AUTOSOMAL-DOMINANT TRANSMISSION OF A GOLDENHAR-LIKE SYNDROME WITH LINKAGE TO THE BRANCHIOOTORENAL SYNDROME LOCUS AT 8Q13

被引：0
|
作者：
GRAHAM, JM [1 ]
HIXON, H [1 ]
BACINO, CA [1 ]
DAACKHIRSCH, S [1 ]
SEMINA, E [1 ]
MURRAY, JC [1 ]
机构：
[1] UNIV CALIF LOS ANGELES, CEDARS SINAI MED CTR, DIV DYSMORPHOL & CLIN GENET, LOS ANGELES, CA 90024 USA
来源：
PEDIATRIC RESEARCH | 1995年 / 37卷 / 04期
关键词：
D O I：
暂无
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
引用
收藏
页码：A83 / A83
页数：1
相关论文
共 50 条
  • [31] Weill-Marchesani syndrome - Possible linkage of the autosomal dominant form to 15q21.1
    Wirtz, MK
    Samples, JR
    Kramer, PL
    Rust, K
    Yount, J
    Acott, TS
    Koler, RD
    Cisler, J
    Jahed, A
    Gorlin, RJ
    Godfrey, M
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1996, 65 (01): : 68 - 75
  • [32] Refinement of a locus for a distinct syndrome of autosomal dominant cleft lip and palate to 2q35
    Winter, RM
    Prescott, NJ
    Lees, MM
    Malcolm, S
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2002, 10 : 218 - 219
  • [33] Nonsense mutations in FZD2 cause autosomal-dominant omodysplasia: Robinow syndrome-like phenotypes
    Nagasaki, Keisuke
    Nishimura, Gen
    Kikuchi, Toru
    Nyuzuki, Hiromi
    Sasaki, Sunao
    Ogawa, Yohei
    Saitoh, Akihiko
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2018, 176 (03) : 739 - 742
  • [34] A novel autosomal dominant restless legs syndrome locus maps to chromosome 20p13
    Levchenko, A.
    Provost, S.
    Montplaisir, J.
    Xiong, L.
    St-Onge, J.
    Thibodeau, P.
    Rivière, J.
    Desautels, A.
    Turecki, G.
    Dubé, M.
    Rouleau, G. A.
    MOVEMENT DISORDERS, 2006, 21 : S413 - S413
  • [35] A novel autosomal dominant restless legs syndrome locus maps to chromosome 20p13
    Levchenko, A.
    Provost, S.
    Montplaisir, J. -Y.
    Xiong, L.
    St-Onge, J.
    Thibodeau, P.
    Riviere, J. -B.
    Desautels, A.
    Turecki, G.
    Dube, M. -P.
    Rouleau, G. A.
    NEUROLOGY, 2006, 67 (05) : 900 - 901
  • [36] AUTOSOMAL-DOMINANT TRANSMISSION OF TRICHO-RHINO-PHALANGEAL SYNDROME - REPORT OF 4 UNRELATED FAMILIES, REVIEW OF 60 CASES
    GIEDION, A
    BURDEA, M
    FRUCHTER, Z
    MELONI, T
    TROSC, V
    HELVETICA PAEDIATRICA ACTA, 1973, 28 (03) : 249 - 259
  • [37] Genetic and physical mapping of the locus for autosomal dominant renal Fanconi syndrome, on chromosome 15q15.3
    Lichter-Konecki, U
    Broman, KW
    Blau, EB
    Konecki, DS
    AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (01) : 264 - 268
  • [38] A PROPOSED NEW CONTIGUOUS GENE SYNDROME ON 8Q CONSISTS OF BRANCHIOOTORENAL (BOR) SYNDROME, DUANE SYNDROME, A DOMINANT FORM OF HYDROCEPHALUS AND TRAPEZE APLASIA - IMPLICATIONS FOR THE MAPPING OF THE BOR GENE
    VINCENT, C
    KALATZIS, V
    COMPAIN, S
    LEVILLIERS, J
    SLIM, R
    GRAIA, F
    PEREIRA, MD
    NIVELON, A
    CROQUETTE, MF
    LACOMBE, D
    VIGNERON, J
    HELIAS, J
    BROYER, M
    CALLEN, DF
    HAAN, EA
    WEISSENBACH, J
    LACROIX, B
    BELLANECHANTELOT, C
    LEPASLIER, D
    COHEN, D
    PETIT, C
    HUMAN MOLECULAR GENETICS, 1994, 3 (10) : 1859 - 1866
  • [39] A COMPLETE AUTOSOMAL-DOMINANT TRIPHALANGEAL THUMB POLYSYNDACTYLY SYNDROME IN A LARGE INDIAN FAMILY MAPS TO CHROMOSOME 7Q36
    RHADAKRISHNA, U
    BLOUIN, JL
    SOLANKI, JV
    DHORIANI, GM
    ANTONARAKIS, SE
    AMERICAN JOURNAL OF HUMAN GENETICS, 1995, 57 (04) : 1155 - 1155
  • [40] LINKAGE MAPPING OF ONE FORM (RP1) OF AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA TO 8Q11-Q21 AND EXCLUSION OF CANDIDATE GENES
    SADLER, LA
    BLANTON, SH
    COTTINGHAM, RA
    CRAFT, CM
    SWAROOP, A
    WAGNER, MJ
    HECKENLIVELY, JR
    DAIGER, SP
    AMERICAN JOURNAL OF HUMAN GENETICS, 1993, 53 (03) : 1065 - 1065
12345