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Results of search for 'au:"PFEIFFER, R A"', page 7 of 14
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Authors
Ammermann, M
BACHMANN, K D
Baisch, C
Ballhausen, W G
Beinder, E
Bier, L
Büchner, T
Diekmann, L
Henkel, K E
KOSENOW, W
Kessel, E
Lenz, W
Majewski, F
PFEIFFER, R A
Pfeiffer, R A
Rauch, A
Rott, H D
Stöss, H
Trautmann, U
Ulmer, R
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Topics
Abnormalities, Multiple
Adolescent
Adult
Child
Child, Preschool
Chromosome Aberrations
Chromosome Disorders
Female
Humans
Infant
Infant, Newborn
Intellectual Disability
Karyotyping
Male
Pedigree
Pregnancy
Syndrome
Trisomy
abnormalities
genetics
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German
Your search returned 274 results.
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121.
[Reduplication behavior of chromosomes of group D (13-15) and identification of the extra-chromosome in trisomy D].
[electronic resource]
by
Büchner, T
Pfeiffer, R A
Stupperich, E
Producer:
19660723
In:
Klinische Wochenschrift
vol. 43
Online resources:
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122.
[The clinical aspects of trisomy of the X-chromosomes in adolescents (triple X-syndrome)].
[electronic resource]
by
Pfeiffer, R A
Palm, D
Jochmus, J
Producer:
19671002
In:
Monatsschrift fur Kinderheilkunde
vol. 115
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123.
[Gonadal tumors and intersexuality].
[electronic resource]
by
Legerlotz, C
Heidenreich, W
Pfeiffer, R A
Producer:
19710731
In:
Geburtshilfe und Frauenheilkunde
vol. 31
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124.
Genetic counseling of cleft sternum.
[electronic resource]
by
Kotzot, D
Huk, W
Pfeiffer, R A
Producer:
19941118
In:
Genetic counseling (Geneva, Switzerland)
vol. 5
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125.
[Chromosome anomalies in the blood cells of a child with multiple abnormalities].
[electronic resource]
by
PFEIFFER, R A
SCHELLONG, G
KOSENOW, W
Producer:
19981101
In:
Klinische Wochenschrift
vol. 40
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126.
Sagittal craniostenosis, congenital heart disease, mental deficiency and various dysmorphies in two sibs--a "new" syndrome?
[electronic resource]
by
Pfeiffer, R A
Singer, H
Zschiesche, S
Producer:
19870629
In:
European journal of pediatrics
vol. 146
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127.
[Unusual manifestations of neurofibromatosis (von Recklinghausen's disease) in childhood. Abdominal tumor with clitoris hypertrophy. Renal hypertension caused by renal artery stenosis. Monozygotic twins--plexiform neuroma in the head region and glaucoma].
[electronic resource]
by
Diekmann, L
Hüther, W
Pfeiffer, R A
Producer:
19680815
In:
Zeitschrift fur Kinderheilkunde
vol. 101
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128.
Extra chromosome in "cat eye" syndrome.
[electronic resource]
by
Pfeiffer, R A
Heimann, K
Heiming, E
Producer:
19700821
In:
Lancet (London, England)
vol. 1
Online resources:
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129.
[Problems of the XYY constitution].
[electronic resource]
by
Pfeiffer, R A
Riemer, G
Schneller, W
Producer:
19690427
In:
Die Medizinische Welt
vol. 2
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130.
Deletion or triplication of the alpha 3 (VI) collagen gene in three patients with 2q37 chromosome aberrations and symptoms of collagen-related disorders.
[electronic resource]
by
Rauch, A
Pfeiffer, R A
Trautmann, U
Producer:
19970122
In:
Clinical genetics
vol. 49
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131.
Pericentric inversions of the X chromosome. A new observation and review of the published cases.
[electronic resource]
by
Pfeiffer, R A
Kossakiewicz, M
Baisch, C
Producer:
19861118
In:
Journal de genetique humaine
vol. 34
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132.
Supernumerary chromosomes (trisomies) and maternal age.
[electronic resource]
by
Lenz, W
Pfeiffer, R A
Tünte, W
Producer:
19671020
In:
German medical monthly
vol. 12
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133.
[Autoradiographic labelling pattern of the chromosomes No. 1, 2, 3, 4, 5, 13-15, 16 and grade of conformity of homologues after incorporation of H3-thymidine during the late S phase. Quantitative studies of the cells of blood culture].
[electronic resource]
by
Büchner, T
Wilkens, A
Pfeiffer, R A
Producer:
19690214
In:
Klinische Wochenschrift
vol. 46
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134.
[The phenotype of the trisomy of the short arm of chromosome no. 4. (a new case with t (4p; 11q) (author's transl)].
[electronic resource]
by
Kessel, E
Pfeiffer, R A
Kosenow, W
Producer:
19760901
In:
Klinische Padiatrie
vol. 188
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135.
Clinical and molecular cytogenetic observations in three cases of "trisomy 12p syndrome".
[electronic resource]
by
Rauch, A
Trautmann, U
Pfeiffer, R A
Producer:
19960925
In:
American journal of medical genetics
vol. 63
Online resources:
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136.
Typical and partial cat eye syndrome: identification of the marker chromosome by FISH.
[electronic resource]
by
Liehr, T
Pfeiffer, R A
Trautmann, U
Producer:
19921202
In:
Clinical genetics
vol. 42
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137.
An unusual, possibly "new" MA/MR syndrome with sagittal craniosynostosis.
[electronic resource]
by
Pfeiffer, R A
Tietze, U
Welte, W
Producer:
19870629
In:
European journal of pediatrics
vol. 146
Online resources:
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138.
Acrocallosal syndrome in a child with de novo inverted tandem duplication of 12p11.2-p13.3.
[electronic resource]
by
Pfeiffer, R A
Legat, G
Trautmann, U
Producer:
19920723
In:
Annales de genetique
vol. 35
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139.
[The popliteal pterygium syndrome. A dominant autosomal malformation syndrome].
[electronic resource]
by
Pfeiffer, R A
Tünte, W
Reinken, M
Producer:
19710723
In:
Zeitschrift fur Kinderheilkunde
vol. 108
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140.
[Partial trisomy of the short arm of chromosome 4 due to translocation t(4p-22p+)].
[electronic resource]
by
Metz, F
Bier, L
Pfeiffer, R A
Producer:
19730926
In:
Humangenetik
vol. 18
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