence of an inactive Xq-chromosome in man.

Authors: G E Sarto; E Therman; K Patau
Journal: Clin Genet Date: 1974 Impact factor: 4.438

Review 3. Human genetics.

Authors: V A McKusick; G A Chase
Journal: Annu Rev Genet Date: 1973 Impact factor: 16.830

4. Trisomy 13 with a 13-X translocation.

Authors: B F Crandall; R E Carrel; J Howard; W A Schroeder; H Müller
Journal: Am J Hum Genet Date: 1974-05 Impact factor: 11.025

5. [46, XXip karyotype in a woman with normal stature and gonadal dysgenesis without other congenital anomalies].

Authors: H Van den Berghe; J P Fryns; F Devos
Journal: Humangenetik Date: 1973

6. Two human X-autosome translocations identified by autoradiography and fluorescence.

Authors: M M Cohen; C C Lin; V Sybert; E J Orecchio
Journal: Am J Hum Genet Date: 1972-09 Impact factor: 11.025

7. Somatic stigmata of Turner's syndrome in a patient with 46,XXq-.

Authors: M Bocian; E Krmpotic; K Szego; I M Rosenthal
Journal: J Med Genet Date: 1971-09 Impact factor: 6.318

8. Multiple abnormalities due to possible genetic inactivation in an X-autosome translocation.

Authors: T H Thelen; D J Abrams; R O Fisch
Journal: Am J Hum Genet Date: 1971-07 Impact factor: 11.025

9. [Duplication of an X chromosome in a case of Turner's syndrome (45,X-46,XXp+)].

Authors: I Emerit; J German; L P Crippa; C Sureau
Journal: Ann Genet Date: 1970-12

10. Cytological mapping of human X-linked genes by use of somatic cell hybrids involving an X-autosome translocation (mouse-hamster-human X-linked markers).

Authors: K H Grzeschik; P W Allderdice; A Grzeschik; J M Opitz; O J Miller; M Siniscalco
Journal: Proc Natl Acad Sci U S A Date: 1972-01 Impact factor: 11.205

57 in total

1. Linkage analysis of Norrie disease with X-chromosomal ornithine aminotransferase.

Authors: J B Bateman
Journal: Trans Am Ophthalmol Soc Date: 1992

2. Necropsy findings in a fetus with a 46,XY,dic t(X;21)(p11.1;p11.1).

Authors: N M Smith; H Fernandez; H M Chambers; D F Callen
Journal: J Med Genet Date: 1992-07 Impact factor: 6.318

3. Short arm deletion of an X chromosome, 46,XXp-.

Authors: P Kaiser; B Zabel; S Hansen; E Daume
Journal: Hum Genet Date: 1976-04-15 Impact factor: 4.132

4. Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy.

Authors: H F Willard; S A Latt
Journal: Am J Hum Genet Date: 1976-05 Impact factor: 11.025

5. Center for Barr body condensation. A case of Turner's syndrome with 45,X/46,X,dic(X) (Xqter leads to p22::p22 leads to qter).

Authors: I Sillesen; K Rasmussen; O Osterballe; J Nielsen
Journal: Hum Genet Date: 1976-08-30 Impact factor: 4.132

6. BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes.

Authors: S A Latt; H F Willard; P S Gerald
Journal: Chromosoma Date: 1976-08-17 Impact factor: 4.316