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New observations on crossbilled hens. Heredity of dystrophy.
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作者
:
Mercier, L
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0
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0
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0
Mercier, L
Poisson, R
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0
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0
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0
Poisson, R
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来源
:
COMPTES RENDUS DES SEANCES DE LA SOCIETE DE BIOLOGIE ET DE SES FILIALES
|
1925年
/ 93卷
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D O I
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Q [生物科学];
学科分类号
:
07 ;
0710 ;
09 ;
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页码:1214 / 1217
页数:4
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[1]
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Sjoevall, Bertil
论文数:
0
引用数:
0
h-index:
0
Sjoevall, Bertil
[J].
ACTA PSYCHIATRICA ET NEUROLOGICA SUPPLEMENTUM,
1936,
(10):
: 7
-
239
[2]
Some observations on creatine formation in a case of progressive pseudohypertrophic muscular dystrophy.
Gibson, RB
论文数:
0
引用数:
0
h-index:
0
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State Univ Iowa, Dept Theory & Practice Med & Clin Med, Chem Res Lab, Dept Home Econ, Iowa City, IA USA
Gibson, RB
Martin, FT
论文数:
0
引用数:
0
h-index:
0
机构:
State Univ Iowa, Dept Theory & Practice Med & Clin Med, Chem Res Lab, Dept Home Econ, Iowa City, IA USA
Martin, FT
[J].
JOURNAL OF BIOLOGICAL CHEMISTRY,
1921,
49
(02)
: 319
-
326
[3]
Towards new mouse models for Duchenne Muscular Dystrophy.
Maatman, RGHJ
论文数:
0
引用数:
0
h-index:
0
机构:
Leiden Univ, Med Ctr, Dept Human & Clin Genet, Leiden, Netherlands
Maatman, RGHJ
de Meijer, EJ
论文数:
0
引用数:
0
h-index:
0
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Leiden Univ, Med Ctr, Dept Human & Clin Genet, Leiden, Netherlands
de Meijer, EJ
Heus, JJ
论文数:
0
引用数:
0
h-index:
0
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Heus, JJ
van Ommen, GJB
论文数:
0
引用数:
0
h-index:
0
机构:
Leiden Univ, Med Ctr, Dept Human & Clin Genet, Leiden, Netherlands
van Ommen, GJB
den Dunnen, JT
论文数:
0
引用数:
0
h-index:
0
机构:
Leiden Univ, Med Ctr, Dept Human & Clin Genet, Leiden, Netherlands
den Dunnen, JT
[J].
AMERICAN JOURNAL OF HUMAN GENETICS,
1999,
65
(04)
: A477
-
A477
[4]
Diagnosis, prenatal and of carriers, in families with Duchenne muscular dystrophy.: The introduction of new markers
Montejo-Pujadas, Y
论文数:
0
引用数:
0
h-index:
0
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Inst Neurol & Neurocirugia, Dept Neurogenet, Havana 10400, Cuba
Montejo-Pujadas, Y
Zaldívar-Vaillant, T
论文数:
0
引用数:
0
h-index:
0
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Inst Neurol & Neurocirugia, Dept Neurogenet, Havana 10400, Cuba
Zaldívar-Vaillant, T
Acevedo-López, AM
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Neurol & Neurocirugia, Dept Neurogenet, Havana 10400, Cuba
Inst Neurol & Neurocirugia, Dept Neurogenet, Havana 10400, Cuba
Acevedo-López, AM
Guerra-Badía, R
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Neurol & Neurocirugia, Dept Neurogenet, Havana 10400, Cuba
Inst Neurol & Neurocirugia, Dept Neurogenet, Havana 10400, Cuba
Guerra-Badía, R
[J].
REVISTA DE NEUROLOGIA,
2001,
33
(11)
: 1094
-
1095
[5]
SOME NEW OBSERVATIONS ON THE CLASSICAL LOGISTIC EQUATION WITH HEREDITY
FRANKEL, JI
论文数:
0
引用数:
0
h-index:
0
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UNIV CENT FLORIDA,DEPT MATH,ORLANDO,FL 32816
FRANKEL, JI
论文数:
引用数:
h-index:
机构:
CHOUDHURY, SR
[J].
