Skip to main content
مکتبة رقمیه للعلوم الطبيه
Your cart is empty.
Cart
Lists
Your lists
Log in to create your own lists
Log in to your account
Your cookies
Search history
Search the catalog by:
Library catalog
Title
Author
Subject
ISBN
ISSN
Series
Call number
Search the catalog by keyword
Advanced search
Authority search
Tag cloud
Library
Log in to your account
Home
Advanced search
Results of search for 'au:"PFEIFFER, R A"', page 6 of 14
Refine your search
Availability
Limit to records with available items
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
Show more
Show less
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
Show more
Show less
Languages
English
French
German
Your search returned 274 results.
Sort
First
Previous
1
2
3
4
5
6
7
8
9
10
Next
Last
Sort by:
Relevance
Popularity (most to least)
Popularity (least to most)
Author (A-Z)
Author (Z-A)
Call number (0-9 to A-Z)
Call number (Z-A to 9-0)
Publication/Copyright date: Newest to oldest
Publication/Copyright date: Oldest to newest
Acquisition date: Newest to oldest
Acquisition date: Oldest to newest
Title (A-Z)
Title (Z-A)
Unhighlight
Highlight
Select all
Clear all
Select titles to:
Add to cart
Add to list
New list
Place hold
Results
101.
Present nosology of the Cenani-Lenz type of syndactyly.
[electronic resource]
by
Pfeiffer, R A
Meisel-Stosiek, M
Producer:
19820624
In:
Clinical genetics
vol. 21
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
102.
[Ring chromosome 8 (46,XY, 8 r) in a boy with debility (author's transl)].
[electronic resource]
by
Pfeiffer, R A
Lenard, H G
Producer:
19731214
In:
Klinische Padiatrie
vol. 185
Availability:
No items available.
Save to lists
Add to cart
(remove)
103.
["Crying cat", a new malformation syndrome as a sequel to a chromosome abnormality (deficiency of the short arm of chromosome No. 5)].
[electronic resource]
by
Pfeiffer, R A
Simon, H A
Producer:
19670129
In:
Munchener medizinische Wochenschrift (1950)
vol. 107
Availability:
No items available.
Save to lists
Add to cart
(remove)
104.
46,XX/46,XX,r(15) mosaiciam: report of a case.
[electronic resource]
by
Pfeiffer, R A
Dhadial, R
Lenz, W
Producer:
19770430
In:
Journal of medical genetics
vol. 14
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
105.
[Hypomelanosis cutis ITO (author's transl)].
[electronic resource]
by
Pfeiffer, R A
Happle, R
Stupperich, G
Producer:
19760706
In:
Klinische Padiatrie
vol. 188
Availability:
No items available.
Save to lists
Add to cart
(remove)
106.
[The Schwartz-Jampel syndrome (myotonia chondrodystrophica)].
[electronic resource]
by
Pfeiffer, R A
Bauer, H
Petersen, C
Producer:
19790629
In:
Helvetica paediatrica acta
vol. 32
Availability:
No items available.
Save to lists
Add to cart
(remove)
107.
A syndrome of short stature, amimic facies, enamel hypoplasia, slowly progressive stiffness of the joints and high-pitched voice in two siblings.
[electronic resource]
by
Pfeiffer, R A
Palm, D
Teller, W
Producer:
19780127
In:
The Journal of pediatrics
vol. 91
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
108.
Visualization of human somatic chromosomes by scanning electron microscopy.
[electronic resource]
by
Christenhuss, R
Büchner, T
Pfeiffer, R A
Producer:
19671219
In:
Nature
vol. 216
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
109.
[Asynchronous reduplication in length difference between homologous chromosomes A-1 in man].
[electronic resource]
by
Büchner, T
Wilkens, A
Pfeiffer, R A
Producer:
19670722
In:
Experimental cell research
vol. 46
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
110.
[Postaxial polydactyly: a symptom of partial trisomy of the long arm of chromosome 13. Two new observations with 46, XX, t (22;13) (q13;q31) and 46, XY, Dup (13) (pter-q34::q22-qter) (author's transl)].
[electronic resource]
by
Kessel, E
Pfeiffer, R A
Baisch, C
Producer:
19800523
In:
Klinische Padiatrie
vol. 192
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
111.
[Risk of repetition in families with a mongoloid child].
[electronic resource]
by
Pfeiffer, R A
Dhadial, R
Michelis, K
Producer:
19740114
In:
Monatsschrift fur Kinderheilkunde
vol. 121
Availability:
No items available.
Save to lists
Add to cart
(remove)
112.
[Fluorescent microscopy detection of human Y-chromosome in interphase nuclei using acridine derivatives ("atebrin", "acranil")].
[electronic resource]
by
Majewski, F
Bier, L
Pfeiffer, R A
Producer:
19711008
In:
Klinische Wochenschrift
vol. 49
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
113.
Single mandibular incisor in a patient with del (18p) anomaly.
[electronic resource]
by
Pfeiffer, R A
Hertrich, K
Cohen, M
Producer:
19950418
In:
Clinical genetics
vol. 46
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
114.
[Chromosomal research on blood cells of a patient with Waldenstrom's macroglobulinemia].
[electronic resource]
by
PFEIFFER, R A
KOSENOW, W
BAEUMER, A
Producer:
19981101
In:
Klinische Wochenschrift
vol. 40
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
115.
An autosomal recessive variant of spondylo-epiphyseal dysplasia in three sibs.
[electronic resource]
by
Pfeiffer, R A
Suess, J
Haagen, M
Producer:
19920915
In:
Pediatric radiology
vol. 22
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
116.
[The Hajdu-Cheney syndrome. The basilar impression as a diagnostic sign].
[electronic resource]
by
Laudi, B
Klinger, M
Pfeiffer, R A
Producer:
19910925
In:
Deutsche medizinische Wochenschrift (1946)
vol. 116
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
117.
[Familial translocation 22/Y and partial autosomal trisomy in a young girl].
[electronic resource]
by
Kessel, E
Pfeiffer, R A
Welling, P
Producer:
19791128
In:
Journal de genetique humaine
vol. 27
Availability:
No items available.
Save to lists
Add to cart
(remove)
118.
Tetraphocomelia and neonatal amegakaryocytic thrombocytopenia.
[electronic resource]
by
Pfeiffer, R A
Maintz, G
Haneke, C
Producer:
19730504
In:
Humangenetik
vol. 17
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
119.
Partial trisomy 14 following a balanced reciprocal translocation t(14q-;21q+).
[electronic resource]
by
Pfeiffer, R A
Büttinghaus, K
Struck, H
Producer:
19740528
In:
Humangenetik
vol. 20
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
120.
[Mohr and Claussen's syndrome (author's transl)].
[electronic resource]
by
Pfeiffer, R A
Majewski, F
Mannkopf, H
Producer:
19731214
In:
Klinische Padiatrie
vol. 185
Availability:
No items available.
Save to lists
Add to cart
(remove)
First
Previous
1
2
3
4
5
6
7
8
9
10
Next
Last