SCOPUS 정보 검색 플랫폼

Human Genetics

Volumn 36, Issue 1, 1977, Pages 35-41

Partial trisomy 12p due to t(12;21)pat translocation

(4) Biederman, B a Bowen, P a Robertson, C a Schiff, D a

a UNIVERSITY OF ALBERTA (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 12P; CYTOLOGY; DIAGNOSIS; ETIOLOGY; HISTOLOGY; MAJOR CLINICAL STUDY; PARTIAL TRISOMY 12; PHENOTYPE;

CASE REPORT; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, 21-22 AND Y; CHROMOSOMES, HUMAN, 6-12 AND X; FEMALE; HUMAN; INFANT; INFANT, NEWBORN; PEDIGREE; PHENOTYPE; TRANSLOCATION (GENETICS); TRISOMY;

EID: 0017342392 PISSN: 03406717 EISSN: 14321203 Source Type: Journal
DOI: 10.1007/BF00390433 Document Type: Article

Times cited : (24)

References (11)

1
- 84932012858
- Alfi, O. S., Lange, M.: Trisomy 12p. A clinically recognizable syndrome. p. 189. Abstracts of the 1976 Birth Defects Conference, Vancouver, B.C.

2
- 0016715326
- Le syndrome de la trisomie 12p
- (1975) Ann. Genet. , vol.18 , pp. 89-94
- Armendares, S.¹ Salamanca, F.² Nava, S.³ Ramirez, S.⁴ Cantu, J.-M.⁵

3
- 0016765768
- Human acrocentric ring chromosomes and satellite association
- (1975) Ann. Genet. , vol.18 , pp. 193-196
- Cantu, J.-M.¹ Salmanca, F.² Sanchez, J.³ Pena, T.⁴ Pacheco, C.⁵ Armendares, S.⁶

4
- 0015592237
- Assignment of the genes for malate oxidoreductase decarboxylating to chromosome 6 and peptidase B and lactate dehydrogenase B to chromosome 12 in man
- (1973) Am. J. Hum. Genet. , vol.25 , pp. 200-207
- Chen, T.R.¹ McMorris, F.A.² Greagan, R.³ Ricciuti, F.⁴ Tischfield, J.⁵ Ruddle, F.H.⁶

5
- 0017280379
- Human nucleolar organizer chromosomes: satellite associations
- (1976) Chromosoma (Berl.) , vol.55 , pp. 81-84
- Denton, T.E.¹ Howell, W.M.² Barrett, J.V.³

6
- 0016265014
- Trisomy 12p due to familial t(12p-, 6q+) translocation
- (1974) Humangenetik , vol.24 , pp. 247-252
- Fryns, J.P.¹ Van den Berghe, H.² Van Herck, G.³ Cassiman, J.J.⁴

7
- 0016734383
- Une observation de deletion partielle du bras court du chromosome 12
- (1975) Localization du gene de la lacticodeshydrogenase B , vol.233 , pp. 275-279
- Malpuech, G.¹ Kaplan, J.C.² Réthore, M.O.³ Junien, C.⁴ Geneix, A.⁵

8
- 84932012859
- Paris Conference (1971), Supplement (1975): Standardization in Human Cytogenetics. Birth Defects: Orig. Art. Ser. XI, 9, 1975. New York: The National Foundation

9
- 0016750820
- Augmentation de l'activité de la LDH-B chez un garçon trisomique 12p par malségregation d'une translocation maternelle t(12;14)(q12;p11)
- (1975) Ann. Genet. , vol.18 , pp. 81-87
- Réthore, M.-O.¹ Kaplan, J.-C.² Junien, C.L.³ Cruveiller, J.⁴ Dutrillaux, B.⁵ Aurias, A.⁶ Carpentier, S.⁷ Lafourcade, J.⁸ Lejeune, J.⁹

10
- 0015579613
- Identification of partial 12 trisomy by quinacrine fluorescence
- (1973) J. of Pediatr. , vol.82 , pp. 269-272
- Uchida, I.A.¹ Lin, C.C.²

11
- 0015503504
- Banding in human chromosomes treated with trypsin
- (1972) Nature New Bio. , vol.235 , pp. 52-53
- Wang, H.C.¹ Federoff, S.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.