Format
Sort by
Items per page

Send to

Choose Destination

Links from Books

Items: 20

1.

Tetrasomy 9q in an infant with cleft palate and multiple anomalies.

McPherson E, Neiswanger K, Surti U.

Clin Dysmorphol. 2005 Jul;14(3):145-7. Review.

PMID:
15930905
2.

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion.

Campuzano V, Montermini L, Moltò MD, Pianese L, Cossée M, Cavalcanti F, Monros E, Rodius F, Duclos F, Monticelli A, Zara F, Cañizares J, Koutnikova H, Bidichandani SI, Gellera C, Brice A, Trouillas P, De Michele G, Filla A, De Frutos R, Palau F, Patel PI, Di Donato S, Mandel JL, Cocozza S, Koenig M, Pandolfo M.

Science. 1996 Mar 8;271(5254):1423-7.

PMID:
8596916
3.

Extra G positive band on the long arm of chromosome 9.

Knight LA, Soon GM, Tan M.

J Med Genet. 1993 Jul;30(7):613.

4.

Constitutional heteromorphism of 9q13 --> q21 in a patient with chronic myelogenous leukemia.

Surana RB, Rafi SK, Christopher KL, Reid TJ, Weiss RB.

Clin Genet. 1995 Jun;47(6):321-3.

PMID:
7554367
5.

Case report of mosaic partial tetrasomy 9 mimicking Klinefelter syndrome.

Peters J, Pehl C, Miller K, Sandlin CJ.

Birth Defects Orig Artic Ser. 1982;18(3B):287-93. No abstract available.

PMID:
7139111
6.
7.

[Trisomy 9p : 2 further cases].

Turleau C, de Grouchy J, Chavin-Colin F, Roubin M, Langmaid H.

Ann Genet. 1974 Sep;17(3):167-74. French. No abstract available.

PMID:
4548817
8.

Four cases of 9p trisomy resulting from a balanced familial translocation (9:15) (q13;q11). Clinical picture and cytogenetic findings.

Zaremba J, Zdzienicka E, Glogowska I, Abramowicz T, Taracha B.

J Ment Defic Res. 1974 Jun;18(2):153-90. No abstract available.

PMID:
4141378
9.

[Giemsa-R-banding analysis of the trisomy 9p and report of a new case].

Rethoré MO, Hoehn H, Rott HD, Couturier J, Dutrillaux B, Lejeune J.

Humangenetik. 1973 Apr 16;18(2):129-38. French. No abstract available.

PMID:
4124236
10.

Balanced reciprocal translocations: risk factors for aneuploid segregant viability.

Davis JR, Rogers BB, Hagaman RM, Thies CA, Veomett IC.

Clin Genet. 1985 Jan;27(1):1-19. Review.

PMID:
3884190
11.
12.

Tetrasomy 9p caused by idic (9) (pter----q13----pter).

Cavalcanti DP, Ferrari I, de Almeida JC, de Pina Neto JM, de Oliveira JA.

Am J Med Genet. 1987 Jul;27(3):497-503.

PMID:
3631125
13.

Duplication of part of 9q due to maternal 12;9 inverted insertion associated with pyloric stenosis.

Yamamoto Y, Oguro N, Nara T, Horita H, Niitsu N, Imaizumi S.

Am J Med Genet. 1988 Oct;31(2):379-84. Review.

PMID:
2852899
14.

Euchromatic 9q + heteromorphism in a family.

Jalal SM, Kukolich MK, Garcia M, Day DW.

Am J Med Genet. 1990 Sep;37(1):155-6. No abstract available.

PMID:
2240035
15.

Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

Schinzel A, Hayashi K, Schmid W.

Humangenetik. 1975 Dec 23;30(4):307-16.

PMID:
1218860
16.

Physical and mental defect of chromosomal origin in four individuals of the same family. Trisomy for the short arm of 9.

Blank CE, Colver DC, Potter AM, McHugh J, Lorber J.

Clin Genet. 1975 Apr;7(4):261-73.

PMID:
1126048
17.

9p trisomy identified by Giemsa-11.

Wyandt HE, Hecht F, Magenis RE, Wysham DG, Prescott G.

Hum Genet. 1976 Mar 12;31(3):355-8.

PMID:
955631
18.

Trisomy 9p resulting from maternal 9/21 translocation.

Sŭbrt I, Blehová B, Pallová B.

Hum Genet. 1976 May 19;32(2):217-20.

PMID:
944684
19.

De novo trisomy 9pter leads to q13.

Kardon NB, Salwen HR, Krauss MA, Davis JG, Jenkins EC.

Hum Genet. 1977 Jun 30;37(2):149-53.

PMID:
885535
20.

Free trisomy 9P in elderly woman.

Gripenberg U, Hongell K, Iivanainen M, Kivimäki T.

Ann Genet. 1977 Mar;20(1):36-40.

PMID:
302671

Supplemental Content

Support Center