首页
学术期刊
论文检测
AIGC检测
热点
更多
数据
X-LINKED DYSOSTEOSCLEROSIS - 4 FAMILIAL CASES
被引:11
|
作者
:
PASCUALCASTROVIEJO, I
论文数:
0
引用数:
0
h-index:
0
机构:
CLIN INFANTIL LA PAZ,SERV NEUROL,MADRID,SPAIN
CLIN INFANTIL LA PAZ,SERV NEUROL,MADRID,SPAIN
PASCUALCASTROVIEJO, I
[
1
]
CASASFERNANDEZ, C
论文数:
0
引用数:
0
h-index:
0
机构:
CLIN INFANTIL LA PAZ,SERV NEUROL,MADRID,SPAIN
CLIN INFANTIL LA PAZ,SERV NEUROL,MADRID,SPAIN
CASASFERNANDEZ, C
[
1
]
LOPEZMARTIN, V
论文数:
0
引用数:
0
h-index:
0
机构:
CLIN INFANTIL LA PAZ,SERV NEUROL,MADRID,SPAIN
CLIN INFANTIL LA PAZ,SERV NEUROL,MADRID,SPAIN
LOPEZMARTIN, V
[
1
]
MARTINEZBERMEJO, A
论文数:
0
引用数:
0
h-index:
0
机构:
CLIN INFANTIL LA PAZ,SERV NEUROL,MADRID,SPAIN
CLIN INFANTIL LA PAZ,SERV NEUROL,MADRID,SPAIN
MARTINEZBERMEJO, A
[
1
]
机构
:
[1]
CLIN INFANTIL LA PAZ,SERV NEUROL,MADRID,SPAIN
来源
:
EUROPEAN JOURNAL OF PEDIATRICS
|
1977年
/ 126卷
/ 03期
关键词
:
D O I
:
10.1007/BF00442194
中图分类号
:
R72 [儿科学];
学科分类号
:
100202 ;
摘要
:
引用
收藏
页码:127 / 138
页数:12
相关论文
共 50 条
[41]
FAMILIAL X-LINKED MENTAL-RETARDATION AND MARKER X-CHROMOSOMES
JENNINGS, M
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV WASHINGTON,SCH MED,DEPT PEDIAT,SEATTLE,WA 98195
JENNINGS, M
HALL, JG
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV WASHINGTON,SCH MED,DEPT PEDIAT,SEATTLE,WA 98195
HALL, JG
HOEHN, H
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV WASHINGTON,SCH MED,DEPT PEDIAT,SEATTLE,WA 98195
HOEHN, H
PEDIATRIC RESEARCH,
1979,
13
(04)
: 420
-
420
[42]
Familial skewed X inactivation and X-linked mutations: Unbalanced X inactivation is a powerful means to ascertain X-linked genes that affect cell proliferation
Migeon, BR
论文数:
0
引用数:
0
h-index:
0
机构:
Johns Hopkins Univ, Sch Med, Dept Pediat, Baltimore, MD 21205 USA
Migeon, BR
Haisley-Royster, C
论文数:
0
引用数:
0
h-index:
0
机构:
Johns Hopkins Univ, Sch Med, Dept Pediat, Baltimore, MD 21205 USA
Haisley-Royster, C
AMERICAN JOURNAL OF HUMAN GENETICS,
1998,
62
(06)
: 1555
-
1557
[43]
Mutation in the norrie disease gene associated with one x-linked and four sporadic cases of familial exudative vitreoretinopathy
Shastry, BS
论文数:
0
引用数:
0
h-index:
0
机构:
OAKLAND UNIV,EYE RES INST,ROCHESTER,MI
Shastry, BS
Trese, MT
论文数:
0
引用数:
0
h-index:
0
机构:
OAKLAND UNIV,EYE RES INST,ROCHESTER,MI
Trese, MT
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE,
1996,
37
(03)
: 4576
-
4576
[44]
Familial skewed X inactivation and X-linked mutations: Unbalanced X inactivation is a powerful means to ascertain X-linked genes that affect cell proliferation - Reply
Hoffman, E
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Pittsburgh, Sch Med, Dept Mol Genet & Biochem, Pittsburgh, PA 15261 USA
Univ Pittsburgh, Sch Med, Dept Mol Genet & Biochem, Pittsburgh, PA 15261 USA
Hoffman, E
Pegoraro, E
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Pittsburgh, Sch Med, Dept Mol Genet & Biochem, Pittsburgh, PA 15261 USA
Univ Pittsburgh, Sch Med, Dept Mol Genet & Biochem, Pittsburgh, PA 15261 USA
Pegoraro, E
Lanasa, M
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Pittsburgh, Sch Med, Dept Mol Genet & Biochem, Pittsburgh, PA 15261 USA
Univ Pittsburgh, Sch Med, Dept Mol Genet & Biochem, Pittsburgh, PA 15261 USA
Lanasa, M
AMERICAN JOURNAL OF HUMAN GENETICS,
1998,
62
(06)
: 1557
-
1558
[45]
COLOCALIZATION OF X-LINKED AGAMMAGLOBULINEMIA AND X-LINKED IMMUNODEFICIENCY GENES
