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Results of search for 'au:"ROBINOW, M"', page 3 of 4
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Authors
Apesos, J
Armstrong, D
Armstrong, M D
Ashenhurst, E M
Atkinson, M
Babu, V R
Baker, D H
Bryant, J A
Chen, H
Edgerton, M T
Garn, S M
Johanson, A J
Johnson, G F
Kelly, T E
McKusick, V A
ROBINOW, M
Robinow, M
Roche, A F
SOBEL, E H
Shaw, A
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Topics
Abnormalities, Multiple
Adolescent
Adult
Child
Child, Preschool
Dwarfism
Female
Fingers
Humans
Infant
Infant, Newborn
Male
Pedigree
Radiography
Syndrome
abnormalities
complications
diagnosis
diagnostic imaging
genetics
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English
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41.
A pericentric inversion of a chromosome 4 with a t(4q+10p-) and a familial t(DqDq) in a mentally retarded girl.
[electronic resource]
by
Soukup, S W
Yarema, W
Robinow, M
Producer:
19750416
In:
Humangenetik
vol. 25
Online resources:
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42.
Femoral-facial syndrome--prenatal diagnosis--autosomal dominant inheritance.
[electronic resource]
by
Robinow, M
Sonek, J
Buttino, L
Veghte, A
Producer:
19951019
In:
American journal of medical genetics
vol. 57
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43.
Report on a disorder of the skeleton resembling rickets, associated with loss of teeth and deficient alkaline phosphatase activity in a 2-year-old child.
[electronic resource]
by
SOBEL, E H
CARK, L C
ROBINOW, M
Producer:
20040215
In:
A.M.A. American journal of diseases of children
vol. 83
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44.
Increments in handwrist ossification.
[electronic resource]
by
Garn, S M
Rohmann, C G
Robinow, M
Producer:
19981101
In:
American journal of physical anthropology
vol. 19
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45.
The genetic status of mothers of isolated cases of Duchenne muscular dystrophy.
[electronic resource]
by
Lane, R J
Robinow, M
Roses, A D
Producer:
19830623
In:
Journal of medical genetics
vol. 20
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46.
Syndactyly type V.
[electronic resource]
by
Robinow, M
Johnson, G F
Broock, G J
Producer:
19820826
In:
American journal of medical genetics
vol. 11
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47.
A newly recognized dwarfing syndrome.
[electronic resource]
by
Robinow, M
Silverman, F N
Smith, H D
Producer:
19690706
In:
American journal of diseases of children (1960)
vol. 117
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48.
Aicardi syndrome, papilloma of the choroid plexus, cleft lip, and cleft of the posterior palate.
[electronic resource]
by
Robinow, M
Johnson, G F
Minella, P A
Producer:
19840502
In:
The Journal of pediatrics
vol. 104
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49.
Distichiasis-lymphedema. A hereditary syndrome of multiple congenital defects.
[electronic resource]
by
Robinow, M
Johnson, G F
Verhagen, A D
Producer:
19700430
In:
American journal of diseases of children (1960)
vol. 119
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50.
The Lenz-Majewski hyperostotic dwarfism. A syndrome of multiple congenital anomalies, mental retardation, and progressive skeletal sclerosis.
[electronic resource]
by
Robinow, M
Johanson, A J
Smith, T H
Producer:
19771020
In:
The Journal of pediatrics
vol. 91
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51.
Turner syndrome: sonography showing fetal hydrops simulating hydramnios.
[electronic resource]
by
Robinow, M
Spisso, K
Buschi, A J
Brenbridge, A N
Producer:
19810219
In:
AJR. American journal of roentgenology
vol. 135
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52.
Autosomal recessive cerebellar hypoplasia and endosteal sclerosis: a newly recognized syndrome.
[electronic resource]
by
Charrow, J
Poznanski, A K
Unger, F M
Robinow, M
Producer:
19920228
In:
American journal of medical genetics
vol. 41
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53.
Intraventricular air and meconium-stained amniotic fluid from intrapartum rupture of myelomeningocele.
[electronic resource]
by
Robinow, M
Cavanaugh, D J
Bryant, J A
Long, D
Producer:
19831123
In:
AJNR. American journal of neuroradiology
vol. 4
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54.
Hereditary sclerosing poikiloderma.
[electronic resource]
by
Greer, K E
Weary, P E
Nagy, R
Robinow, M
Producer:
19780814
In:
International journal of dermatology
vol. 17
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55.
Hemifacial microsomia, ipsilateral facial palsy, and malformed auricle in two families: an autosomal dominant malformation.
[electronic resource]
by
Robinow, M
Reynolds, J F
FitzGerald, J
Bryant, J A
Producer:
19890323
In:
American journal of medical genetics. Supplement
vol. 2
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56.
Skeletal lesions following meningococcemia and disseminated intravascular coagulation. A recognizable skeletal dystrophy.
[electronic resource]
by
Robinow, M
Johnson, G F
Nanagas, M T
Mesghali, H
Producer:
19830324
In:
American journal of diseases of children (1960)
vol. 137
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57.
Rickets, deficiency of alkaline phosphatase activity and premature loss of teeth in childhood.
[electronic resource]
by
SOBEL, E H
CLARK, L C
FOX, R P
ROBINOW, M
Producer:
20030501
In:
Pediatrics
vol. 11
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58.
Robinow's syndrome. Partial primary hypogonadism in pubertal boys, with persistence of micropenis.
[electronic resource]
by
Lee, P A
Migeon, C J
Brown, T R
Robinow, M
Producer:
19820624
In:
American journal of diseases of children (1960)
vol. 136
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59.
Cerebral gigantism and thyrotoxicosis.
[electronic resource]
by
Wilson, T A
Neufeld, M R
Robinow, M
Johanson, A J
Producer:
19800530
In:
The Journal of pediatrics
vol. 96
Online resources:
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60.
New clinical aspects of hereditary mucoepithelial dysplasia.
[electronic resource]
by
Urban, M D
Schosser, R
Spohn, W
Wentling, W O
Robinow, M
Producer:
19910909
In:
American journal of medical genetics
vol. 39
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