Mapping of a new locus for autosomal recessive nonsyndromic mental retardation in the chromosomal region 19p13.12-p13.2: further genetic heterogeneity.

被引：0

作者：

Basel-Vanagaite, L

Alkelai, A

Straussberg, R

Magal, N

Inbar, D

Mahagna, M

Shohat, M

机构：

[1] Rabin Med Ctr, Dept Med Genet, Petah Tiqwa, Israel

[2] Schneider Childrens Med Ctr Israel, Neurogenet Clin, Petah Tiqwa, Israel

[3] Felsenstein Med Res Ctr, Petah Tiqwa, Israel

[4] Tel Aviv Univ, Sackler Fac Med, IL-69978 Tel Aviv, Israel

[5] Schneider Childrens Med Ctr Israel, Neuropediat Unit, Petah Tiqwa, Israel

来源：

AMERICAN JOURNAL OF HUMAN GENETICS | 2003年 / 73卷 / 05期

关键词：

D O I：

暂无

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

1745

引用

页码：468 / 468

页数：1

共 15 条

[1] Mapping of a new locus for autosomal recessive non-syndromic mental retardation in the chromosomal region 19p13.12-p13.2: further genetic heterogeneity
Basel-Vanagaite, L
Alkelai, A
Straussberg, R
Magal, N
Inbar, D
Mahajna, M
Shohat, M
JOURNAL OF MEDICAL GENETICS, 2003, 40 (10) : 729 - 732
[2] Fine mapping of a locus for nonsyndromic mental retardation on chromosome 19p13
Nolan, D. K.
Chen, P.
Das, S.
Ober, C.
Waggoner, D.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2008, 146A (11) : 1414 - 1422
[3] DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13.2
Santos, Regie Lyn P.
Hassan, Muhammad Jawad
Sikandar, Shaheen
Lee, Kwanghyuk
Ali, Ghazanfar
Martin, Protacio E., Jr.
Wambangco, Michael Angelo L.
Ahmad, Wasim
Leal, Suzanne M.
HUMAN GENETICS, 2006, 120 (01) : 85 - 92
[4] DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13.2
Regie Lyn P. Santos
Muhammad Jawad Hassan
Shaheen Sikandar
Kwanghyuk Lee
Ghazanfar Ali
Protacio E. Martin
Michael Angelo L. Wambangco
Wasim Ahmad
Suzanne M. Leal
Human Genetics, 2006, 120 : 85 - 92
[5] Identification, by homozygosity mapping, of a novel locus for autosomal recessive congenital ichthyosis on chromosome 17p, and evidence for further genetic heterogeneity
Krebsová, A
Küster, W
Lestringant, GG
Schulze, B
Hinz, B
Frossard, PM
Reis, A
Hennies, HC
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (01) : 216 - 222
[6] A new locus for autosomal recessive non-syndromic mental retardation maps to 1p21.1-p13.3
Uyguner, O.
Kayserili, H.
Li, Y.
Karaman, B.
Nuernberg, G.
Hennies, H. C.
Becker, C.
Nuernberg, P.
Basaran, S.
Apak, M. Y.
Wollnik, B.
CLINICAL GENETICS, 2007, 71 (03) : 212 - 219
[7] Complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum: a new locus and further genetic heterogeneity
Boukhris, A.
Feki, I.
Elleuch, N.
Miladi, M. I.
Forlani, S.
Belal, S.
Brice, A.
Mhiri, C.
Stavanin, G.
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2009, 285 : S106 - S107
[8] The mapping of DFNB62, a new locus for autosomal recessive non-syndromic hearing impairment, to chromosome 12p13.2-p11.23
Ali, G
Santos, RLP
John, P
Wambangco, MAL
Lee, K
Ahmad, W
Leal, SM
CLINICAL GENETICS, 2006, 69 (05) : 429 - 433
[9] Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p-13.3-22.1.
Masmoudi, S
Tlili, A
Ghorbel, A
Chardenoux, S
Lemainque, A
Majava, M
Ben Zina, Z
Mala, J
Mannikko, M
Weil, D
Lathrop, M
Ala-Kokko, L
Drira, M
Petit, C
Ayadi, H
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 511 - 511
[10] Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1
Saber Masmoudi
Abdelaziz Tlili
Marja Majava
Abdel Monem Ghorbel
Sébastien Chardenoux
Arnaud Lemainque
Zeineb Ben Zina
Jihene Moala
Minna Männikkö
Dominique Weil
Mark Lathrop
Leena Ala-Kokko
Mohamed Drira
Christine Petit
Hammadi Ayadi
European Journal of Human Genetics, 2003, 11 : 185 - 188

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