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Items: 1 to 20 of 22

1.

Amniocentesis before 14 completed weeks as an alternative to transabdominal chorionic villus sampling: a controlled trial with infant follow-up.

Nagel HT, Vandenbussche FP, Keirse MJ, Oepkes D, Oosterwijk JC, Beverstock G, Kanhai HH.

Prenat Diagn. 1998 May;18(5):465-75.

PMID:
9621380
2.
4.

Partial monosomy 10q and partial trisomy 9q with anal atresia due to maternal translocation: t(9;10)(q32;q26).

Tsukuda T, Nagata I, Sawada H, Murakami J, Hanaki K, Urashima H, Kaneda T, Shimizu N, Kaibara N, Kodama N, Ohzeki T, Shiraki K.

Clin Genet. 1996 Oct;50(4):220-2.

PMID:
9001803
5.

Dinucleotide repeat polymorphism on chromosome 9q32.

Toda T, Ikegawa S, Miyake M, Nakahori Y, Nakamura Y.

Jpn J Hum Genet. 1995 Dec;40(4):333-4.

PMID:
8851767
6.

Partial trisomy 9q due to maternal 9/17 translocation.

Aftimos SF, Hoo JJ, Parslow MI.

Am J Dis Child. 1980 Sep;134(9):848-50.

PMID:
7416109
7.
8.

Partial trisomy 9q resulting from a familial translocation t(9;16)(q32;q24).

Soltan HC, Jung JH, Pyatt Z, Singh RP.

Clin Genet. 1984 May;25(5):449-54.

PMID:
6723106
9.
10.

Paracentric inversions in man.

Madan K, Seabright M, Lindenbaum RH, Bobrow M.

J Med Genet. 1984 Dec;21(6):407-12. Review.

12.
13.

Cytogenetic analysis of 688 couples experiencing multiple spontaneous abortions.

Castle D, Bernstein R.

Am J Med Genet. 1988 Mar;29(3):549-56.

PMID:
3376998
14.

Cytogenetic study of 1,633 cases.

Wang SG, Ren GQ, Xue H, Shen QY, Song LL, Yuan P.

Chin Med J (Engl). 1988 Apr;101(4):231-6. No abstract available.

PMID:
3138079
15.
17.

Fragile X testing in a diagnostic cytogenetics laboratory.

Voullaire LE, Webb GC, Leversha M.

J Med Genet. 1989 Jul;26(7):439-42.

19.

Schizophrenia and mental retardation in an adult male with a de novo interstitial deletion 9(q32q34.1).

Park JP, Moeschler JB, Berg SZ, Wurster-Hill DH.

J Med Genet. 1991 Apr;28(4):282-3.

20.

Patients with deletions of 9q22q34 do not define a syndrome: three case reports and a literature review.

Farrell SA, Siegel-Bartelt J, Teshima I.

Clin Genet. 1991 Sep;40(3):207-14. Review.

PMID:
1773536
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