Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Nuhad D. Dinno"'
Publikováno v:
Clinical Genetics. 19:51-54
A series of three infants with achondrogenesis, all born to the same mother, are reported. The third case was diagnosed in utero.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b130550ecc66f66e424d92209e6ece30
https://doi.org/10.1111/j.1399-0004.1981.tb00667.x
https://doi.org/10.1111/j.1399-0004.1981.tb00667.x
Autor:
Nuhad D. Dinno, R. S. Wappner, W. R. Breg, M. R. Seashore, E. L. Harris, Catherine G. Palmer, Bryan D. Hall
Publikováno v:
Clinical Genetics. 12:233-238
Four independently ascertained children who presented with unusual facies and delayed mental and physical development were found to have a similar deletion of part of the long arm of chromosome 7 (46,XX or XY, del(7)(q32); 46,XX or XY,del(7)(pter lea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85f0be6cc732984502b93cea7c1d52f9
https://doi.org/10.1111/j.1399-0004.1977.tb00932.x
https://doi.org/10.1111/j.1399-0004.1977.tb00932.x
Autor:
Nuhad D. Dinno
Publikováno v:
Pediatric Clinics of North America. 24:633-637
The pediatrician has a primary responsibility for the early detection of developmental problems. Attention is focused on high-risk predisposing factors aiding in early recognition of infants with developmental retardation or milder handicaps of educa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a910c0183b5a16d840b9b2df99c9b979
https://doi.org/10.1016/s0031-3955(16)33471-x
https://doi.org/10.1016/s0031-3955(16)33471-x
Publikováno v:
European Journal of Pediatrics. 123:39-42
We describe a female infant with lethal, short-limb dwarfism, micrognathia, hydrocephalus with occipital encephalocele and a generalized spondyloepimetaphyseal dysplasia who probably has the same condition that was described by Rolland et al. (1972)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a348f3a0ecf8494bdacff3035311983
https://doi.org/10.1007/bf00497678
https://doi.org/10.1007/bf00497678
Autor:
Bernard Weisskopf, Allan S. Bloom, Andrew W. Zimmerman, Robert M. Greenstein, Anabel Reese, Joseph H. Hersh, Nuhad D. Dinno
Publikováno v:
Developmental medicine and child neurology. 23(6)
Nine children with the "happy puppet" syndrome are presented here and 19 previously reported cases are reviewed. A characteristic psychological profile is suggested by the children's "unfocused" activities and inconsistent responsiveness to their sur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7de2627168e3b667df5dcb67ce644e1
https://pubmed.ncbi.nlm.nih.gov/7319144
https://pubmed.ncbi.nlm.nih.gov/7319144
Autor:
Kathleen S. Dale, Frank Yen, Joseph H. Hersh, Nuhad D. Dinno, Park S. Gerald, Bernard Weisskopf
Publikováno v:
American journal of diseases of children (1960). 139(1)
• A young woman with features resembling de Lange syndrome had a normal banded karyotype. Similar phenotypes were present in a maternal aunt and uncle. Utilizing high-resolution banding, the propositus was found to have a chromosomal abnormality ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ee10266bae129e2d41e64ccc4b58495
https://pubmed.ncbi.nlm.nih.gov/3969990
https://pubmed.ncbi.nlm.nih.gov/3969990
Publikováno v:
Clinical pediatrics. 13(3)
The cryptophthalmos-syndactyly syndrome is a rare disorder of which approximately 55 cases have been reported in the world literature. A few have been described in the American literature. It is the purpose of this paper to report another case and to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45e7aacc0a1a898ecd79fe63e708e64b
https://pubmed.ncbi.nlm.nih.gov/4360847
https://pubmed.ncbi.nlm.nih.gov/4360847
Publikováno v:
The Journal of Pediatrics. 99:325
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af2e1e8a1759a4c27fab3eb434819095
https://doi.org/10.1016/s0022-3476(81)80492-1
https://doi.org/10.1016/s0022-3476(81)80492-1
Publikováno v:
Pediatric Research. 15:561-561
We report two affected offspring with Osteogenesis Imperfecta, Type 2. The first child was born near term and expired shortly thereafter. Prenatal radiologic examination was consistent with O.I., Type 2. The second affected fetus was diagnosed at 19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8cc272c45d5732ac0d93649ab019b5d
https://doi.org/10.1203/00006450-198104001-00735
https://doi.org/10.1203/00006450-198104001-00735