THOMAS, JD
论文数:
0
引用数:
0
h-index:
0
机构:
NIAID,IMMUNOL LAB,BETHESDA,MD 20892
THOMAS, JD
SIDERAS, P
论文数:
0
引用数:
0
h-index:
0
机构:
NIAID,IMMUNOL LAB,BETHESDA,MD 20892
SIDERAS, P
SMITH, CIE
论文数:
0
引用数:
0
h-index:
0
机构:
NIAID,IMMUNOL LAB,BETHESDA,MD 20892
SMITH, CIE
VORECHOVSKY, I
论文数:
0
引用数:
0
h-index:
0
机构:
NIAID,IMMUNOL LAB,BETHESDA,MD 20892
VORECHOVSKY, I
CHAPMAN, V
论文数:
0
引用数:
0
h-index:
0
机构:
NIAID,IMMUNOL LAB,BETHESDA,MD 20892
CHAPMAN, V
PAUL, WE
论文数:
0
引用数:
0
h-index:
0
机构:
NIAID,IMMUNOL LAB,BETHESDA,MD 20892
PAUL, WE
SCIENCE,
1993,
261
(5119)
: 355
-
358
[46]
FAMILIAL CYTOMEGALIC ADRENOCORTICAL HYPOPLASIA - AN X-LINKED SYNDROME OF PUBERTAL FAILURE
HAY, ID
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV GLASGOW,GLASGOW ROYAL INFIRM,DEPT MED,GLASGOW,SCOTLAND
HAY, ID
SMAIL, PJ
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV GLASGOW,GLASGOW ROYAL INFIRM,DEPT MED,GLASGOW,SCOTLAND
SMAIL, PJ
FORSYTH, CC
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV GLASGOW,GLASGOW ROYAL INFIRM,DEPT MED,GLASGOW,SCOTLAND
FORSYTH, CC
ARCHIVES OF DISEASE IN CHILDHOOD,
1981,
56
(09)
: 715
-
721
[47]
SECRETS IN THE FAMILY: XIAP VARIANT AND X-LINKED FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS
Ender, E.
论文数:
0
引用数:
0
h-index:
0
Ender, E.
Joshi, A.
论文数:
0
引用数:
0
h-index:
0
Joshi, A.
Ngo, T.
论文数:
0
引用数:
0
h-index:
0
Ngo, T.
ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY,
2023,
131
(05)
: S155
-
S155
[48]
FAMILIAL BAND HETEROTOPIAS - AN X-LINKED DOMINANT DISORDER WITH VARIABLE SEVERITY
SCHEFFER, IE
论文数:
0
引用数:
0
h-index:
0
SCHEFFER, IE
MITCHELL, LA
论文数:
0
引用数:
0
h-index:
0
MITCHELL, LA
HOWELL, RA
论文数:
0
引用数:
0
h-index:
0
HOWELL, RA
FITT, G
论文数:
0
引用数:
0
h-index:
0
FITT, G
SYNGENIOTIS, A
论文数:
0
引用数:
0
h-index:
0
SYNGENIOTIS, A
SALING, M
论文数:
0
引用数:
0
h-index:
0
SALING, M
BERKOVIC, SF
论文数:
0
引用数:
0
h-index:
0
BERKOVIC, SF
ANNALS OF NEUROLOGY,
1994,
36
(03)
: 511
-
511
[49]
FAMILIAL OCCURRENCE OF HETEROZYGOUS MANIFESTATIONS IN X-LINKED MUSCULAR-DYSTROPHIES
FALCAOCONCEICAO, DN
论文数:
0
引用数:
0
h-index:
0
FALCAOCONCEICAO, DN
PEREIRA, MDG
论文数:
0
引用数:
0
h-index:
0
PEREIRA, MDG
GONCALVES, MM
论文数:
0
引用数:
0
h-index:
0
GONCALVES, MM
BAPTISTA, ML
论文数:
0
引用数:
0
h-index:
0
BAPTISTA, ML
REVISTA BRASILEIRA DE GENETICA,
1983,
6
(03):
: 527
-
538
[50]
Familial thrombocytosis as a recessive, possibly X-linked trait in an Arab family
Stuhrmann, M
论文数:
0
引用数:
0
h-index:
0
机构:
Med Hsch Hannover, Inst Human Genet, D-30625 Hannover, Germany
Stuhrmann, M
Bashawri, L
论文数:
0
引用数:
0
h-index:
0
机构:
Med Hsch Hannover, Inst Human Genet, D-30625 Hannover, Germany
Bashawri, L
Ahmed, MA
论文数:
0
引用数:
0
h-index:
0
机构:
Med Hsch Hannover, Inst Human Genet, D-30625 Hannover, Germany
Ahmed, MA
Al-Awamy, BH
论文数:
0
引用数:
0
h-index:
0
机构:
Med Hsch Hannover, Inst Human Genet, D-30625 Hannover, Germany
Al-Awamy, BH
Kühnau, W
论文数:
0
引用数:
0
h-index:
0
机构:
Med Hsch Hannover, Inst Human Genet, D-30625 Hannover, Germany
Kühnau, W
Schmidtke, J
论文数:
0
引用数:
0
h-index:
0
机构:
Med Hsch Hannover, Inst Human Genet, D-30625 Hannover, Germany
Schmidtke, J
El-Harith, EA
论文数:
0
引用数:
0
h-index:
0
机构:
Med Hsch Hannover, Inst Human Genet, D-30625 Hannover, Germany
El-Harith, EA
BRITISH JOURNAL OF HAEMATOLOGY,
2001,
112
(03)
: 616
-
620
←
1
2
3
4
5
→