RECURRENCE RISKS FOR RELATIVES IN FAMILIES WITH AN ISOLATED CASE OF THE FRAGILE X SYNDROME

被引：15

作者：

SHERMAN, SL

ROGATKO, A

TURNER, G

机构：

[1] MEM SLOAN KETTERING CANC CTR,DEPT EPIDEMIOL & BIOSTAT,NEW YORK,NY 10021

[2] PRINCE WALES HOSP,RANDWICK,NSW 2031,AUSTRALIA

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1988年 / 31卷 / 04期

关键词：

D O I：

10.1002/ajmg.1320310405

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：753 / 765

页数：13

共 12 条

[1] THE FRAGILE(X) SYNDROME - THE MUTATION PROBLEM [J].

JACOBS, PA ;

SHERMAN, S ;

TURNER, G ;

WEBB, T .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 23 (1-2) :611-617

[2]

LAIRD CD, 1987, GENETICS, V117, P587

[3]

MORTON NE, 1983, METHODS GENETIC EPID, P75

[4] FRAGILE-X TRANSMISSION AND THE DETERMINATION OF CARRIER PROBABILITIES FOR GENETIC-COUNSELING [J].

MULLEY, JC ;

SUTHERLAND, GR .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 26 (04) :987-990

[5]

NAVAJAS L, 1987, REV BRAS GENET, V10, P333

[6] RECOMBINATION AND AMPLIFICATION OF PYRIMIDINE-RICH SEQUENCES MAY BE RESPONSIBLE FOR INITIATION AND PROGRESSION OF THE XQ27 FRAGILE SITE - AN HYPOTHESIS [J].

NUSSBAUM, RL ;

AIRHART, SD ;

LEDBETTER, DH .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 23 (1-2) :715-721

[7] THE RECURRENCE RISKS FOR ISOLATED CASES WITH INCOMPLETELY PENETRANT X-LINKED CONDITIONS [J].

ROGATKO, A .

GENETIC EPIDEMIOLOGY, 1986, 3 (05) :357-364

[8] FURTHER SEGREGATION ANALYSIS OF THE FRAGILE-X SYNDROME WITH SPECIAL REFERENCE TO TRANSMITTING MALES [J].

SHERMAN, SL ;

JACOBS, PA ;

MORTON, NE ;

FROSTERISKENIUS, U ;

HOWARDPEEBLES, PN ;

NIELSEN, KB ;

PARTINGTON, MW ;

SUTHERLAND, GR ;

TURNER, G ;

WATSON, M .

HUMAN GENETICS, 1985, 69 (04) :289-299

[9] THE MARKER (X) SYNDROME - A CYTOGENETIC AND GENETIC-ANALYSIS [J].

SHERMAN, SL ;

MORTON, NE ;

JACOBS, PA ;

TURNER, G .

ANNALS OF HUMAN GENETICS, 1984, 48 (JAN) :21-37

[10]

STEVENSON AC, 1970, GENETIC COUNSELLING, P62

← 1 2 →