Lin CC - Search Results

1

Selective IgA deficiency with 18q+ and 18q-- karyotypic anomalies.

Lewkonia RM, Lin CC, Haslam RH. Lewkonia RM, et al. Among authors: lin cc. J Med Genet. 1980 Dec;17(6):453-6. doi: 10.1136/jmg.17.6.453. J Med Genet. 1980. PMID: 6782212 Free PMC article.

2

Recurrent de novo interstitial deletion of 16q in two mentally retarded sisters.

Hoo JJ, Lowry RB, Lin CC, Haslam RH. Hoo JJ, et al. Among authors: lin cc. Clin Genet. 1985 Apr;27(4):420-5. doi: 10.1111/j.1399-0004.1985.tb02287.x. Clin Genet. 1985. PMID: 3995793

3

X-linked mental retardation with macro-orchidism and marker-X chromosomes.

Martin RH, Lin CC, Mathies BJ, Lowry RB. Martin RH, et al. Among authors: lin cc. Am J Med Genet. 1980;7(4):433-41. doi: 10.1002/ajmg.1320070405. Am J Med Genet. 1980. PMID: 6938132

4

Multiple, variable-sized, minute marker chromosomes.

Hoo JJ, Lin CC. Hoo JJ, et al. Among authors: lin cc. Am J Med Genet. 1988 Feb;29(2):361-3. doi: 10.1002/ajmg.1320290215. Am J Med Genet. 1988. PMID: 3354607 No abstract available.

5

Two cases of variant Philadelphia chromosome resulting from translocation (21;22) and (3;19;22).

Heikkila E, Lin CC, Hoo JJ. Heikkila E, et al. Among authors: lin cc. Cancer Genet Cytogenet. 1984 Feb;11(2):223-6. doi: 10.1016/0165-4608(84)90117-1. Cancer Genet Cytogenet. 1984. PMID: 6581860

6

A case of acute lymphoblastic leukemia with t(10;19)(q26;q13).

De Braekeleer M, Poon MC, Russell J, Lin CC. De Braekeleer M, et al. Among authors: lin cc. Cancer Genet Cytogenet. 1985 Apr 15;16(4):369-72. doi: 10.1016/0165-4608(85)90247-x. Cancer Genet Cytogenet. 1985. PMID: 3856474

7

DK phocomelia phenotype (von Voss-Cherstvoy syndrome) caused by somatic mosaicism for del(13q).

Bamforth JS, Lin CC. Bamforth JS, et al. Among authors: lin cc. Am J Med Genet. 1997 Dec 31;73(4):408-11. Am J Med Genet. 1997. PMID: 9415466 Review.

8

Terminal deletion of chromosome 10q at band 26.1: follow-up in an adolescent male with high-output renal failure from congenital obstructive uropathy.

Leonard NJ, Harley FL, Lin CC. Leonard NJ, et al. Among authors: lin cc. Am J Med Genet. 1999 Sep 10;86(2):115-7. Am J Med Genet. 1999. PMID: 10449644 Review.

9

The meiotic segregation of human sperm chromosomes in two men with accessory marker chromosomes.

Martin RH, Hildebrand KA, Yamamoto J, Peterson D, Rademaker AW, Taylor P, Lin CC. Martin RH, et al. Among authors: lin cc. Am J Med Genet. 1986 Oct;25(2):381-8. doi: 10.1002/ajmg.1320250225. Am J Med Genet. 1986. PMID: 3465241

10

Tertiary trisomy (22q11q),47,+der(22),t(11;22).

Biederman BM, Lin CC, Lowry RB, Somerville R. Biederman BM, et al. Among authors: lin cc. Hum Genet. 1980 Feb;53(2):173-7. doi: 10.1007/BF00273491. Hum Genet. 1980. PMID: 7358384

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