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 5 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
81.
[Is there a syndrome of Ullrich and Feichtiger?(Author's transl)].
[electronic resource]
by
Pfeiffer, R A
Slavaykoff, H
Producer:
19750703
In:
Klinische Padiatrie
vol. 187
Availability:
No items available.
Save to lists
Add to cart
(remove)
82.
47,XY,+der(11;22)(q23;q12) following balanced translocation t(11;22)(q23;q12)mat. Remarks on the problem of trisomy 22.
[electronic resource]
by
Kessel, E
Pfeiffer, R A
Producer:
19770917
In:
Human genetics
vol. 37
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
83.
Evidence that activities of coagulation factors VII and X are linked to chromosome 13 (q34).
[electronic resource]
by
Ott, R
Pfeiffer, R A
Producer:
19840917
In:
Human heredity
vol. 34
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
84.
[The Aase syndrome: hereditary autosomal recessive congenital erythropoiesis insufficiency and triphalangeal thumbs].
[electronic resource]
by
Pfeiffer, R A
Ambs, E
Producer:
19830826
In:
Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde
vol. 131
Availability:
No items available.
Save to lists
Add to cart
(remove)
85.
Congenital universal alopecia, mental deficiency, and microcephaly in two sibs.
[electronic resource]
by
Pfeiffer, R A
Völklein, J
Producer:
19830119
In:
Journal of medical genetics
vol. 19
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
86.
Origin of 48,XXXY: the evidence of the Xg blood groups.
[electronic resource]
by
Pfeiffer, R A
Sanger, R
Producer:
19730831
In:
Journal of medical genetics
vol. 10
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
87.
[Sex-linked-dominant hereditary reduction in number of teeth].
[electronic resource]
by
Erpenstein, H
Pfeiffer, R A
Producer:
19680406
In:
Humangenetik
vol. 4
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
88.
Tandem duplication 11q23-ter in the dysmorphic child of a retarded mother mosaic for the same anomaly with no apparent abnormalities.
[electronic resource]
by
Pfeiffer, R A
Schütz, C
Producer:
19940328
In:
Annales de genetique
vol. 36
Availability:
No items available.
Save to lists
Add to cart
(remove)
89.
Mosaicism in three cases of 47, XY (or XX), +i(18)(p10) detected by interphase FISH of buccal mucosa.
[electronic resource]
by
Pfeiffer, R A
Schulze, T
Producer:
19950510
In:
Annales de genetique
vol. 37
Availability:
No items available.
Save to lists
Add to cart
(remove)
90.
Manifestation of heterozygosity in Papillon-Lefèvre syndrome?
[electronic resource]
by
Kotzot, D
Pfeiffer, R A
Producer:
19930601
In:
American journal of medical genetics
vol. 46
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
91.
[Genotype, chromosomes and chromatin findings in intersex states].
[electronic resource]
by
LENZ, W
PFEIFFER, R A
Producer:
19981101
In:
Geburtshilfe und Frauenheilkunde
vol. 23
Availability:
No items available.
Save to lists
Add to cart
(remove)
92.
[Prenatal ultrasonic diagnosis of achondroplasia].
[electronic resource]
by
Schlotter, C M
Pfeiffer, R A
Producer:
19851205
In:
Ultraschall in der Medizin (Stuttgart, Germany : 1980)
vol. 6
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
93.
[Microcephalic dwarfism associated with multiple dysplasias and early diabetes mellitus].
[electronic resource]
by
Pfeiffer, R A
Müller, K M
Producer:
19750818
In:
Journal de genetique humaine
vol. 22
Availability:
No items available.
Save to lists
Add to cart
(remove)
94.
An atypical case of Cockayne's syndrome.
[electronic resource]
by
Pfeiffer, R A
Bachmann, K D
Producer:
19730508
In:
Clinical genetics
vol. 4
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
95.
[Cerebral gigantism in childhood].
[electronic resource]
by
Schlack, H G
Pfeiffer, R A
Producer:
19720126
In:
Munchener medizinische Wochenschrift (1950)
vol. 112
Availability:
No items available.
Save to lists
Add to cart
(remove)
96.
Genetic nosology and counseling of humeroradial synostosis.
[electronic resource]
by
Pfeiffer, R A
Braun-Quentin, C
Producer:
19950209
In:
Genetic counseling (Geneva, Switzerland)
vol. 5
Availability:
No items available.
Save to lists
Add to cart
(remove)
97.
[STUDIES ON THE PROBLEM OF HAND RIDGES AND CONFIGURATIONS IN ABNORMALITIES OF THE EXTREMITIES].
[electronic resource]
by
PFEIFFER, R A
BERGEUS, Z U
Producer:
19961201
In:
Zeitschrift fur menschliche Vererbungs- und Konstitutionslehre
vol. 37
Availability:
No items available.
Save to lists
Add to cart
(remove)
98.
[The distribution of heterochromatin in human metaphase chromosomes].
[electronic resource]
by
Kim, M A
Pfeiffer, R A
Producer:
19720725
In:
Humangenetik
vol. 14
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
99.
Partial trisomy in a child with features suggesting mongolism.
[electronic resource]
by
Kumbnani, H K
Pfeiffer, R A
Producer:
19690930
In:
Journal of medical genetics
vol. 6
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
100.
Turner's syndrome in the male with chromosomal mosaicism.
[electronic resource]
by
Pfeiffer, R A
Pawlowitzki, I H
Producer:
19680303
In:
Humangenetik
vol. 4
Online resources:
Available from publisher's website
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