APPLIED MATHEMATICS AND COMPUTATION,
1993,
58
(2-3)
: 275
-
308
[6]
Report of a new family with dominant congenital heredity stromal dystrophy of the cornea
Van Ginderdeuren, R
论文数:
0
引用数:
0
h-index:
0
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UZ Leuven, Dept Oogziekten, B-3000 Louvain, Belgium
Van Ginderdeuren, R
De Vos, R
论文数:
0
引用数:
0
h-index:
0
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De Vos, R
Casteels, I
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0
引用数:
0
h-index:
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Casteels, I
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论文数:
0
引用数:
0
h-index:
0
机构:
UZ Leuven, Dept Oogziekten, B-3000 Louvain, Belgium
Foets, B
[J].
CORNEA,
2002,
21
(01)
: 118
-
120
[7]
A new deletion in the ELOVL4 gene causes autosomal dominant Stargardt-like macular dystrophy and pattern dystrophy.
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0
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Bernstein, PS
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0
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Zabriskie, NA
Tammur, J
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0
引用数:
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0
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Univ Utah, Moran Eye Ctr, Salt Lake City, UT USA
Tammur, J
Hutchinson, A
论文数:
0
引用数:
0
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0
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Univ Utah, Moran Eye Ctr, Salt Lake City, UT USA
Hutchinson, A
Dixon, M
论文数:
0
引用数:
0
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0
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Univ Utah, Moran Eye Ctr, Salt Lake City, UT USA
Dixon, M
Peiffer, A
论文数:
0
引用数:
0
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Univ Utah, Moran Eye Ctr, Salt Lake City, UT USA
Peiffer, A
Zhang, K
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0
引用数:
0
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0
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Univ Utah, Moran Eye Ctr, Salt Lake City, UT USA
Zhang, K
Petrukhin, K
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Petrukhin, K
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Leppert, M
Allikmets, R
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Utah, Moran Eye Ctr, Salt Lake City, UT USA
Allikmets, R
[J].
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE,
2001,
42
(04)
: S323
-
S323
[8]
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Univ New Mexico, Sch Med, Albuquerque, NM 87131 USA
Univ New Mexico, Sch Med, Albuquerque, NM 87131 USA
Jaramillo, JS
Allen, RC
论文数:
0
引用数:
0
h-index:
0
机构:
Univ New Mexico, Sch Med, Albuquerque, NM 87131 USA
Univ New Mexico, Sch Med, Albuquerque, NM 87131 USA
Allen, RC
[J].
JOURNAL OF INVESTIGATIVE MEDICINE,
2004,
52
(01)
: S266
-
S266
[9]
New mutations in collagen VIα1, α2 genes cause autosomal dominant muscular dystrophy.
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论文数:
0
引用数:
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论文数:
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Univ Pittsburgh, Pittsburgh, PA USA
Gillanders, EM
Subramony, S
论文数:
0
引用数:
0
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0
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Univ Pittsburgh, Pittsburgh, PA USA
Subramony, S
Vedanarayayanan, V
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Pittsburgh, Pittsburgh, PA USA
Vedanarayayanan, V
Crowe, CA
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Pittsburgh, Pittsburgh, PA USA
Crowe, CA
Bingier, M
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Pittsburgh, Pittsburgh, PA USA
Bingier, M
Hoffman, EP
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Pittsburgh, Pittsburgh, PA USA
Hoffman, EP
[J].
AMERICAN JOURNAL OF HUMAN GENETICS,
1999,
65
(04)
: A112
-
A112
[10]
Revisiting X-linked Emery-Dreifuss muscular dystrophy. New insights into an old story
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论文数:
0
引用数:
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h-index:
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论文数:
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论文数:
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引用数:
0
h-index:
0
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Chikhaoui, K.
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论文数:
0
引用数:
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h-index:
0
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论文数:
0
引用数:
0
h-index:
0
机构:
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Kaplan, J. C.
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论文数:
0
引用数:
0
h-index:
0
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0
引用数:
0
h-index:
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论文数:
0
引用数:
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h-index:
0
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Grp Hosp Cochin, AP HP, Lab Biochim & Genet Mol, Paris, France
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Leturcq, F.
[J].
NEUROMUSCULAR DISORDERS,
2011,
21
(9-10)
: 673
-
673
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