SCOPUS 정보 검색 플랫폼

Human Genetics

Volumn 39, Issue 3, 1977, Pages 283-291

Women heterozygous for deficiency of the (p21 → pter) region of the X chromosome are fertile

(4) Fraccaro, M a Maraschio, Paola a Pasquali, F a Scappaticci, Susi a

a UNIVERSITY OF PAVIA (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOME; CHROMATIN; CHROMOSOME DELETION X; CHROMOSOME TRANSLOCATION 15; CHROMOSOME TRANSLOCATION X; CHROMOSOME XP; DIAGNOSIS; ETIOLOGY; FERTILITY; HETEROZYGOSITY; HISTOLOGY; MAJOR CLINICAL STUDY; PARTIAL MONOSOMY X;

ADULT; CASE REPORT; CHROMOSOMES, HUMAN, 13-15; DNA REPLICATION; FEMALE; HETEROZYGOTE; HUMAN; INFERTILITY, FEMALE; KARYOTYPING; MALE; PEDIGREE; SEX CHROMOSOME ABERRATIONS; TRANSLOCATION (GENETICS);

EID: 0017667981 PISSN: 03406717 EISSN: 14321203 Source Type: Journal
DOI: 10.1007/BF00295421 Document Type: Article

Times cited : (74)

References (16)

1
- 0017287222
- Karyotyp-Phenotyp-Korrelation bei einem 46,X,del(X)(p22)-Befund
- (1976) Hum. Genet. , vol.31 , pp. 263-270
- Bartsch-Sandhoff, M.¹ Terinde, R.² Wiegelmann, W.³ Scholz, W.⁴

2
- 0017335504
- Y to X translocation in man
- (1977) Hum. Genet. , vol.36 , pp. 129-141
- van den Berghe, H.¹ Petit, P.² Fryns, J.P.³

3
- 0015134375
- An inherited X-autosome translocation in man
- (1971) Ann. Hum. Genet. , vol.35 , pp. 171-178
- Buckton, K.E.¹ Jacobs, P.A.² Rae, L.A.³ Newton, M.S.⁴ Sanger, R.⁵

4
- 0017124172
- X-short arm deletion gonadal dysgenesis in two siblings due to unique translocation (Xp-;16p+)
- (1976) Clin. Genet. , vol.10 , pp. 202-207
- Davis, J.R.¹ Wayne, H.M.² Lightner, E.S.³ Giles, H.R.⁴ Graap, R.F.⁵

5
- 0015504012
- Stérilité et translocation familiale t(1q-;Xq+)
- (1972) C. R. Sci. Natl. , vol.274 , pp. 3324-3327
- Dutrillaux, B.¹ Couturier, J.² Rotmann, J.³ Salat, J.⁴ Lejeune, J.⁵

6
- 0016209294
- Délétion partielle du bras court d'un chromosome X
- (1974) Arch. Fr. Pediatr. , vol.31 , pp. 717-724
- Giraud, F.¹ Hartung, M.² Mattei, J.F.³ Bachelet, Y.⁴ Mattei, M.G.⁵

7
- 0015939269
- Y to X translocation in a woman with reproductive failure
- (1973) JAMA , vol.226 , pp. 544-549
- Khudr, G.¹ Benirschke, K.² Judd, H.L.³ Strauss, J.⁴

8
- 0016147877
- Familial X/X translocation: t(X;X)(p22;q13)
- (1974) Cytogenet. Cell Genet. , vol.13 , pp. 454-464
- Kim, H.J.¹ Hsu, L.Y.F.² Hirschhorn, K.³

9
- 0016409479
- Sur quatre nouveaux cas de translocation du chromosome X chez l'homme
- (1975) Humangenetik , vol.26 , pp. 35-46
- Laurent, C.¹ Biemont² Dutrillaux, B.³

10
- 84931962679
- Maraschio, P., Scappaticci, S., Ferrari, E., Fraccaro, M.: X chromosomes attached by their long arms: Replication autonomy of the short arm adjacent to the inactive centromere. Ann. Génét. (in press, 1977)

11
- 0015749775
- Unbalanced X/autosomal translocation with inactivation of the normal X chromosome
- (1973) Cytogenet. Cell Genet. , vol.12 , pp. 357-366
- Mikkelsen, M.¹ Dahl, G.²

12
- 0003867059
- Blackwell, Oxford
- (1975) Blood groups in man
- Race, R.R.¹ Sanger, R.²

13
- 75449134321
- DNA replication patterns of human chromosomes
- (1963) Cytogenetic and Genome Research , vol.2 , pp. 175-193
- Schmid, W.¹

14
- 0017257663
- Aspermia, associated with a presumably balanced X/autosomal translocation. Karyotype 46,Y,t(X;5)(q28;q11)
- (1977) Hum. Genet. , vol.31 , pp. 97-106
- Stengel-Rutkowski, S.¹ Zankl, H.² Rodewald, A.³ Scharrer, S.⁴ Chaudhuri, J.P.⁵ Zang, K.D.⁶

15
- 0017027520
- A possible active segment on the inactive human X chromosome
- (1976) Chromosoma (Berl.) , vol.59 , pp. 137-145
- Therman, E.¹ Sarto, G.E.² Distéche, C.³ Denniston, C.⁴

16
- 84931962680
- Tiepolo, L., Zuffardi, O., Rodewald, A.: Nullisomy for the distal portion of Xp in a male child with a Z/Y translocation. Hum. Genet. (in press, 1977)

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.