Alain VERLOES
机构: Professeur de Génétique, Faculté de Médecine , Université de Paris
每年引用次数
引用次数
引用: 27,990
H-指数: 88
I10-指数 : 343
出版物: 695
Monosomy 11q: Report of Two Familial Cases and Review of the Literature
Roland Hustinx , Alian Verloes , Bettina Grattagliano , Christian Herens
American Journal of Medical Genetics 47 ( 3) 312 -317
16
1993
CFC syndrome: a syndrome distinct from Noonan syndrome.
J. Kaplan , M. Le Merrer , A. Berloes , J. Rigo
Annales De Genetique 31 ( 4) 230 -234
24
1988
Combined 10pter-->p11 and 18pter-->q11 trisomy in a 7-year-old child.
A. Verloes , L. Van Maldergem , L. Koulischer , Y. Gillerot
Genetic Counseling 3 ( 3) 155 -159
2
1992
Roberts-sc Phocomelia Syndrome With Exencephaly
A. Verloes , P. Dodinval , Mc. Retz , L. Vanmaldergem
Annales De Genetique 32 ( 3) 169 -170
2
1989
Sponastrime dysplasia with mental retardation: A distinct entity
A. Verloes , Jean-Marie Dubru , Jean-Paul Misson , P. Jamblin
1994
Phenotypic variability in Van der Woude syndrome
A. Verloes , J. F. Chateil , D. Fontan , D. Lacombe
Genetic Counseling 6 ( 3) 221 -226
25
1995
Neuroblastoma in a dwarfed newborn. Possible clue to the chromosomal localization of the gene for achondroplasia
A. Verloes , J. P. Paquot , V. Jossa , L. Koulischer
Annales De Genetique 34 ( 1) 25 -26
1991
Les techniques récentes de procréation médicalement assistée et le conseil génétique
S. Lesenfants , M. Jamar , C. Herens , A. Verloes
Andrologie 8 ( 3) 321 -328
1998
Syndrome typique de l'hydantoïne chez un enfant de mère non épileptique
A. Verloes , G. Pierquin , C. Lambotte
Presse Medicale 15 ( 36)
1986
Les polyendocrinopathies : aspects diagnostiques et thérapeutiques
A. Beckers , M. Meurisse , O. Louis , A. Verloes
Medecine Et Hygiene 53 ( 2082) 1613 -1617
1995
A dominantly inherited syndrome with frontonasal malformation Variant of Teebi hypertelorism syndrome or new entity
A. Verloes , C. Baumann
American Journal of Human Genetics 71(4 Suppl.) 267
2002
Phenotypic spectrum associated with SPECC1L pathogenic variants: new families and critical review of the nosology of Teebi, Opitz GBBB, and Baraitser-Winter syndromes
A Verloes , D Haye , A Toutain , D Bonneau
European Journal of Human Genetics 27 1517 -1518
2019
Aspondylodysostosis Delineation of a probably recessive spinal dysosotosis with absent ossification of all vertebral bodies
A. Verloes , M. Gonzales , P. Maroteaux , J. L. Taillemitte
American Journal of Human Genetics 73 ( 5) 261
2003
A Long-term Competent Chimeric Immune System in a Dizygotic Dichorionic Twin
V. Biran , M. Bornes , A. Aboura , S. Masmoudi
Pediatrics 128 ( 2)
8
2011
Le point sur le syndrome de Bardet-Biedl
H. Dollfus , A. Verloes , D. Bonneau , M. Cossée
Journal Francais D Ophtalmologie 28 ( 1) 106 -112
8
2005
375 Dermoïde conjonctivo-limbique et Syndrome de Delleman
J.N. Serpe , I. Ssi Yan Kai , P. Rapp , A. Verloes
Journal Francais D Ophtalmologie 30
2007
Simplified gyral pattern in severe developmental microcephalies? New insights from allometric modeling for spatial and spectral analysis of gyrification
D. Germanaud , J. Lefèvre , C. Fischer , M. Bintner
NeuroImage 102 ( 2) 317 -331
20
2014
Bardet-biedl syndrome and brain abnormalities.
C. Rooryck , S. Pelras , J.-F. Chateil , C. Cances
Neuropediatrics 38 ( 1) 5 -9
31
2007
Plasma amino acid concentrations in term infants fed human milk, a whey-predominant formula, or a whey hydrolysate formula
J. Rigo , A. Verloes , J. Senterre
The Journal of Pediatrics 115 ( 5) 752 -755
35
1989
RASopathies et cancers de l’enfant
M. Strullu , A. Caye , A. Verloes , H. Cavé
Revue d'Oncologie Hématologie Pédiatrique 3 ( 4) 188 -196
2015