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Items: 17

1.

Chromosome polymorphism in American Negro and White populations.

Lubs HA, Ruddle FH.

Nature. 1971 Sep 10;233(5315):134-6. No abstract available.

PMID:
12058757
2.

Applications of comparative genomic hybridisation in constitutional chromosome studies.

Breen CJ, Barton L, Carey A, Dunlop A, Glancy M, Hall K, Hegarty AM, Khokhar MT, Power M, Ryan K, Green AJ, Stallings RL.

J Med Genet. 1999 Jul;36(7):511-7.

3.

Two unusual G-band variants of the short arm of chromosome 9.

Sutherland GR, Eyre H.

Clin Genet. 1981 May;19(5):331-4. No abstract available.

PMID:
7296923
4.

Prenatal diagnosis of an inherited translocation between chromosomes No. 9 and 18.

Ebbin AJ, Wilson MG, Towner JW, Slaughter JP.

J Med Genet. 1973 Mar;10(1):65-9. No abstract available.

5.

47, XY, t(9pplus;11qplus) in a mlae infant with multiple malformations.

Dinno ND, Silvey GL, Weisskopf B.

Clin Genet. 1974;6(2):125-31. No abstract available.

PMID:
4430152
6.

Structural variation in human nitotic chromosomes.

Leisti J.

Ann Acad Sci Fenn Biol. 1971;179:1-69. No abstract available.

PMID:
4261167
7.

Structural variation in chromosome No 9.

Madan K, Bobrow M.

Ann Genet. 1974 Jun;17(2):81-6. No abstract available.

PMID:
4139929
8.

A ring chromosome, diagnosed by quinacrine fluorescence as No. 9, in a mentally retarded girl.

Jacobsen P, Mikkelsen M, Rosleff F.

Clin Genet. 1973;4(5):434-41. No abstract available.

PMID:
4127395
9.

[Ring chromosome 9. Case report and review of the literature].

Manouvrier-Hanu S, Turck D, Gottrand F, Savary JB, Loeuille GA, Deminatti MM, Farriaux JP.

Ann Genet. 1988;31(4):250-3. French.

PMID:
3265311
10.

The prevalence of translocations in parents of children with regular trisomy 21: a possible interchromosomal effect?

Lindenbaum RH, Hultén M, McDermott A, Seabright M.

J Med Genet. 1985 Feb;22(1):24-8.

11.

Another case of ring chromosome 9 associated with gastroesophageal reflux.

Manouvrier-Hanu S, Turck D, Farriaux JP.

Am J Med Genet. 1989 Apr;32(4):558. No abstract available.

PMID:
2774007
12.

Pericentric inversion of chromosome 9 in prenatal diagnosis and infertility.

Uehara S, Akai Y, Takeyama Y, Takabayashi T, Okamura K, Yajima A.

Tohoku J Exp Med. 1992 Apr;166(4):417-27.

13.

Irregular phenotypic expression of ring chromosomes.

Zdansky R, Andrle M, Bühler E, Tsuchimoto T, Mayr WR, Rett A.

Humangenetik. 1975;26(3):193-8.

PMID:
1132877
14.

The 9p--syndrome.

Alfi OS, Donnell GN, Derencsenyi A.

Birth Defects Orig Artic Ser. 1976;12(5):157-60. No abstract available.

PMID:
953217
15.

The distal 9p trisomy syndrome: a major clinical-cytogenetic entity.

Centerwall WR.

Birth Defects Orig Artic Ser. 1977;13(3D):165-77. No abstract available.

PMID:
922135
16.

Trisomy 9p, a chromosome aberration with distinct radiologic findings.

Schinzel A.

Radiology. 1979 Jan;130(1):125-33.

PMID:
758640
17.

Complex de novo rearrangement of chromosome 9 with clinical features of monosomy 9p syndrome.

Hoo JJ, Parslow MI, Shaw RL, Veale AM.

Clin Genet. 1979 Sep;16(3):151-5.

PMID:
487636
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