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Results of search for 'au:"Roggenbuck, J"'
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Authors
Aref, P
Audlin, S
Baker, J
Blackman, V
Cutting, G R
Dugan, S
Dugan, S L
Ehrlich, M
Fikri, M
Fink, J M
Hefferon, T W
Herrera, D
Hu, J C-C
Jarvis, K
Liu, M
Mendelsohn, N J
Pond, D
Roggenbuck, J
Roggenbuck, J A
Temme, R
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Topics
Adaptation, Psychological
Adenosine
Adult
Amelogenesis Imperfecta
Animals
Attitude
Attitude of Health Personnel
Child
Exons
Female
Genetic Counseling
Humans
Infant
Male
Mutation
Phenotype
Prenatal Diagnosis
Trisomy
genetics
methods
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English
Your search returned 8 results.
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Results
1.
An experimental and theoretical study of the product distribution of the reaction CH2 (X 3B1) + NO.
[electronic resource]
by
Fikri, M
Meyer, S
Roggenbuck, J
Temps, F
Producer:
20020820
In:
Faraday discussions
no. 119
Online resources:
Available from publisher's website
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2.
Unique case of trisomy 2p24.3-pter with no associated monosomy.
[electronic resource]
by
Roggenbuck, J A
Fink, J M
Mendelsohn, N J
Producer:
20010712
In:
American journal of medical genetics
vol. 101
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No items available.
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3.
Perception of genetic risk among genetic counselors.
[electronic resource]
by
Roggenbuck, J
Olson, J E
Sellers, T A
Ludowese, C
Producer:
20030211
In:
Journal of genetic counseling
vol. 9
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4.
High frequencies of ICF syndrome-like pericentromeric heterochromatin decondensation and breakage in chromosome 1 in a chorionic villus sample.
[electronic resource]
by
Ehrlich, M
Tsien, F
Herrera, D
Blackman, V
Roggenbuck, J
Tuck-Muller, C M
Producer:
20020307
In:
Journal of medical genetics
vol. 38
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5.
The Long and Short of Genetic Counseling Summary Letters: A Case-control Study.
[electronic resource]
by
Roggenbuck, J
Temme, R
Pond, D
Baker, J
Jarvis, K
Liu, M
Dugan, S
Mendelsohn, N J
Producer:
20160307
In:
Journal of genetic counseling
vol. 24
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6.
Erratum to: The Long and Short of Genetic Counseling Letters: A Case-control Study.
[electronic resource]
by
Roggenbuck, J
Temme, R
Pond, D
Baker, J
Jarvis, K
Liu, M
Dugan, S
Mendelsohn, N J
Producer:
20160524
In:
Journal of genetic counseling
vol. 25
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7.
A synonymous mutation in TCOF1 causes Treacher Collins syndrome due to mis-splicing of a constitutive exon.
[electronic resource]
by
Macaya, D
Katsanis, S H
Hefferon, T W
Audlin, S
Mendelsohn, N J
Roggenbuck, J
Cutting, G R
Producer:
20090930
In:
American journal of medical genetics. Part A
vol. 149A
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8.
FAM20A mutations associated with enamel renal syndrome.
[electronic resource]
by
Wang, S K
Reid, B M
Dugan, S L
Roggenbuck, J A
Read, L
Aref, P
Taheri, A P H
Yeganeh, M Z
Simmer, J P
Hu, J C-C
Producer:
20140220
In:
Journal of dental research
vol. 93
Online resources:
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