UNIQUE MOSAICISM IN PRADER-LABHART-WILLI SYNDROME - A CONTIGUOUS GENE OR ANEUPLOIDY SYNDROME

被引：19

作者：

KOUSSEFF, BG

DIAMOND, T

ESSIG, Y

MILLER, K

TEDESCO, T

机构：

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1987年 / 28卷 / 04期

关键词：

D O I：

10.1002/ajmg.1320280404

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：803 / 811

页数：9

共 22 条

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[J]. MEDICINE, 1983, 62 (02) : 59 - 80
[3] FAMILIAL PRADER-WILLI SYNDROME
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[J]. ARCHIVES OF INTERNAL MEDICINE, 1987, 147 (04) : 673 - 675
[4] DELETION OF CHROMOSOME-15 (Q11-13) IN A PRADER-LABHART-WILLI SYNDROME CLINIC POPULATION
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[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1984, 17 (02): : 485 - 495
[5] DEGROUCHY J, 1984, CLIN ATLAS HUMAN CHR, P270
[6] ISOLATION OF MOLECULAR PROBES ASSOCIATED WITH THE CHROMOSOME-15 INSTABILITY IN THE PRADER-WILLI SYNDROME
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[J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (12) : 4408 - 4412
[7] Fukui S., 1984, ADV BIOCHEM ENG BIOT, V29, P1, DOI DOI 10.1007/BFB0000689
[8] MOSAIC INVERSION DUPLICATION OF CHROMOSOME 15 WITHOUT PHENOTYPIC EFFECT - OCCURRENCE IN A FATHER AND DAUGHTER
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[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1984, 17 (03): : 649 - 654
[9] THE CYTOGENETIC CONTROVERSY IN THE PRADER-LABHART-WILLI SYNDROME
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[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1982, 13 (04): : 431 - 439
[10] KOUSSEFF BG, 1982, BIRTH DEFECTS-ORIG, V18, P301

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